1
|
Chen X, Zhang Y, Huang Z, Bi B, Wang X. Identification and functional analysis of proteins in Anabarilius grahami at different growth stages based on 4D-DIA quantitative proteomics technology. Food Chem 2025; 482:144053. [PMID: 40187310 DOI: 10.1016/j.foodchem.2025.144053] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/31/2024] [Revised: 03/03/2025] [Accepted: 03/24/2025] [Indexed: 04/07/2025]
Abstract
This study compared the proteome of Anabarilius grahami at three growth stages with Carassius auratus at a single growth stage to identify and analyze protein functions in A. grahami using quantitative proteomics technology. A total of 1821 proteins were identified, among which six differentially abundant proteins (DAPs) were found as biomarkers for discriminating C. auratus and A. grahami. Additionally, seven DAPs were identified as factors that could discriminate A. grahami at the three growth stages studied. Furthermore, aspartate aminotransferase and alanine transaminase were identified as key enzymes involved in the synthesis of glutamic acid and aspartic acid, while very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase and CXXC motif containing zinc-binding protein were associated with the synthesis of polyunsaturated fatty acids. These findings provide deeper insights into the nutritional and functional properties of proteins in A. grahami, offering theoretical significance for the utilization of its protein resources and the development of A. grahami related products.
Collapse
Affiliation(s)
- Xiaoshan Chen
- College of Food Science & Technology, Yunnan Agricultural University, Kunming 650201, Yunnan, China
| | - Yaxuan Zhang
- College of Food Science & Technology, Yunnan Agricultural University, Kunming 650201, Yunnan, China
| | - Zhiyuan Huang
- College of Food Science & Technology, Yunnan Agricultural University, Kunming 650201, Yunnan, China
| | - Baoliang Bi
- International College, Yunnan Agricultural University, Kunming 650201, Yunnan, China.
| | - Xuefeng Wang
- College of Food Science & Technology, Yunnan Agricultural University, Kunming 650201, Yunnan, China.
| |
Collapse
|
2
|
Huether KM, Lamb JM, Skelly J, Brigham E, McCormack MC, Bose S, Garrow OJ, Dixon AE. Omega-3 fatty acid intake potentiates bronchodilator response in patients with obesity and poorly controlled asthma. Respir Med 2025; 243:108131. [PMID: 40294806 DOI: 10.1016/j.rmed.2025.108131] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/04/2024] [Revised: 04/14/2025] [Accepted: 04/25/2025] [Indexed: 04/30/2025]
Abstract
RATIONALE Obesity is linked to poorly controlled asthma and may impair bronchodilator response. This study examines dietary factors affecting asthma symptoms, control, and lung function. METHODS In a multi-center, cross-sectional study of 102 individuals with obesity and poorly controlled asthma, we assessed dietary intake (Arizona Food Frequency Questionnaire), asthma symptoms and control (standardized questionnaires), and lung function (spirometry and bronchodilator response). Correlations between omega-3 and -6 fatty acids with asthma outcomes and lung function were examined using Pearson correlations and multivariate regression. RESULTS Median age was 56 (IQR 41-64) years, and median BMI was 37 (35-42) kg/m2. Fifty-four percent were African American and 75 % were female. Median total calorie intake was 2029 (1199-3837) kcal, median total omega-3 intake was 1.07 (0.63-2.04) g, and median omega-6 intake was 24.54 (13.31-45.35) g. No significant relationship was found between fatty acid intake and asthma symptoms, asthma control, or baseline lung function. However, percent bronchodilator response was positively correlated with omega-3 fatty acids (r = 0.273, p = 0.0074). After adjusting for caloric intake, for every 1 g increase in omega-3 intake, there was a 4 % increase in percent bronchodilator response. CONCLUSIONS Dietary intake of omega-3 fatty acids may influence bronchodilator response in patients with poorly controlled asthma and obesity. Interventions to improve overall dietary quality, such as increased omega-3 intake, may improve medication response in people with obesity and poorly controlled asthma. Future research is needed to better understand this association and determine if additional dietary factors might affect medication responses.
Collapse
Affiliation(s)
| | | | | | | | - Meredith C McCormack
- Center for Clinical Trials, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
| | - Sonali Bose
- Icahn School of Medicine, New York, NY, USA.
| | | | | |
Collapse
|
3
|
Gaižauskaitė Ž, Klavins L, Almonaityte K. Optimised extraction of bioactive compounds from spruce needles for sustainable applications. WASTE MANAGEMENT (NEW YORK, N.Y.) 2025; 201:114784. [PMID: 40209445 DOI: 10.1016/j.wasman.2025.114784] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Subscribe] [Scholar Register] [Received: 02/18/2025] [Revised: 03/18/2025] [Accepted: 04/02/2025] [Indexed: 04/12/2025]
Abstract
Besides bark and branches, coniferous needles contribute to approximately 30 % of the biomass left unused in forests after timber harvesting, posing fire and environmental risks. However, by extracting valuable compounds from spruce needles, such as proanthocyanidins, phenolic compounds, shikimic acid, and others, targeted use of forestry by-product biomass can be achieved. Given the consumer demand for natural products and the growing need for alternative preservatives to ensure food safety, it is imperative that plant-derived components be fully assessed for their feasibility for food application. In this work extraction conditions for spruce needles were optimized using Response Surface Methodology, to obtain extracts with the highest concentration of bioactive compounds. The main identified and optimized extraction variables were temperature and time. Using the optimal extraction conditions allowed to extract a maximum concentration of phenolic compounds (79.21 ± 0.21 mgGAE/g DM), proanthocyanidins (21.70 ± 0.24 mgCE/g DM) and shikimic acid (32.4 ± 0.1 mg/g DM). Additionally, vitamins B6 and B9, in maximum concentration of 3.7 ± 0.14 µg/g DM and 4.35 ± 0.05 mg/g DM were obtained, respectively. The macro- and micro-nutrient composition of the extract obtained under optimal conditions was determined and the antibacterial characteristics against gram-positive food pathogens such as Staphylococcus aureus, Bacillus cereus, Listeria monocytogenes, were determined. Due to its rich composition of bioactive compounds, this extract stands out not only as a valuable and safe solution for use in sustainable food but can also be applied in the pharmaceutical field.
Collapse
Affiliation(s)
- Žydrūnė Gaižauskaitė
- Food Institute, Kaunas University of Technology, Radvilenu Rd.19 C, Kaunas, LT 50254, Lithuania
| | - Linards Klavins
- Department of Environmental Science, University of Latvia, Raina Blvd. 19, LV-1586 Riga, Latvia
| | - Karolina Almonaityte
- Food Institute, Kaunas University of Technology, Radvilenu Rd.19 C, Kaunas, LT 50254, Lithuania.
| |
Collapse
|
4
|
Paya H, Hosseinzadeh M, Taghizadeh A, Hosseinkhani A, Hasanpur K, Besharati M, Palangi V, Harzand MM, Lackner M. Different sources of fat in starter and its effect on growth performance, blood parameters and immune system of calves. Vet Anim Sci 2025; 28:100451. [PMID: 40276078 PMCID: PMC12020867 DOI: 10.1016/j.vas.2025.100451] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/26/2025] Open
Abstract
Calf rearing from birth to weaning is a critical and sensitive period in dairy farming, as it determines the future of a herd. The aim of this work was to investigate the effects of different fat sources on growth performance, immune response and rumen and blood parameters in suckling calves. Forty female Holstein calves (average weight 40 kg, body score 3) were studied from birth to weaning (3 to 75 days). A completely randomized design with 4 treatments (10 replicates each) was used: i) control (no fat source), ii) coconut oil (2 % saturated fat), iii) flaxseed oil (2 % linoleic acid), and iv) safflower oil (2 % linoleic acid). Calf performance was evaluated weekly and feces were examined daily. Rumen parameters (volatile fatty acids and pH), blood parameters (glucose, protein, urea and cholesterol) and immune response (white and red blood cells and immunoglobulin G) were assessed at the end of the trial. According to the results, the highest feed intake after 10 weeks was recorded in the safflower oil treatment, which differed significantly from the control treatment (p < 0.05). The highest weight gain of calves fed diets containing unsaturated fats was observed in the 8th, 9th and 10th weeks, which was significantly higher than in the control and treatment containing coconut oil (p < 0.05). The height of experimental calves was affected by fats, except in the 1st and 2nd weeks. The experimental treatments were not significantly different in terms of fecal scores during the entire experimental period (p > 0.05). The effect of the experimental treatments was not significantly dependent on the pH of the calves' rumen fluid during the experimental period. The total volatile fatty acid content was significantly affected by the treatment (p < 0.01) at the end of the experimental period. Blood parameters (glucose, protein and urea), red blood cells and immunoglobulin G of the calves were significantly affected by the treatment (p < 0.05). The results of this study show that the use of different fat sources, especially those with unsaturated fatty acids containing linoleic and linolenic acid, in the starter diet of calves improved growth performance, immune response and rumen/blood parameters in female Holstein calves compared to the other groups.
Collapse
Affiliation(s)
- Hamid Paya
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Mojtaba Hosseinzadeh
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Akbar Taghizadeh
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Ali Hosseinkhani
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Karim Hasanpur
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Maghsoud Besharati
- Department of Animal Science, Ahar Faculty of Agriculture and Natural Resources, University of Tabriz, Tabriz, Iran
| | - Valiollah Palangi
- Visiting Researcher at Department of Life Sciences, Western Caspian University, Baku, Azerbaijan
| | - Mehri Montazer Harzand
- Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
| | - Maximilian Lackner
- Department of Industrial Engineering, University of Applied Sciences Technikum Wien, Hoechstaedtplatz 6, 1200, Vienna, Austria
| |
Collapse
|
5
|
Koçyiğit E, Gövez NE, Arslan S, Ağagündüz D. A narrative review on dietary components and patterns and age-related macular degeneration. Nutr Res Rev 2025; 38:143-170. [PMID: 38221852 DOI: 10.1017/s0954422424000015] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/16/2024]
Abstract
Age-related macular degeneration (AMD) is one of the most prevalent eye diseases among the ageing population worldwide. It is a leading cause of blindness in individuals over 55, particularly in industrialised Western countries. The prevalence of AMD increases with age, and genetic factors and environmental influences are believed to contribute to its development. Among the environmental factors, diet plays a significant role in AMD. This review explores the association between dietary components, dietary patterns and AMD. Various nutrients, non-nutrient substances and dietary models that have the potential to counteract oxidative stress and inflammation, which are underlying mechanisms of AMD, are discussed. Consuming fruits, vegetables, fish and seafood, whole grains, olive oil, nuts and low-glycaemic-index foods has been highlighted as beneficial for reducing the risk of AMD. Adhering to the Mediterranean diet, which encompasses these elements, can be recommended as a dietary pattern for AMD. Furthermore, the modulation of the gut microbiota through dietary interventions and probiotics has shown promise in managing AMD.
Collapse
Affiliation(s)
- Emine Koçyiğit
- Department of Nutrition and Dietetics, Ordu University, Ordu, Türkiye
| | - Nazlıcan Erdoğan Gövez
- Department of Nutrition and Dietetics, Faculty of Health Sciences, Gazi University, Ankara, Türkiye
| | - Sabriye Arslan
- Department of Nutrition and Dietetics, Faculty of Health Sciences, Gazi University, Ankara, Türkiye
| | - Duygu Ağagündüz
- Department of Nutrition and Dietetics, Faculty of Health Sciences, Gazi University, Ankara, Türkiye
| |
Collapse
|
6
|
Chen L, Tan T, Wu Q, Cui F, Chen Y, Chen H, Zhao Y, Xiang X, Shan Z, Tang Y, Deng Q. Dietary polyunsaturated fatty acid and risk of gout: a cohort study integrating genetic predisposition and metabolomics. Eur J Epidemiol 2025:10.1007/s10654-025-01242-9. [PMID: 40426003 DOI: 10.1007/s10654-025-01242-9] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/13/2025] [Accepted: 04/28/2025] [Indexed: 05/29/2025]
Abstract
OBJECTIVES Gout is the most common inflammatory arthritis and affects quality of life. Dietary polyunsaturated fatty acids (PUFAs) have protective effects against various diseases, but its role in gout remains uncertain. Our study aims to assess the association between PUFAs intake and gout risk, the role of genetic factors, and the possible impact of metabolites. METHODS This study included 198,033 participants who were free of gout at baseline and completed at least one reliable dietary assessment in the UK Biobank. Cox proportional hazard models were used to estimate the associations between PUFAs intake and gout risk, and the modified effects of genetic predisposition. Mediation analysis also explored the mediating role of metabolic signature in associations between specific PUFAs intake and gout. RESULTS Over a median follow-up of 9.47 years, 1,708 incident cases of gout were recorded. Gout risk was significantly associated with the second quartile of linoleic acid (LA) (0.86 [0.75, 1.00]) intake and the highest quartiles of alpha-linolenic acid (ALA) (0.72 [0.62, 0.84]), total PUFA (HR: 0.84 [95% CI:0.71, 0.99]), n-6 PUFA (0.84 [0.71, 0.99]), n-3 PUFA (0.83 [0.71, 0.98]), and eicosapentaenoic acid (EPA) (0.79 [0.68, 0.91]), compared to the lowest quartiles. We observed joint effects of PUFAs intake and genetic susceptibility on gout risk. Mediation analysis showed that high-density lipoprotein (HDL) and triglycerides mediated the associations of ALA and LA with gout risk. CONCLUSION Our findings suggested the potential benefits of PUFAs in reducing gout risk, particularly vegetable sources, with HDL and triglycerides as key mediators.
Collapse
Affiliation(s)
- Li Chen
- Hubei Key Laboratory of Lipid Chemistry and Nutrition, Key Laboratory of Oilseeds Processing, Ministry of Agriculture, Oil Crops and Lipids Process Technology National & Local Joint Engineering Laboratory, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, 430062, Hubei, China
| | - Tianqi Tan
- Institute of Maternal and Child Health, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430015, China
| | - Qi Wu
- Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Laboratory of Environment Health (Incubation), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China
| | - Feipeng Cui
- Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Laboratory of Environment Health (Incubation), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China
| | - Yashu Chen
- Hubei Key Laboratory of Lipid Chemistry and Nutrition, Key Laboratory of Oilseeds Processing, Ministry of Agriculture, Oil Crops and Lipids Process Technology National & Local Joint Engineering Laboratory, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, 430062, Hubei, China
| | - Huimin Chen
- Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Laboratory of Environment Health (Incubation), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China
| | - Ying Zhao
- School of Public Health, Kunming Medical University, Kunming, 650500, China
| | - Xia Xiang
- Hubei Key Laboratory of Lipid Chemistry and Nutrition, Key Laboratory of Oilseeds Processing, Ministry of Agriculture, Oil Crops and Lipids Process Technology National & Local Joint Engineering Laboratory, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, 430062, Hubei, China
| | - Zhilei Shan
- Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Laboratory of Environment Health (Incubation), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
| | - Yuhan Tang
- Department of Nutrition and Food Hygiene, Hubei Key Laboratory of Food Nutrition and Safety, Ministry of Education Key Laboratory of Environment and Health and MOE Key Lab of Environment and Health, Key Laboratory of Environment and Health (Wuhan), Ministry of Environmental Protection, State Key Laboratory of Environment Health (Incubation), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
| | - Qianchun Deng
- Hubei Key Laboratory of Lipid Chemistry and Nutrition, Key Laboratory of Oilseeds Processing, Ministry of Agriculture, Oil Crops and Lipids Process Technology National & Local Joint Engineering Laboratory, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan, 430062, Hubei, China.
| |
Collapse
|
7
|
Hong SW, Heydari A, Watson PR, Teesdale-Spittle PH, Page R, Northcote PT, Keyzers RA, Vyssotski M, Truman P. Potent inhibition of human monoamine oxidase A and B by phenolic compounds and polyunsaturated fatty acids in tobacco smoke. Chem Biol Interact 2025; 413:111477. [PMID: 40088998 DOI: 10.1016/j.cbi.2025.111477] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/15/2024] [Revised: 08/29/2024] [Accepted: 03/12/2025] [Indexed: 03/17/2025]
Abstract
Smoking is a main cause of premature death and preventable disease in the world. Interestingly, animal studies indicate that inhibition of monoamine oxidase (MAO), key enzymes for the degradation of neurotransmitters, increased self-administration of nicotine. The purpose of this study was to identify and characterize the potential MAO inhibitors in tobacco smoke responsible for MAO inhibition in smokers. A bioassay-guided isolation from an extract of tobacco smoke showed that catechol, 4-methylcatechol, hydroquinone, α-linolenic acid, and linoleic acid all displayed potent human MAO inhibitory activity. Additionally, the tobacco catechols 4-ethylcatechol and 4-vinylcatechol were included to test their inhibitory potencies. Catechol, 4-methylcatechol, 4-ethylcatechol, and hydroquinone are potent and irreversible MAO inhibitors. Among the phenolic compounds tested, 4-methylcatechol and 4-ethylcatechol inhibited MAO A with IC50 values of 10.0 and 12.6 μM, respectively, reducing to 0.27 and 0.43 μM after 1 h preincubation. In addition, α-linolenic acid and linoleic acid competitively inhibited MAO A with Ki values of 10.50 and 6.95 μM, respectively. These results suggest that MAO inhibition by phenolics and polyunsaturated fatty acids in tobacco smoke may be important contributors to the MAO inhibition experienced by smokers and to the enhancement of nicotine dependence this MAO inhibition is believed to cause.
Collapse
Affiliation(s)
- Sa Weon Hong
- School of Health Sciences, Massey University, Wellington, 6021, New Zealand.
| | - Ali Heydari
- School of Health Sciences, Massey University, Wellington, 6021, New Zealand
| | - Paris R Watson
- School of Health Sciences, Massey University, Wellington, 6021, New Zealand
| | - Paul H Teesdale-Spittle
- School of Biological Sciences, Victoria University of Wellington, Wellington, 6012, New Zealand
| | - Rachel Page
- School of Health Sciences, Massey University, Wellington, 6021, New Zealand
| | - Peter T Northcote
- Ferrier Research Institute, Victoria University of Wellington, Wellington, 6012, New Zealand
| | - Robert A Keyzers
- School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, 6012, New Zealand
| | - Mikhail Vyssotski
- Callaghan Innovation, Gracefield Innovation Quarter, Lower Hutt, 5010, New Zealand
| | - Penelope Truman
- School of Health Sciences, Massey University, Wellington, 6021, New Zealand; Institute of Environmental Science and Research Ltd, Porirua, 5022, New Zealand
| |
Collapse
|
8
|
Hachem M, Ali AH, Hejou M, Almansoori A, Abulhassan S, Hussein F, Khalifa R, Khalifa R, Corridon PR. Sustainable and biotechnological production of docosahexaenoic acid from marine protists and slaughterhouse waste. Crit Rev Biotechnol 2025:1-18. [PMID: 40414819 DOI: 10.1080/07388551.2025.2499895] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/10/2023] [Revised: 04/15/2025] [Accepted: 04/20/2025] [Indexed: 05/27/2025]
Abstract
Docosahexaenoic acid (DHA, 22:6n-3) is an essential omega-3 polyunsaturated fatty acid, abundant in the brain and eyes. DHA is crucial for maintaining the structural integrity and physiological functions of these vital organs. Within the brain, DHA is concentrated in the gray matter, synaptic membranes, and hippocampus. Likewise, in the eyes, substantial quantities can be found in the retina, with lower levels in the cornea and lens. Previous studies have outlined the potential for culturing marine heterotrophic protists in ways that provide cost-effective and sustainable DHA biosynthesis. Similarly, our previous work on repurposing slaughterhouse waste has highlighted this underutilized source of brain and ocular tissue, which can support the extraction of valuable nutrients such as DHA. In this review, we will examine the current state of the art related to DHA production from these two sources, explore potential applications, and outline the possible benefits that may be generated from our approaches, with an emphasis on ocular diseases.
Collapse
Affiliation(s)
- Mayssa Hachem
- Department of Chemistry, College of Engineering and Physical Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
- Food Technology and Security Research Center, Khalifa University of Sciences and Technology, Abu Dhabi, United Arab Emirates
- Healthcare Engineering Innovation Group, Khalifa University of Sciences and Technology, Abu Dhabi, United Arab Emirates
| | - Abdelmoneim H Ali
- Department of Food Science, College of Agriculture and Veterinary Medicine, United Arab Emirates University (UAEU), Al Ain, United Arab Emirates
| | - Mariam Hejou
- Department of Biomedical Engineering and Biotechnology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Aliyaa Almansoori
- Department of Immunology and Physiology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Shamma Abulhassan
- Department of Immunology and Physiology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Fatimah Hussein
- Department of Biomedical Engineering and Biotechnology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Rana Khalifa
- Department of Biomedical Engineering and Biotechnology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Rayan Khalifa
- Department of Biomedical Engineering and Biotechnology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| | - Peter R Corridon
- Healthcare Engineering Innovation Group, Khalifa University of Sciences and Technology, Abu Dhabi, United Arab Emirates
- Department of Biomedical Engineering and Biotechnology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
- Department of Immunology and Physiology, College of Medicine and Health Sciences, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
- Center for Biotechnology, Khalifa University of Science and Technology, Abu Dhabi, United Arab Emirates
| |
Collapse
|
9
|
Zhang X, Guan F, Gou W, Wang Q, Du S, Su C, Zhang J, Zheng JS, Wang H, Zhang B. Multi-trajectories of BMI, waist circumference, gut microbiota, and incident dyslipidemia: a 27-year prospective study. mSystems 2025; 10:e0024325. [PMID: 40293249 PMCID: PMC12090771 DOI: 10.1128/msystems.00243-25] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/17/2025] [Accepted: 03/31/2025] [Indexed: 04/30/2025] Open
Abstract
Evidence is insufficient to establish a longitudinal association between combined trajectories of body mass index (BMI) and waist circumference (WC) and dyslipidemia. This study investigated the associations between multi-trajectories of BMI and WC over 24 years and the subsequent risk of dyslipidemia in a large cohort of 10,678 Chinese adults from the China Health and Nutrition Survey. Utilizing a group-based trajectory model, we identified four distinct trajectories: normal, normal-increasing, overweight-increasing, and obesity-increasing. Our results indicated that ascending trajectories of BMI and WC are significantly associated with increased odds of dyslipidemia, particularly in males, with odds ratios (OR) of 2.10, 2.69, and 3.56 for the normal-increasing, overweight-increasing, and obesity-increasing groups, respectively. Among females, the normal-increasing group exhibited a significant increased risk (OR: 1.54). Furthermore, we explored the gut microbiota associated with these trajectories, identifying 3, 8, and 4 bacterial genera linked to increasing BMI and WC in males, alongside two genera in females with the normal-increasing trajectory. We identified a total of 23, 25, and 10 differential metabolites significantly associated with these genera, except for Group 2 in males. The inclusion of relevant microbiome and metabolite data improved the model's predictive capacity for the risk of dyslipidemia, with ROC values increasing from 0.655 to 0.875. Our findings underscore the critical implications of continuous weight gain on metabolic health and suggest that gut microbiota may play a pivotal role in understanding these associations.IMPORTANCEEmerging evidence suggests a close connection between the gut microbiome and both human obesity and dyslipidemia, suggesting that the gut microbiome may play an important role in the obesity-dyslipidemia relationship. In this study, we observed several characteristic genera, including Clostridium_sensu_stricto_1, Turicibacter, and CHKCI002 among males and Parabacteroides and [Eubacterium]_brachy_group among females, which were negatively associated with high-risk trajectories. They were also related to free fatty acids (FFAs) and oxidized lipid metabolites. These shared and unique gut microbial and metabolic signatures among combined trajectories of BMI and WC with a higher risk of dyslipidemia could provide important evidence for the omics mechanism pathway of long-term obesity trend leading to dyslipidemia.
Collapse
Affiliation(s)
- Xiaofan Zhang
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| | - Fangxu Guan
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| | - Wanglong Gou
- Zhejiang Key Laboratory of Multi-Omics in Infection and Immunity, Center for Infectious Disease Research, School of Medicine, Westlake University School of Medicine, Hangzhou, Zhejiang, China
| | - Qi Wang
- Chaoyang District of Beijing Centre for Disease Control and Prevention, Beijing, China
| | - Shufa Du
- Department of Nutrition and Carolina Population Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
| | - Chang Su
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| | - Jiguo Zhang
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| | - Ju-Sheng Zheng
- Zhejiang Key Laboratory of Multi-Omics in Infection and Immunity, Center for Infectious Disease Research, School of Medicine, Westlake University School of Medicine, Hangzhou, Zhejiang, China
- Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, China
| | - Huijun Wang
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| | - Bing Zhang
- National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing, China
- Key Laboratory of Public Nutrition and Health, National Health Commission of the People’s Republic of China, Beijing, China
| |
Collapse
|
10
|
Daboussi I, Fehri NE, Contò M, Castrica M, Bejaoui S, Quattrone A, Ferchichi MA, Amraoui M, Tibaoui S, Curone G, Vigo D, Menchetti L, Dal Bosco A, Andoni E, Brecchia G, Failla S, Jemmali B. Growth Performance, Carcass Traits and Meat Quality in Rabbits Fed with Two Different Percentages of Extruded Linseed. Foods 2025; 14:1778. [PMID: 40428557 DOI: 10.3390/foods14101778] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/29/2025] [Revised: 05/07/2025] [Accepted: 05/15/2025] [Indexed: 05/29/2025] Open
Abstract
This study evaluated the effect of two levels of extruded linseed (EL) in the diet on growth performance, carcass yield, and meat quality of growing rabbits. Sixty-nine New Zealand White male rabbits (Oryctolagus cuniculus) were assigned after weaning to three dietary groups: control (C), 2.5% EL (L2.5%), and 5% EL (L5%). At the end of the fattening period (from 37 to 93 days of age), rabbits were slaughtered. EL supplementation significantly reduced average daily weight gain (ADG) in the L5% group (p < 0.05), while other performance parameters were not significantly affected. Meat from the L5% group exhibited a higher fat content (p < 0.001) and lower water-holding capacity (p < 0.05) compared to the others. The fatty acid profile showed a significant increase in n-3 polyunsaturated fatty acids (PUFAs) and a decrease in n-6 PUFA (p < 0.05), resulting in a markedly reduced n-6/n-3 ratio (p < 0.001) in supplemented groups. EL supplementation also enhanced long-chain n-3 PUFA levels, particularly docosapentaenoic acid (DPA). Although lipid oxidation was slightly increased (p < 0.05), sensory attributes remained unaffected. These findings support EL supplementation as a nutritional strategy to increase the n-3 fatty acids in rabbit meat without compromising physical and sensory quality.
Collapse
Affiliation(s)
- Imen Daboussi
- Institut National Agronomique de Tunis, Université de Carthage, Tunisie, 43 Av. Charles Nicolle, Tunis 1082, Tunisia
| | - Nour Elhouda Fehri
- Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy
| | - Michela Contò
- Consiglio per la Ricerca in Agricoltura e l'Analisi Dell'Economia Agraria (CREA), Research Centre for Animal Production and Aquaculture, Via Salaria 31, 00015 Rome, Italy
| | - Marta Castrica
- Comparative Biomedicine and Food Science, University of Padova, Agripolis, Viale dell'Univesità 16, 35020 Legnaro, Italy
| | - Safa Bejaoui
- Laboratory of Integrated Improvement and Development of Animal Productivity and Food Resources LR13AGR02, Mateur Higher School of Agriculture, University of Carthage, Mateur 7030, Tunisia
| | - Alda Quattrone
- Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy
| | - Mohamed Amine Ferchichi
- Laboratory of Integrated Improvement and Development of Animal Productivity and Food Resources LR13AGR02, Mateur Higher School of Agriculture, University of Carthage, Mateur 7030, Tunisia
| | - Marouen Amraoui
- Laboratory of Integrated Improvement and Development of Animal Productivity and Food Resources LR13AGR02, Mateur Higher School of Agriculture, University of Carthage, Mateur 7030, Tunisia
| | - Souha Tibaoui
- Laboratory of Integrated Improvement and Development of Animal Productivity and Food Resources LR13AGR02, Mateur Higher School of Agriculture, University of Carthage, Mateur 7030, Tunisia
| | - Giulio Curone
- Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy
| | - Daniele Vigo
- Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy
| | - Laura Menchetti
- School of Biosciences and Veterinary Medicine, University of Camerino, Via Circonvallazione 93/95, 62024 Matelica, Italy
| | - Alessandro Dal Bosco
- Department of Agricultural, Environmental and Food Science, University of Perugia, Borgo XX Giugno 74, 06124 Perugia, Italy
| | - Egon Andoni
- Faculty of Veterinary Medicine, Agricultural University of Tirana, Kodër Kamëz, 1029 Tirana, Albania
| | - Gabriele Brecchia
- Department of Veterinary Medicine and Animal Sciences, University of Milan, Via dell'Università 6, 26900 Lodi, Italy
| | - Sebastiana Failla
- Consiglio per la Ricerca in Agricoltura e l'Analisi Dell'Economia Agraria (CREA), Research Centre for Animal Production and Aquaculture, Via Salaria 31, 00015 Rome, Italy
| | - Bayrem Jemmali
- Laboratory of Integrated Improvement and Development of Animal Productivity and Food Resources LR13AGR02, Mateur Higher School of Agriculture, University of Carthage, Mateur 7030, Tunisia
| |
Collapse
|
11
|
Yu Y, Fu R, Jin C, Gao H, Han L, Qi M, Fu B, Li Q, Wang Y, Cheng Y, Leng J. Ruminal microbiome-host metabolome crosstalk in the synthesis of unsaturated fatty acids in buffalo milk. J Dairy Sci 2025:S0022-0302(25)00360-1. [PMID: 40383389 DOI: 10.3168/jds.2024-26176] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/04/2025] [Accepted: 04/24/2025] [Indexed: 05/20/2025]
Abstract
Interactions between rumen microorganisms and their metabolites contribute to milk yield and milk fat content in dairy cows. However, whether rumen microbes and host metabolism affect fatty acid synthesis in milk is unknown. In this study, we investigated the potential regulatory mechanisms affecting the unsaturated fatty acid content of Binglangjiang buffalo by using macrogenomics and metabolomics. Macrogenomic analysis showed that Bacteroides was significantly more abundant in the high UFA group (HF), contributing to the improvement of functions related to fatty acid synthesis. Then, we found that the rumen microbiota of the HF group was enriched in 2 important pathways involved in lipid metabolism (i.e., fatty acid biosynthesis and fatty acid metabolism), suggesting that more fatty acids were synthesized in the HF group. Metabolomics analyses showed that most of the UFA were more abundant in the HF group, which was also confirmed by the quantification of related metabolic pathways in milk fatty acids, suggesting that the HF group has a higher capacity to synthesize MUFA and PUFA. Correlation analysis of rumen lipid metabolic pathways and metabolites revealed that metabolic pathways such as fatty acid biosynthesis, fatty acid metabolism, metabolic pathways, and peroxisome proliferator-activated receptor (PPAR) signaling pathway, which were significantly enriched in the HF group compared with the low UFA group, were significantly and positively correlated with multiple UFA . The synthesis of UFA is mainly influenced by Bacteroides, Prevotella, and Bacteroidaceae, and regulated by fatty acid biosynthesis, fatty acid metabolism, and PPAR signaling pathways, which together influence the synthesis of UFA in buffaloes.
Collapse
Affiliation(s)
- Ye Yu
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Runqi Fu
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Chunjia Jin
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Huan Gao
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Lin Han
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Min Qi
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Binlong Fu
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Qian Li
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Yuyan Wang
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China
| | - Yanfen Cheng
- Laboratory of Gastrointestinal Microbiology, National Center for International Research on Animal Gut Nutrition, Nanjing Agricultural University, Nanjing 210095, China
| | - Jing Leng
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, China; Key Laboratory of Animal Nutrition and Feed Science of Yunnan Province, Yunnan Agricultural University, Kunming 650201, China.
| |
Collapse
|
12
|
Higuchi L, Ouchi N, Negishi Y, Naruo M, Kusano M, Suzuki S, Okuda T, Morita R. Ovariectomy-induced bone loss through inappropriate inflammatory response: an osteoimmunological perspective on postmenopausal osteoporosis. Immunol Med 2025:1-14. [PMID: 40377249 DOI: 10.1080/25785826.2025.2506870] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/26/2025] [Accepted: 05/12/2025] [Indexed: 05/18/2025] Open
Abstract
Postmenopausal osteoporosis (PO) is a prevalent condition that significantly impairs the quality of life in elderly women. While traditionally attributed to estrogen deficiency, emerging evidence suggests that immune dysregulation plays a critical role in its pathogenesis. This study investigates the osteoimmunological mechanisms underlying PO using an ovariectomy (Ovx) mouse model. Our findings indicate that Ovx mice exhibit substantial reductions in bone mineral density and bone volume, accompanied by a marked suppression of interleukin-4 (IL-4) and interferon-gamma (IFN-γ) production, particularly from natural killer T (NKT) cells. Lipidomic analysis of bone marrow further revealed an upregulation of omega-6 fatty acids, contributing to an inflammatory microenvironment that promotes excessive osteoclast activation. Notably, administration of the glycolipid OCH restored cytokine production and mitigated bone loss in Ovx mice, suggesting its therapeutic potential. These findings highlight the complex interplay between immune responses and lipid metabolism in PO and propose novel therapeutic strategies aimed at modulating immune function to prevent bone loss. This study offers valuable insights into the osteoimmunological mechanisms of PO and underscores the potential of immunomodulatory approaches for its management.
Collapse
Affiliation(s)
- Lilika Higuchi
- Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan
| | - Nozomi Ouchi
- Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan
| | - Yasuyuki Negishi
- Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan
- Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan
| | - Munehiro Naruo
- Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan
- Department of Orthopedic Surgery, Tomei Atsugi Hospital, Kanagawa, Japan
- Department of Orthopedic Surgery, Tokyo Women's Medical University, Tokyo, Japan
| | - Maiko Kusano
- Department of Legal Medicine, Showa University, Tokyo, Japan
| | - Shunji Suzuki
- Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan
| | - Takahisa Okuda
- Department of Legal Medicine, Nihon University School of Medicine, Tokyo, Japan
| | - Rimpei Morita
- Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan
| |
Collapse
|
13
|
Peng S, Zhu Y, Zhu J, Chen Z, Tao Y. Plasma-based untargeted metabolomics reveals potential biomarkers for screening and distinguishing of ovarian tumors. Clin Chim Acta 2025; 572:120246. [PMID: 40107594 DOI: 10.1016/j.cca.2025.120246] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/15/2024] [Revised: 03/05/2025] [Accepted: 03/15/2025] [Indexed: 03/22/2025]
Abstract
Ovarian cancer (OC), a leading cause of gynecological cancer mortality, is frequently detected at advanced stages due to asymptomatic early progression. This study investigates plasma-based untargeted metabolomics for identifying biomarkers to screen and differentiate ovarian tumors (OT). Plasma samples from OC, benign ovarian tumors (BOT), and healthy controls (HC) were analyzed. Samples were randomized into train and test sets, with differential metabolites screened via two-tailed Student's t-test and partial least squares discriminant analysis. ROC models evaluated discriminatory capacity. Key metabolites demonstrated high predictive value: TMAO and hippuric acid distinguished OT from HC (AUC > 0.95), while linoleic acid, alpha-linolenic acid, and arachidonic acid (AUC > 0.9) further supported OT screening. Kynurenine differentiated OC from BOT (AUC = 0.808). Reduced levels of specific lysophosphatidylcholines (LPC (17:0/0:0), LPC (15:0/0:0)) also distinguished OT from HC (AUC = 0.771-0.89). These findings suggest plasma metabolomics holds promise for noninvasive biomarker discovery in OT screening and distinguishing between malignant and benign cases, though further validation of metabolite quantification is warranted prior to clinical application.
Collapse
Affiliation(s)
- Shen Peng
- College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China
| | - Yiming Zhu
- Department of Gynecological Oncology, Zhejiang Cancer Hospital, Hangzhou, Zhejiang 310022, China
| | - Jing Zhu
- Department of Clinical Laboratory, Zhenjiang Cancer Hospital, Hangzhou, Zhejiang 310022, China
| | - Zhongjian Chen
- Experimental Research Center, Zhejiang Cancer Hospital, Hangzhou, Zhejiang 310022, China.
| | - Yi Tao
- College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, China.
| |
Collapse
|
14
|
Xiaona L, Lulu X, Han L, Pengyu Q, Huanhuan Z, Dandan L, Xiaobo W, Bingyan H, Maoning Z, Chenyu L, Zhongxin Z, Wenzhao D, Lei S, Xinyou Z. AhFAD3-A01 enhances α-linolenic acid content in Arabidopsis and peanut. Gene 2025; 949:149336. [PMID: 39986661 DOI: 10.1016/j.gene.2025.149336] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/07/2024] [Revised: 02/13/2025] [Accepted: 02/14/2025] [Indexed: 02/24/2025]
Abstract
Alpha-linolenic acid (ALA, C18:3) is an essential fatty acid integral to human growth and development. Despite its significance, the ALA content in peanut seeds-a major global oilseed crop-is notably low. This study employed bioinformatics analysis, tissue expression, and promoter function evaluations to investigate AhFAD3, which encodes the microsomal omega-3 fatty acid desaturase that is directly responsible for ALA accumulation through converting linoleic acid (LA) to ALA. We identified the active AhFAD3 gene, AhFAD3-A01, with the functional protein encoded by AhFAD3-A01 localized in the endoplasmic reticulum (ER) and found to be pivotal in ALA synthesis in seeds. The low expression of AhFAD3 genes during the late stages of seed development, coupled with the specific activation by only AhFAD3-A01 and AhFAD3-B01 promoters in seeds, results in the low ALA levels in mature peanut seeds. To enhance ALA content, the constitutive promoter CaMV35S and the seed-specific promoter PAhWRI1 were utilized to overexpress AhFAD3-A01 in Arabidopsis and peanut. While the expression level of AhFAD3-A01 in PAhWRI1::AhFAD3-A01 transgenic Arabidopsis remained unchanged, it significantly increased under the CaMV35S::AhFAD3-A01 configuration, leading to an over a 40 % increase in ALA content of in T4 generation seeds, indicating that PAhWRI1 was unable to drive AhFAD3 overexpression in Arabidopsis. Similarly, the overexpression of AhFAD3-A01 using both promoters in peanuts resulted in enhanced expression and an increase in ALA content from 15.18 % to 30.65 % in CaMV35S::AhFAD3-A01 T1 generation seeds and from 11.23 % to 25.49 % in PAhWRI1::AhFAD3-A01 seeds. These results highlight the critical role of AhFAD3-A01 ALA synthesis in peanut seeds and provide a solid foundation for developing peanut varieties with elevated ALA content.
Collapse
Affiliation(s)
- Li Xiaona
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Xue Lulu
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Liu Han
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Qu Pengyu
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Zhao Huanhuan
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Luo Dandan
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Wang Xiaobo
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Huang Bingyan
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Zhang Maoning
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Li Chenyu
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Zhang Zhongxin
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Dong Wenzhao
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China
| | - Shi Lei
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China.
| | - Zhang Xinyou
- Henan Academy of Crop Molecular Breeding, Henan, China; State Industrial Innovation Center of Biological Breeding, Henan, China; The Shennong Laboratory, Henan, China; Key Laboratory of Oil Crops in Huang-Huai-Hai Plains Ministry of Agriculture, Henan, China; Henan Provincial Key Laboratory for Oil Crops Improvement, Henan, China; Henan Academy of Agricultural Sciences, Graduate T & R Base of Zhengzhou University, Henan, China.
| |
Collapse
|
15
|
Tan X, Ni H, Li Q, Ma Z. Systematic Profile of Oxylipins in Myocardial Infarction by Liquid Chromatography-Tandem Mass Spectrometry. RAPID COMMUNICATIONS IN MASS SPECTROMETRY : RCM 2025; 39:e9999. [PMID: 39887460 DOI: 10.1002/rcm.9999] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Subscribe] [Scholar Register] [Received: 10/12/2024] [Revised: 01/18/2025] [Accepted: 01/20/2025] [Indexed: 02/01/2025]
Abstract
RATIONALE Oxylipins play an important role in inflammatory processes, accompanying the occurrence of myocardial infarction. Analyzing a wide panel of oxylipins derived from more polyunsaturated fatty acids may provide valuable information to elucidate the relationships between the signaling mediator profile and myocardial infarction comprehensively. METHODS An ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for simultaneously measuring 74 oxylipins in 50-μL human samples with a 10-min chromatographic run and easy operation has been developed and validated. RESULTS Accuracy and precision were below 15% of the relative errors in 99% of quality control. Recoveries and matrix effect were considered acceptable. Potential effects of different collecting tubes were also assessed. We successfully utilized our approach to measure plasma samples obtained from 99 healthy individuals and 302 myocardial infarction patients. CONCLUSIONS Profiles of oxylipins discovered potential biomarkers and clarified the pathological characteristics of oxylipin metabolism in myocardial infarction. Our approach was rapid, accurate, and precise, with high throughput, low sample volume, and easy operation, suitable for large-scale studies.
Collapse
Affiliation(s)
- Xin Tan
- Beijing Anzhen Hospital, Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing Collaborative Innovation Center for Cardiovascular Disorders, Capital Medical University, Beijing, China
- Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China
| | - Hui Ni
- Beijing Anzhen Hospital, Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing Collaborative Innovation Center for Cardiovascular Disorders, Capital Medical University, Beijing, China
- Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China
| | - Qin Li
- Beijing Anzhen Hospital, Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing Collaborative Innovation Center for Cardiovascular Disorders, Capital Medical University, Beijing, China
- Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China
| | - Zhanglin Ma
- Beijing Anzhen Hospital, Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing Collaborative Innovation Center for Cardiovascular Disorders, Capital Medical University, Beijing, China
- Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China
| |
Collapse
|
16
|
Wu J, Luo J, He Q, Zhang F, Shi C, Zhao J, Li C, Deng W. CD36 molecule and AMP-activated protein kinase signaling drive docosahexaenoic acid-induced lipid remodeling in goat mammary epithelial cells. Int J Biol Macromol 2025; 311:144076. [PMID: 40348225 DOI: 10.1016/j.ijbiomac.2025.144076] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/02/2025] [Revised: 04/28/2025] [Accepted: 05/07/2025] [Indexed: 05/14/2025]
Abstract
Goat milk is a vital component of China's dairy industry, renowned for its richness in lipids essential to human health. Polyunsaturated fatty acids (PUFAs), such as docosahexaenoic acid (C22:6n-3, DHA), are particularly valuable for their integration into phospholipids and triacylglycerols. While mammary cells can uptake and channel PUFAs into lipids for milk fat secretion, the broader functional effects of DHA within these cells remain unclear. This study demonstrated that DHA supplementation markedly altered levels of lipid subclasses in goat mammary epithelial cells (GMECs), as revealed by lipidomic analysis. DHA treatment significantly increased the levels of free DHA, alongside DHA-enriched triacylglycerols, phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine, thereby driving lipid remodeling in GMECs. Additionally, DHA modulated transcription of key fatty acid metabolism genes, such as SREBP1, FASD2, and FASN. Mechanistically, DHA supplementation activated the AMPK signaling pathway inhibiting fatty acid metabolism, and upregulated the expression of fatty acid transport gene-CD36 in GMECs. Knockdown or mutation of the fatty acid binding domain of CD36 diminished DHA-induced AMPK activation and transcriptional regulation of fatty acid metabolism genes in GMECs. In summary, DHA supplementation induces lipid remodeling in GMECs via the CD36-AMPK signaling axis, highlighting its potential to facilitate the development of DHA-enriched functional goat milk.
Collapse
Affiliation(s)
- Jiao Wu
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, People's Republic of China; College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Jun Luo
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China.
| | - Qiuya He
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Fuhong Zhang
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Chenbo Shi
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Jianqing Zhao
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Cong Li
- College of Animal Science and Technology, Northwest A & F University, Yangling 712100, People's Republic of China
| | - Weidong Deng
- Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming 650201, People's Republic of China
| |
Collapse
|
17
|
Qiao Y, Chen H, Guo J, Zhang X, Liang X, Wei L, Wang Q, Bi H, Gao T. A Study of Sex Differences in the Biological Pathways of Stress Regulation in Mice. CNS Neurosci Ther 2025; 31:e70433. [PMID: 40365748 PMCID: PMC12076126 DOI: 10.1111/cns.70433] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/26/2024] [Revised: 03/10/2025] [Accepted: 04/28/2025] [Indexed: 05/15/2025] Open
Abstract
BACKGROUND Stress is closely related to life, and it can also cause many mental disorders. However, there are significant sex differences in neuropsychiatric disorders associated with stress, particularly in depression, where the lifetime risk of depression in women is approximately twice that of men. However, the specific mechanism of this process has not been explained in detail. METHODS Chronic restraint stress (CRS) + chronic and unpredictable mild stress (CUMS) was used to simulate social stress, and behavioral experiments, HE staining of rectal and hippocampal pathological sections, detection of depression-related biological indicators, analysis of intestinal flora diversity, and metabolomics analysis of hippocampal and intestinal contents were performed. RESULTS The results showed that stress induced anxiety-like behavior in female mice and depression-like behavior in male mice. Sex differences in behavior may be related to monoamine neurotransmitters, hyperactivity of HPA axis, inflammatory factors, gut microbiota, and brain-gut metabolism. It is worth noting that stress caused opposite trends in DA (dopamine) levels, abundance of f-lactobaciliaceae, and levels of metabolites (1, 2-distearoyl-SN-glycero-3-phosphocholine) and PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:1(11Z)) in male and female mice. CONCLUSION The difference in neurotransmitter levels, the disorder of gut microbiota, and the abnormal brain and gut metabolism may lead to the gender difference in stress behavior.
Collapse
Affiliation(s)
- Yajun Qiao
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- School of PsychologyChengdu Medical CollegeChengduChina
- University of Chinese Academy of SciencesBeijingChina
| | - Hanxi Chen
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
| | - Juan Guo
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- School of PsychologyChengdu Medical CollegeChengduChina
| | - Xingfang Zhang
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- Medical College, Qinghai UniversityXiningChina
| | - Xinxin Liang
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- School of PsychologyChengdu Medical CollegeChengduChina
- University of Chinese Academy of SciencesBeijingChina
| | - Lixin Wei
- University of Chinese Academy of SciencesBeijingChina
- CAS Key Laboratory of Tibetan Medicine ResearchNorthwest Institute of Plateau Biology, Chinese Academy of SciencesXiningChina
| | - Qiannan Wang
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- School of PsychologyChengdu Medical CollegeChengduChina
| | - Hongtao Bi
- Qinghai Provincial Key Laboratory of Tibetan Medicine Pharmacology and Safety EvaluationNorthwest Institute of Plateau Biology, Chinese Academy of ScienceXiningChina
- University of Chinese Academy of SciencesBeijingChina
| | - Tingting Gao
- School of PsychologyChengdu Medical CollegeChengduChina
- Department of PsychiatryThe People's Hospital of Jiangmen, Southern Medical UniversityJiangmenChina
| |
Collapse
|
18
|
Kim JW, Tung HC, Yang B, Pant R, Guan X, Feng Y, Xie W. Heme-thiolate monooxygenase cytochrome P450 1B1, an old dog with many new tricks. Pharmacol Rev 2025; 77:100045. [PMID: 40054133 DOI: 10.1016/j.pharmr.2025.100045] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/15/2024] [Revised: 01/25/2025] [Accepted: 01/30/2025] [Indexed: 05/12/2025] Open
Abstract
Cytochrome P450 CYP1B1 is a heme-thiolate monooxygenase traditionally recognized for its xenobiotic functions and extrahepatic expressions. Recent studies have suggested that CYP1B1 is also expressed in hepatic stellate cells, immune cells, endothelial cells, and fibroblasts within the tumor microenvironment, as well as tumor cells themselves. CYP1B1 is responsible for the metabolism of a wide range of substrates, including xenobiotics such as drugs, environmental chemicals, and endobiotics such as steroids, retinol, and fatty acids. Consequently, CYP1B1 and its associated exogenous and endogenous metabolites have been critically implicated in the pathogenesis of many diseases. Understanding the mode of action of CYP1B1 in different pathophysiological conditions and developing pharmacological inhibitors that allow for systemic or cell type-specific modulation of CYP1B1 may pave the way for novel therapeutic opportunities. This review highlights the significant role of CYP1B1 in maintaining physiological homeostasis and provides a comprehensive discussion of recent advancements in our understanding of CYP1B1's involvement in the pathogenesis of diseases such as fibrosis, cancer, glaucoma, and metabolic disorders. Finally, the review emphasizes the therapeutic potential of targeting CYP1B1 for drug development, particularly in the treatment and prevention of cancers and liver fibrosis. SIGNIFICANCE STATEMENT: CYP1B1 plays a critical role in various physiological processes. Dysregulation or genetic mutations of the gene encoding this enzyme can lead to health complications and may increase the risk of diseases such as cancer and liver fibrosis. In this review, we summarize recent preclinical and clinical evidence that underscores the potential of CYP1B1 as a therapeutic target.
Collapse
Affiliation(s)
- Jong-Won Kim
- Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania
| | - Hung-Chun Tung
- Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania
| | - Bin Yang
- Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania
| | - Rajat Pant
- Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania
| | - Xiuchen Guan
- Department of Orthodontics, School of Stomatology, Capital Medical University, Beijing, China
| | - Ye Feng
- Department of Endocrinology and Metabolic Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
| | - Wen Xie
- Center for Pharmacogenetics, Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Pharmacology & Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
| |
Collapse
|
19
|
Sivri D, Akdevelioğlu Y. Effect of Fatty Acids on Glucose Metabolism and Type 2 Diabetes. Nutr Rev 2025; 83:897-907. [PMID: 39530757 PMCID: PMC11986341 DOI: 10.1093/nutrit/nuae165] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/16/2024] Open
Abstract
Type 2 diabetes is an inflammatory, non-infectious disease characterized by dysfunctional pancreatic β-cells and insulin resistance. Although lifestyle, genetic, and environmental factors are associated with a high risk of type 2 diabetes, nutrition remains one of the most significant factors. Specific types and increased amounts of dietary fatty acids are associated with type 2 diabetes and its complications. Dietary recommendations for the prevention of type 2 diabetes advocate for a diet that is characterized by reduced saturated fatty acids and trans fatty acids alongside an increased consumption of monounsaturated fatty acids, polyunsaturated fatty acids, and omega-3 fatty acids. Although following the recommendations for dietary fatty acid intake is important for reducing type 2 diabetes and its related complications, the underlying mechanisms remain unclear. This review will provide an update on the mechanisms of action of fatty acids on glucose metabolism and type 2 diabetes, as well as dietary recommendations for the prevention of type 2 diabetes.
Collapse
Affiliation(s)
- Dilek Sivri
- Department of Nutrition and Dietetics, Faculty of Health Science, Anadolu University, Eskişehir, Türkiye
| | - Yasemin Akdevelioğlu
- Department of Nutrition and Dietetics, Faculty of Health Science, Gazi University, Ankara, Türkiye
| |
Collapse
|
20
|
Chen M, Lu S, Qi Y, Zheng N, Li L, Huang L, Zhao Y, Meng L, Zhang Y, Wang J. Fatty acidomics unveils seasonal variations in nutritional quality of buffalo and camel milk. J Dairy Sci 2025:S0022-0302(25)00280-2. [PMID: 40306428 DOI: 10.3168/jds.2024-26204] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/20/2024] [Accepted: 04/01/2025] [Indexed: 05/02/2025]
Abstract
Interest in nonbovine milk, such as buffalo and camel milk, for human consumption is increasing, yet information on their nutritional quality is limited. This study aimed to investigate the fatty acid profiles of camel and buffalo milk, focusing on how species and seasonal variations affect their nutritional value. Buffalo milk and camel milk samples were collected respectively from the Guangxi Zhuang Autonomous Region and Xinjiang Uyghur Autonomous Region of China over the year. A total of 88 fatty acids (C1-C24) were quantified using GC-MS as part of a comprehensive fatty acidomics approach. The results showed that species differences had a greater impact on fatty acid profiles than seasonal variations. Buffalo milk had higher concentrations of short-chain fatty acids, especially C4:0, whereas camel milk was richer in UFA. In autumn and winter, both milks had higher levels of even-chain SFA and UFA (n-1, n-3, n-5, n-6, n-7, n-12). Conversely, milk in spring and summer had higher levels of n-9 UFA, even- and branch-chain SFA. Camel milk showed more favorable fatty acid characteristics, including an optimal n-6/n-3 PUFA ratio for reducing inflammation and cardiovascular risks. In autumn, both milks had higher n-6/n-3 PUFA ratios, PUFA/SFA ratios, and health promoting index, and lower atherogenic index, thrombogenic index, and hypocholesterolemic/hypercholesterolemic ratios. These findings highlight the potential for developing species-specific dairy products and offer insights for optimizing milk quality through seasonal adjustments in feeding and management.
Collapse
Affiliation(s)
- Meiqing Chen
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Songcui Lu
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Yingjie Qi
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Nan Zheng
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Ling Li
- Guangxi Zhuang Autonomous Region Buffalo Milk Quality and Safety Control Technology Engineering Research Center, Guangxi Buffalo Research Institute, Chinese Academy of Agricultural Sciences, 530001 Nanning, China
| | - Li Huang
- Guangxi Zhuang Autonomous Region Buffalo Milk Quality and Safety Control Technology Engineering Research Center, Guangxi Buffalo Research Institute, Chinese Academy of Agricultural Sciences, 530001 Nanning, China
| | - Yankun Zhao
- Institute of Quality Standards & Testing Technology for Agro-products, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, China
| | - Lu Meng
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Yangdong Zhang
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China
| | - Jiaqi Wang
- Key Laboratory of Quality & Safety Control for Milk and Dairy Products of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China; Milk and Milk Products Inspection Center of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China.
| |
Collapse
|
21
|
Geertsema J, Juncker HG, Wilmes L, Burchell GL, de Rooij SR, van Goudoever JB, O'Riordan KJ, Clarke G, Cryan JF, Korosi A. Nutritional interventions to counteract the detrimental consequences of early-life stress. Mol Psychiatry 2025:10.1038/s41380-025-03020-1. [PMID: 40289212 DOI: 10.1038/s41380-025-03020-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 04/19/2024] [Revised: 03/19/2025] [Accepted: 04/07/2025] [Indexed: 04/30/2025]
Abstract
Exposure to stress during sensitive developmental periods comes with long term consequences for neurobehavioral outcomes and increases vulnerability to psychopathology later in life. While we have advanced our understanding of the mechanisms underlying the programming effects of early-life stress (ES), these are not yet fully understood and often hard to target, making the development of effective interventions challenging. In recent years, we and others have suggested that nutrition might be instrumental in modulating and possibly combatting the ES-induced increased risk to psychopathologies and neurobehavioral impairments. Nutritional strategies are very promising as they might be relatively safe, cheap and easy to implement. Here, we set out to comprehensively review the existing literature on nutritional interventions aimed at counteracting the effects of ES on neurobehavioral outcomes in preclinical and clinical settings. We identified eighty six rodent and ten human studies investigating a nutritional intervention to ameliorate ES-induced impairments. The human evidence to date, is too few and heterogeneous in terms of interventions, thus not allowing hard conclusions, however the preclinical studies, despite their heterogeneity in terms of designs, interventions used, and outcomes measured, showed nutritional interventions to be promising in combatting ES-induced impairments. Furthermore, we discuss the possible mechanisms involved in the beneficial effects of nutrition on the brain after ES, including neuroinflammation, oxidative stress, hypothalamus-pituitary-adrenal axis regulation and the microbiome-gut-brain axis. Lastly, we highlight the critical gaps in our current knowledge and make recommendations for future research to move the field forward.
Collapse
Affiliation(s)
- Jorine Geertsema
- Brain Plasticity group, Centre for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands
| | - Hannah G Juncker
- Brain Plasticity group, Centre for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands
- Amsterdam UMC, University of Amsterdam, Vrije Universiteit, Emma Children's Hospital, Amsterdam, The Netherlands
- Amsterdam Reproduction and Development, Amsterdam, The Netherlands
| | - Lars Wilmes
- APC Microbiome Ireland, University College Cork, Cork, Ireland
- Department of Anatomy and Neuroscience, University College Cork, Cork, Ireland
- Department of Psychiatry and Neurobehavioural Science, University College Cork, Cork, Ireland
| | - George L Burchell
- Medical Library, Vrije Universiteit Amsterdam, Amsterdam, Netherlands
| | - Susanne R de Rooij
- Amsterdam Reproduction and Development, Amsterdam, The Netherlands
- Amsterdam UMC location University of Amsterdam, Department of Epidemiology and Data Science, Meibergdreef 9, Amsterdam, The Netherlands
- Amsterdam Public Health research institute, Aging and Later Life, Health Behaviors and Chronic Diseases, Amsterdam, The Netherlands
| | - J B van Goudoever
- Amsterdam UMC, University of Amsterdam, Vrije Universiteit, Emma Children's Hospital, Amsterdam, The Netherlands
- Amsterdam Reproduction and Development, Amsterdam, The Netherlands
| | | | - Gerard Clarke
- APC Microbiome Ireland, University College Cork, Cork, Ireland
- Department of Psychiatry and Neurobehavioural Science, University College Cork, Cork, Ireland
| | - John F Cryan
- APC Microbiome Ireland, University College Cork, Cork, Ireland
- Department of Anatomy and Neuroscience, University College Cork, Cork, Ireland
- Department of Psychiatry and Neurobehavioural Science, University College Cork, Cork, Ireland
| | - Aniko Korosi
- Brain Plasticity group, Centre for Neuroscience, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
| |
Collapse
|
22
|
Chon JE, Semnani-Azad Z, Lai KZH, Connelly PW, Retnakaran R, Harris SB, Metherel AH, Jenkins DJA, Bazinet RP, Hanley AJ. Omega-3 Polyunsaturated Fatty Acids And Adipose Tissue Inflammation: Longitudinal Analysis in the PROMISE Cohort. J Clin Endocrinol Metab 2025; 110:1324-1333. [PMID: 38943663 PMCID: PMC12012786 DOI: 10.1210/clinem/dgae445] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 12/12/2023] [Revised: 06/17/2024] [Accepted: 06/27/2024] [Indexed: 07/01/2024]
Abstract
OBJECTIVES Although preclinical studies have shown a beneficial impact of omega-3 (n-3) polyunsaturated fatty acids (PUFAs) on adipose tissue (AT) inflammation, the current literature from human studies is limited. Therefore, we aimed to evaluate the longitudinal associations of circulating levels of n-3 PUFAs with biomarkers of AT inflammation. METHODS Longitudinal data from participants in the PROMISE cohort (n = 474) were used. AT inflammation was measured using circulating biomarkers at baseline and up to 2 follow-up visits. n-3 PUFAs were measured at baseline in 4 serum lipid fractions. Generalized estimating equations analyses evaluated longitudinal associations between n-3 PUFAs and AT inflammation, adjusting for covariates. RESULTS Fully adjusted generalized estimating equation models indicated that higher baseline proportions of eicosapentaenoic acid, n-3 docosapentaenoic acid, and docosahexaenoic acid in total serum were significantly inversely associated with longitudinal change in soluble CD163 (all P < .05). A significant positive association of n-3 docosapentaenoic acid and docosahexaenoic acid with longitudinal change in adiponectin (P < .05) was also observed. Generally consistent associations were observed between n-3 PUFAs and soluble CD163 and adiponectin in the four lipid fractions. CONCLUSION These findings will add to the limited evidence on the potential role n-3 PUFAs have in the prevention and management of AT inflammation in humans and may help inform future interventions targeting chronic inflammation at the level of AT.
Collapse
Affiliation(s)
- Ji-Eun Chon
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
| | - Zhila Semnani-Azad
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
- Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA
| | - Kira Zhi Hua Lai
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
| | - Phillip W Connelly
- Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, ON M5B 1M4, Canada
- Division of Endocrinology and Metabolism, University of Toronto, Toronto, ON M5S 3H2, Canada
- Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5S 1A8, Canada
| | - Ravi Retnakaran
- Division of Endocrinology and Metabolism, University of Toronto, Toronto, ON M5S 3H2, Canada
- Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada
- Leadership Sinai Centre for Diabetes, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada
| | - Stewart B Harris
- Department of Family Medicine, Western University, London, ON N6G 2M1, Canada
| | - Adam H Metherel
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
| | - David J A Jenkins
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
- Toronto 3D Knowledge Synthesis and Clinical Trials Unit, Clinical Nutrition and Risk Factor Modification Center, St. Michael's Hospital, Toronto, ON M5C 2T2, Canada
- Clinical Nutrition and Risk Factor Modification Centre, St. Michael's Hospital, Toronto, ON M5B 1W8, Canada
- Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
- Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, ON M5B 1W8, Canada
- Division of Endocrinology and Metabolism, St. Michael's Hospital, Toronto, ON M5B 1W8, Canada
| | - Richard P Bazinet
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
| | - Anthony J Hanley
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada
- Division of Endocrinology and Metabolism, University of Toronto, Toronto, ON M5S 3H2, Canada
- Leadership Sinai Centre for Diabetes, Mount Sinai Hospital, Toronto, ON M5G 1X5, Canada
- Dalla Lana School of Public Health, University of Toronto, Toronto, ON M5T 3M7, Canada
| |
Collapse
|
23
|
Ferreira YAM, Estadella D, Pisani LP. Effect of Different Fatty Acid Types on Mitochondrial Dysfunction Associated With Brown and Beige Adipose Tissue. Nutr Rev 2025:nuaf048. [PMID: 40233210 DOI: 10.1093/nutrit/nuaf048] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/17/2025] Open
Abstract
Adipose tissue serves as a dynamic endocrine organ that is pivotal in metabolic regulation. Augmenting mitochondrial activity within this tissue holds promise in combating obesity. Mitochondrial function is intricately modulated by diverse fatty acid compositions. This comprehensive review aimed to elucidate the molecular mechanisms underlying mitochondrial dysfunction induced by various fatty acid profiles. While saturated fatty acids (SFAs) pose a threat to mitochondrial integrity, polyunsaturated fatty acids (PUFAs), notably n-3, mitigate SFA-induced damage, concurrently regulating thermogenic gene expression. With regard to monounsaturated fatty acids (MUFAs), their impact on mitochondrial function in adipose tissue remains relatively unexplored. Although human studies are imperative for comprehensive insights, prioritizing the consumption of n-3 fatty acids and MUFAs has emerged as a strategic approach, potentially enhancing mitochondrial biogenesis and metabolic pathways. This synthesis underscores the critical need for further investigation of the differential effects of fatty acid types on adipose tissue mitochondria, offering potential avenues for obesity intervention.
Collapse
Affiliation(s)
- Yasmin Alaby Martins Ferreira
- Department of Biosciences, Institute of Health and Science, Federal University of São Paulo (UNIFESP), Santos, SP 11015-020, Brazil
| | - Débora Estadella
- Department of Biosciences, Institute of Health and Science, Federal University of São Paulo (UNIFESP), Santos, SP 11015-020, Brazil
| | - Luciana Pellegrini Pisani
- Department of Biosciences, Institute of Health and Science, Federal University of São Paulo (UNIFESP), Santos, SP 11015-020, Brazil
| |
Collapse
|
24
|
Klein L, Lenz C, Krüger K, Lorkowski S, Kipp K, Dawczynski C. Comparative analysis of fatty acid profiles across omnivorous, flexitarians, vegetarians, and vegans: insights from the NuEva study. Lipids Health Dis 2025; 24:133. [PMID: 40205391 PMCID: PMC11983864 DOI: 10.1186/s12944-025-02517-6] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/22/2024] [Accepted: 03/09/2025] [Indexed: 04/11/2025] Open
Abstract
BACKGROUND Different dietary choices can influence blood fatty acid profiles, which are crucial for maintaining physiological health and reducing disease risk. In particular, the exclusion of animal foods in vegetarian diets is associated with a higher risk of undersupply of long-chain omega (n)-3 fatty acids, which could, potentially, have a negative effect on inflammation. This study aimed to examine differences in plasma and erythrocyte fatty acid profiles as well as inflammation-related biomarkers between various plant-based diets and a regular omnivores diet. METHODS The Nutritional Evaluation (NuEva) study is a is a parallel-designed trial. Here screening data was used to investigate differences in plasma and erythrocyte fatty acid profiles across omnivores (Western diet; n = 62), flexitarians (n = 69), vegetarians (n = 64) and vegans (n = 57). Furthermore, markers associated with inflammation are investigated and correlated with selected fatty acids. RESULTS Flexitarians showed lower erythrocyte saturated fatty acids (SFA) than omnivores, while vegans had the lowest plasma SFA. Vegans had higher erythrocyte monounsaturated fatty acids proportions, like oleic acid, than flexitarians and vegetarians. n-6 fatty acids, particularly linoleic acid, were highest in vegans and vegetarians. Conversely, omnivores had higher arachidonic acid in erythrocytes. Vegans had lower n-3 fatty acids in both plasma and erythrocytes, also reflected in a lower n-3 index (eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA)) values, indicating a trend with restriction of animal foods: omnivores/flexitarians > vegetarians > vegans. While interleukin (IL)-6, IL-8, IL-10, tumor necrosis factor (TNF)-α and high-sensitive C-reactive protein (hsCRP) did not differ between groups, and vegans had lower leptin levels compared to omnivores. CONCLUSIONS The NuEva study revealed significant impact of dietary patterns on fatty acid profiles, with vegans and vegetarians displaying lower concentrations of SFA and n-3 fatty acids, including EPA and DHA, compared to omnivores and flexitarians. Despite the clear differences in fatty acid profiles across the diets, the inflammatory markers measured in our healthy collective are comparable. TRIAL REGISTRATION Registered under ClinicalTrials.gov Identifier no. NCT03582020.
Collapse
Affiliation(s)
- Lea Klein
- Junior Research Group Nutritional Concepts, Institute of Nutritional Sciences, Friedrich Schiller University Jena, 07743, Jena, Germany
| | - Claudia Lenz
- Institute for Sports Science, Department of Exercise Physiology and Sports Therapy, University of Giessen, 35394, Giessen, Germany
| | - Karsten Krüger
- Institute for Sports Science, Department of Exercise Physiology and Sports Therapy, University of Giessen, 35394, Giessen, Germany
| | - Stefan Lorkowski
- Competence Cluster for Nutrition and Cardiovascular Health (nutriCARD) Halle-Jena-Leipzig, 07743, Jena, Germany
- Institute of Nutritional Sciences, Friedrich Schiller University Jena, 07743, Jena, Germany
| | - Kristin Kipp
- Department for Pediatrics, University Hospital Jena, Jena, Germany
| | - Christine Dawczynski
- Junior Research Group Nutritional Concepts, Institute of Nutritional Sciences, Friedrich Schiller University Jena, 07743, Jena, Germany.
- Competence Cluster for Nutrition and Cardiovascular Health (nutriCARD) Halle-Jena-Leipzig, 07743, Jena, Germany.
| |
Collapse
|
25
|
Assefa M, Zhao Y, Zhou C, Song Y, Zhao X. Advancements in Crop PUFAs Biosynthesis and Genetic Engineering: A Systematic and Mixed Review System. Int J Mol Sci 2025; 26:3462. [PMID: 40331974 PMCID: PMC12027219 DOI: 10.3390/ijms26083462] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/24/2025] [Revised: 03/24/2025] [Accepted: 03/31/2025] [Indexed: 05/08/2025] Open
Abstract
Recent advances in molecular studies on plant lipids have revealed novel functions, increasing interest in their roles in plant metabolic processes and food functionality. With evolving living standards, the demand for crop-derived polyunsaturated fatty acids (PUFAs) oil is increasing due to their benefits for cardiovascular health, brain function, and anti-inflammatory properties. Despite these benefits, there are gaps in comprehensive, integrated, and consolidated documents on recent advancements in crop biotechlogy, particularly concerning the biosynthesis of essential lipids. Such a document could provide valuable insights for researchers, breeders, and industry professionals seeking to enhance crop oil profiles and optimize the nutritional and functional qualities of plant-based foods. Therefore, this study aims to: (1) provide an updated review of crop lipid biosynthesis and (2) identify trending topics, key contributors, and institutions contributing to research on crop PUFAs, their health benefits, and genes associated with these functions. Methods: Systematic and mixed-method review approaches were used to gather the most recent evidence by identifying all relevant primary research studies on the specific review topic. Five databases were used in the process. Result and conclusion: 366 papers were identified, with 73 highly cited and recent ones focusing on crop PUFA biosynthesis and genetic engineering. Key genes involved in lipid biosynthesis include FAD, TMT, HGG, GhKAR, GhHAD, and transcription factors like MYB89, MYB96, WRI, LEC, GL2, FUS3, and HB2 all critical for enhancing PUFA biosynthesis. However, challenges such as poor transgene expression, reduced seed germination, and metabolic toxicity must be addressed to develop crops with improved oil profiles.
Collapse
Affiliation(s)
- Molalign Assefa
- Colin Ratledge Center for Microbial Lipids, School of Agricultural Engineering and Food Science, Shandong University of Technology, Zibo 255000, China;
- State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian 271018, China; (Y.Z.); (C.Z.)
| | - Yajie Zhao
- State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian 271018, China; (Y.Z.); (C.Z.)
| | - Chao Zhou
- State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian 271018, China; (Y.Z.); (C.Z.)
| | - Yuanda Song
- Colin Ratledge Center for Microbial Lipids, School of Agricultural Engineering and Food Science, Shandong University of Technology, Zibo 255000, China;
| | - Xiangyu Zhao
- State Key Laboratory of Crop Biology, College of Life Sciences, Shandong Agricultural University, Taian 271018, China; (Y.Z.); (C.Z.)
| |
Collapse
|
26
|
Harisha CB, Boraiah KM, Basavaraj PS, Halli HM, Singh RN, Rane J, Sammi Reddy K, Halagundegowda GR, Chaudhary A, Verma AK, Ravi Y, Asangi H, Senthamil E. Optimizing sowing time and weather conditions for enhanced growth and seed yield of chia ( Salvia hispanica L.) in semi-arid regions. PeerJ 2025; 13:e19210. [PMID: 40226547 PMCID: PMC11988109 DOI: 10.7717/peerj.19210] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/15/2024] [Accepted: 03/05/2025] [Indexed: 04/15/2025] Open
Abstract
Background Climate influenced weather events, especially during the flowering, grain filling, and maturity stages, can adversely influence crop yield and quality. Therefore, understanding how the phenological behaviour and yield potential of new crops such as chia are influenced by weather and sowing dates is crucial for maximizing crop yield. This study aimed to assess the impact of sowing dates on the flowering behaviour, and yield attributes of chia morphotypes, as well as to identify optimal weather conditions for achieving higher yields. Methods The study was conducted during 2021-22 and 2022-23 and consisted of fifteen sowing windows from 1st July to 1st February (at 15 days intervals), with two chia morphotypes (white and black seed) arranged in a replicated split-plot design. Phenological events, flowering characters and seed yield traits were recorded regularly. Weather parameters at the experimental location (Maharashtra, India) were recorded. Results The results revealed that weather conditions such as relative humidity (RH) and rainfall favoured the flowering phenology, yield attributes, and seed yield of chia, whereas maximum temperature (Tmax), bright sunshine hours, and accumulated growing degree days had negative effects. Weather parameters significantly influenced the chia seed yield during the cropping period: RH (positive, R 2 = 86.1%), Tmax (negative, R 2 = 67.4%), rainfall (positive, R 2 = 52.9%), and diurnal temperature range (negative, R 2 = 74.9%). Black-seeded chia morphotypes consistently produced higher seed yields (10.8% greater) and better yield-contributing traits compared to white types across various sowing dates. The maximum chia seed yield (811-793.1 kg ha-1) was achieved with sowing dates between August 1st and September 1st in this semi-arid region of India. The performance of chia was good under congenial weather conditions, including relative humidity (∼67-72%), maximum temperature (∼30-31 °C), day length (<12.0 h), rainfall (∼200-350 mm), and accumulated growing degree days (∼1,521-1,891). The present study findings can help identify the best suitable regions for chia cultivation by revealing relationships between the performance of chia morphotypes and weather conditions.
Collapse
Affiliation(s)
- CB Harisha
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | - KM Boraiah
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | - PS Basavaraj
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | - Hanamant M. Halli
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | - Ram Narayan Singh
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | - Jagadish Rane
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
- ICAR-Central Institute of Arid Horticulture, Bikaner, Rajasthan, India
| | - K Sammi Reddy
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
| | | | - Amresh Chaudhary
- ICAR-National Institute of Abiotic Stress Management, Baramati, Maharashtra, India
- ICAR-Central Soil Salinity Research Institute, Karnal, Haryana, India
| | | | - Y Ravi
- ICAR-National Research Centre on Seed Spices, Ajmer, Rajasthan, India
| | - Honnappa Asangi
- ICAR-Indian Institute of Spice Research Regional Station, Appangala, Karnataka, India
| | - E Senthamil
- University of Agricultural Sciences, Dharwad, Karnataka, India
| |
Collapse
|
27
|
Suzuki T, Yoshizawa Y, Takano S. Extent of Unidentified Complaints and Depression Is Inversely Associated with Fish and Shellfish Intake in Young Japanese Women. Nutrients 2025; 17:1252. [PMID: 40219009 PMCID: PMC11990306 DOI: 10.3390/nu17071252] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/11/2025] [Revised: 03/28/2025] [Accepted: 03/31/2025] [Indexed: 04/14/2025] Open
Abstract
Background/Objectives: Vague physical complaints with no corresponding organic disease background are called unidentified complaints. The symptoms of patients with unidentified complaints closely resemble medically unexplained or persistent physical symptoms, with the onset sometimes masked by mental disorders. Over the past 50 years, numerous studies have connected unfavorable eating habits to these symptoms; however, no study has systematically examined the association between the symptoms and specific nutrients or food items. Methods: We conducted a cross-sectional study of young Japanese women, using questionnaire surveys, to assess their nutritional intake, quantify unidentified complaints and depression, and identify nutrients/food items primarily associated with the severity of these conditions. Results: Our findings indicate that participants with high scores for unidentified complaints, depression, or both had lower intake levels of eicosapentaenoic acid, docosahexaenoic acid, vitamin D, and vitamin B12 than those with low scores, alongside reduced fish and shellfish consumption. Notably, the median fish and shellfish intake in the group with high scores for both unidentified complaints and depression was less than one-fourth of that in the low-score group. Conclusions: The results align with previous findings, demonstrating a modest inverse association between fish intake and depression risk, and suggesting the involvement of fish and shellfish intake in the occurrence of unidentified complaints.
Collapse
Affiliation(s)
- Toshikazu Suzuki
- Graduate School of Human Ecology, Wayo Women’s University, 2-3-1 Konodai, Ichikawa, Chiba 272-8533, Japan
- Department of Health and Nutrition, Wayo Women’s University, 2-3-1 Konodai, Ichikawa, Chiba 272-8533, Japan; (Y.Y.); (S.T.)
| | - Yui Yoshizawa
- Department of Health and Nutrition, Wayo Women’s University, 2-3-1 Konodai, Ichikawa, Chiba 272-8533, Japan; (Y.Y.); (S.T.)
| | - Shiori Takano
- Department of Health and Nutrition, Wayo Women’s University, 2-3-1 Konodai, Ichikawa, Chiba 272-8533, Japan; (Y.Y.); (S.T.)
| |
Collapse
|
28
|
Laureano G, Matos AR, Figueiredo A. Exploring the potential of lipid elicitors to enhance plant immunity. Prog Lipid Res 2025; 98:101332. [PMID: 40139324 DOI: 10.1016/j.plipres.2025.101332] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/26/2024] [Revised: 02/07/2025] [Accepted: 03/21/2025] [Indexed: 03/29/2025]
Abstract
Lipids besides being components of membranes and storage molecules are also involved in signalling processes and have proven to be vital components in plant defence mechanisms. Over the past decades, the intricate lipid-signalling pathways that underlie the establishment of defence responses have been extensively studied. These molecules can act directly as signalling agents in plant defence or serve as precursors in a plethora of biosynthetic pathways, leading to the production of phytohormones and other signalling agents. Lipids have proven to be promising elicitors by not only trigger a robust and appropriate defence response, across various plant species, but also induce resistance against a wide range of pathogens. Allied to this, lipids are widespread molecules in nature, which makes them an accessible resource and highlights their potential use as a sustainable approach to crop protection. This comprehensive review emphasizes the potential of lipids and lipid-derived molecules as elicitors in developing sustainable agricultural practices. By leveraging the natural defence mechanisms of plants, lipid elicitors offer a viable and eco-friendly alternative to conventional pest management strategies, contributing to the overall goal of sustainable agriculture.
Collapse
Affiliation(s)
- Gonçalo Laureano
- Grapevine Pathogen Systems lab, BioISI, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal; BioISI-Biosystems & Integrative Sciences Institute, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal.
| | - Ana Rita Matos
- BioISI-Biosystems & Integrative Sciences Institute, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal; Departamento de Biologia Vegetal, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal
| | - Andreia Figueiredo
- Grapevine Pathogen Systems lab, BioISI, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal; BioISI-Biosystems & Integrative Sciences Institute, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal; Departamento de Biologia Vegetal, Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisbon, Portugal
| |
Collapse
|
29
|
Altendorfer B, Benedetti A, Mrowetz H, Bernegger S, Bretl A, Preishuber-Pflügl J, Bessa de Sousa DM, Ladek AM, Koller A, Le Faouder P, Bertrand-Michel J, Trost A, Aigner L. Omega-3 EPA Supplementation Shapes the Gut Microbiota Composition and Reduces Major Histocompatibility Complex Class II in Aged Wild-Type and APP/PS1 Alzheimer's Mice: A Pilot Experimental Study. Nutrients 2025; 17:1108. [PMID: 40218866 PMCID: PMC11990804 DOI: 10.3390/nu17071108] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/28/2025] [Revised: 03/14/2025] [Accepted: 03/20/2025] [Indexed: 04/14/2025] Open
Abstract
Background/Objectives: Neuroinflammation, a hallmark of Alzheimer's disease (AD), is characterized by elevated levels of inflammatory signaling molecules, including cytokines and eicosanoids, as well as increased microglial reactivity, and is augmented by gut microbiota dysbiosis via the gut-brain axis. We conducted a pilot experiment to elucidate the anti-inflammatory effects of dietary omega-3 polyunsaturated fatty acid (ω-3 PUFA) eicosapentaenoic acid (EPA) on the gut microbiota and neuroinflammation. Methods: Female APP/PS1 mice (TG) and non-transgenic littermates (WT), 13-14 months old, were fed a diet supplemented with 0.3% EPA or control chow for 3 weeks. The gut microbiota composition, hippocampal and plasma eicosanoids levels, platelet activation, and microglial phagocytosis, as well as the brain and retinal genes and protein expression, were analyzed. Results: EPA supplementation decreased the percentage of Bacteroidetes and increased bacteria of the phylum Firmicutes in APP/PS1 and WT mice. Inflammatory lipid mediators were elevated in the hippocampus of the TG mice, accompanied by a reduction in the endocannabinoid docosahexaenoyl ethanolamide (DHEA). Dietary EPA did not affect hippocampal lipid mediators, but reduced the levels of arachidonic-derived 5-HETE and N-arachidonoylethanolamine (AEA) in WT plasma. Moreover, EPA supplementation decreased major histocompatibility complex class II (MHCII) gene expression in the retina in both genotypes, and MHCII+ cells in the hippocampus of TG mice. Conclusions: This pilot study showed that short-term EPA supplementation shaped the gut microbiota by increasing butyrate-producing bacteria of the Firmicutes phylum and decreasing Gram-negative LPS-producing bacteria of the Bacteroidetes phylum, and downregulated the inflammatory microglial marker MHCII in two distinct regions of the central nervous system (CNS). Further investigation is needed to determine whether EPA-mediated effects on the microbiome and microglial MHCII have beneficial long-term effects on AD pathology and cognition.
Collapse
Affiliation(s)
- Barbara Altendorfer
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
| | - Ariane Benedetti
- Institute of Experimental Neuroregeneration, Paracelsus Medical University, 5020 Salzburg, Austria;
| | - Heike Mrowetz
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
| | - Sabine Bernegger
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
| | - Alina Bretl
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
| | - Julia Preishuber-Pflügl
- Research Program for Experimental Ophthalmology and Glaucoma Research, Department of Ophthalmology and Optometry, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria; (J.P.-P.); (A.M.L.); (A.K.); (A.T.)
| | - Diana Marisa Bessa de Sousa
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
| | - Anja Maria Ladek
- Research Program for Experimental Ophthalmology and Glaucoma Research, Department of Ophthalmology and Optometry, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria; (J.P.-P.); (A.M.L.); (A.K.); (A.T.)
| | - Andreas Koller
- Research Program for Experimental Ophthalmology and Glaucoma Research, Department of Ophthalmology and Optometry, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria; (J.P.-P.); (A.M.L.); (A.K.); (A.T.)
| | - Pauline Le Faouder
- MetaToul-Lipidomique Core Facility, I2MC, Inserm 1048, 31432 Toulouse, France; (P.L.F.); (J.B.-M.)
| | - Justine Bertrand-Michel
- MetaToul-Lipidomique Core Facility, I2MC, Inserm 1048, 31432 Toulouse, France; (P.L.F.); (J.B.-M.)
| | - Andrea Trost
- Research Program for Experimental Ophthalmology and Glaucoma Research, Department of Ophthalmology and Optometry, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria; (J.P.-P.); (A.M.L.); (A.K.); (A.T.)
| | - Ludwig Aigner
- Institute of Molecular Regenerative Medicine, Paracelsus Medical University, 5020 Salzburg, Austria; (B.A.); (H.M.); (S.B.); (A.B.); (D.M.B.d.S.)
- Austrian Cluster of Tissue Regeneration, 1200 Vienna, Austria
| |
Collapse
|
30
|
Tian A, Xu L, Szeto IMY, Wang X, Li D. Effects of Different Proportions of DHA and ARA on Cognitive Development in Infants: A Meta-Analysis. Nutrients 2025; 17:1091. [PMID: 40292560 PMCID: PMC11946645 DOI: 10.3390/nu17061091] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/16/2025] [Revised: 03/10/2025] [Accepted: 03/14/2025] [Indexed: 04/30/2025] Open
Abstract
OBJECTIVES Previous studies have assessed the effect of docosahexaenoic acid (DHA, 22:6n-3) and arachidonic acid (ARA, 20:4n-6)-supplemented infant formula on brain development and cognitive function in infants. However, the results have been inconsistent. The aim of this systematic review and meta-analysis was to assess the effect of DHA and ARA supplementation on cognitive function in infants from randomized controlled trials (RCTs). METHODS We systematically searched and identified relevant literature from the PubMed, Web of Science, and Embase databases up to July 2024. Standard methods were applied to assess publication bias, sensitivity analysis, and heterogeneity among the included studies. A total of nine RCTs were included in the study, which comprised 1039 subjects. RESULTS Meta-analysis showed significantly positive effects of DHA and ARA supplementation on cognitive development in infants (Standardized Mean Difference (SMD): 0.21; 95% CI: 0.03, 0.38). No significant difference was found in Mental Development Index (MDI) score (Weighted Mean Difference (WMD): 0.20; 95% CI: -0.03, 0.43) and Psychomotor Development Index (PDI) score (WMD: 0.12; 95% CI: -0.11, 0.35) in Bayley Scales of Infant and Toddler Development compared with the control group. In subgroup analysis, when DHA/ARA was 0.5-1, PDI had a significant difference (WMD: 0.48; 95% CI: 0.03, 0.93) compared with the control group, with no significant difference between heterogeneity (I2 = 46.4%, p = 0.155). In comparison to the control group, significant differences were observed in MDI when DHA/ARA levels were between 0.5 and 1 (WMD: 0.55; 95% CI: 0.07, 1.02), with no significant difference between heterogeneity (I2 = 51.6%, p = 0.127). CONCLUSION When the DHA /ARA was 0.5-1 can significantly improve the cognitive function in infants.
Collapse
Affiliation(s)
- Ailing Tian
- Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao 266071, China; (A.T.); (L.X.)
| | - Lirong Xu
- Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao 266071, China; (A.T.); (L.X.)
| | - Ignatius Man-Yau Szeto
- National Center of Technology Innovation for Dairy, Hohhot 010110, China; (I.M.-Y.S.); (X.W.)
| | - Xuemin Wang
- National Center of Technology Innovation for Dairy, Hohhot 010110, China; (I.M.-Y.S.); (X.W.)
| | - Duo Li
- Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao 266071, China; (A.T.); (L.X.)
| |
Collapse
|
31
|
Yu J, Naseem S, Park S, Hur S, Choi Y, Lee T, Li X, Choi S. FASN, SCD, and PLAG1 Gene Polymorphism and Association with Carcass Traits and Fatty Acid Profile in Hanwoo Cattle. Animals (Basel) 2025; 15:897. [PMID: 40150426 PMCID: PMC11939486 DOI: 10.3390/ani15060897] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/27/2025] [Revised: 03/18/2025] [Accepted: 03/19/2025] [Indexed: 03/29/2025] Open
Abstract
Genetic polymorphisms have a great impact on enhancing quantitative traits in cattle. In this study, Fatty acid synthase (FASN) g. 16024 (A>G), Stearoyl-CoA desaturase (SCD) g. 10329 (C>T), and pleomorphic adenoma gene (PLAG1) g. 25003338 (C>G) genotypic and allelic polymorphisms were evaluated, along with their associations with fatty acid composition, adipogenic gene expression, and carcass characteristics (carcass weight, yield grade, backfat thickness, and marbling score) in Hanwoo steers. A total of 128 Hanwoo steers were selected for this study and the Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to identify polymorphism of these genes. The AG genotype and G allele in FASN g. 16024 (A>G), CT genotype and T allele in SCD g. 10329 (C>T), and GG genotype and G allele in PLAG1 g. 25003338 (C>G) showed higher frequency and positively correlated with carcass traits, yield, and quality grades. Fatty acid composition results indicate that C18:3n-6, C20:1, and C20:2n-6 were significantly higher in the AA genotype of FASN gene, C14:1 and C18:3n-6 in the CC genotype, and C16:1 in the TT genotype of SCD gene. C12:0, C14:0, C16:1, C18:0, and C20:0 were higher in the CC genotype of PLAG1 gene. Furthermore, RT-qPCR analysis of adipogenesis-related genes (AMP-activated protein kinase-α (AMPKα), Carnitine palmitoyl transferase-1β (CPT1), G-coupled protein receptor-43 (GPR43), and SCD) across different SNP genotypes suggests a systemic interaction between genetic factors and adipogenesis in beef cattle. This study emphasizes the significance of FASN g. 16024 (A>G), SCD g. 10329 (C>T), and PLAG1 g. 25003338 (C>G) SNPs for genetic selection to enhance beef quality and elucidate lipid metabolic pathways in Hanwoo cattle.
Collapse
Affiliation(s)
- Jia Yu
- Department of Animal Science, Chungbuk National University, Cheongju 28644, Republic of Korea; (J.Y.); (Y.C.); (T.L.)
| | - Sajida Naseem
- Engineering Research Center of North-East Cold Region Beef Cattle Science & Technology Innovation Ministry of Education, Department of Animal Science, Yanbian University, Yanji 133002, China;
| | - Sungkwon Park
- Department of Food Science and Biotechnology, Sejong University, Seoul 05006, Republic of Korea;
| | - Sunjin Hur
- Department of Animal Science and Technology, Chung-Ang University, Anseong 17546, Republic of Korea;
| | - Yoonbin Choi
- Department of Animal Science, Chungbuk National University, Cheongju 28644, Republic of Korea; (J.Y.); (Y.C.); (T.L.)
| | - Teahyung Lee
- Department of Animal Science, Chungbuk National University, Cheongju 28644, Republic of Korea; (J.Y.); (Y.C.); (T.L.)
| | - Xiangzi Li
- Engineering Research Center of North-East Cold Region Beef Cattle Science & Technology Innovation Ministry of Education, Department of Animal Science, Yanbian University, Yanji 133002, China;
| | - Seongho Choi
- Department of Animal Science, Chungbuk National University, Cheongju 28644, Republic of Korea; (J.Y.); (Y.C.); (T.L.)
| |
Collapse
|
32
|
Navalho S, Ferrer-Ledo N, Barbosa MJ, Varela J. Nannochloropsis Lipids and Polyunsaturated Fatty Acids: Potential Applications and Strain Improvement. Mar Drugs 2025; 23:128. [PMID: 40137314 PMCID: PMC11943726 DOI: 10.3390/md23030128] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/20/2025] [Revised: 03/11/2025] [Accepted: 03/14/2025] [Indexed: 03/27/2025] Open
Abstract
The genus Nannochloropsis comprises a group of oleaginous microalgae that accumulate polyunsaturated fatty acids (PUFAs), especially eicosapentaenoic acid (EPA). These molecules are essential for the correct development and health of humans and animals. Thanks to their attractive lipid profile, Nannochloropsis is mainly marketed as a feed ingredient in aquaculture. In microalgae of this genus, contents and cellular location of PUFAs are affected by the growth conditions and gene expression. Strain improvement through non-recombinant approaches can generate more productive strains and efficient bioprocesses for PUFA production. Nevertheless, the lack of specific markers, detection methods, and selective pressure for isolating such mutants remains a bottleneck in classical mutagenesis approaches or lipid quality assessment during cultivation. This review encompasses the importance of PUFAs and lipid classes from Nannochloropsis species and their potential applications. Additionally, a revision of the different ways to increase PUFA content in Nannochloropsis sp. by using classical mutagenesis and adaptive laboratory evolution is also presented, as well as various methods to label and quantify lipids and PUFAs from Nannochloropsis microalgae.
Collapse
Affiliation(s)
- Sofia Navalho
- GreenCoLab—Associação Oceano Verde, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal;
- Bioprocess Engineering, AlgaePARC, Wageningen University and Research, P.O. Box 16, 6700 AA Wageningen, The Netherlands; (N.F.-L.); (M.J.B.)
- CCMAR—Centre of Marine Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
| | - Narcis Ferrer-Ledo
- Bioprocess Engineering, AlgaePARC, Wageningen University and Research, P.O. Box 16, 6700 AA Wageningen, The Netherlands; (N.F.-L.); (M.J.B.)
| | - Maria J. Barbosa
- Bioprocess Engineering, AlgaePARC, Wageningen University and Research, P.O. Box 16, 6700 AA Wageningen, The Netherlands; (N.F.-L.); (M.J.B.)
| | - João Varela
- GreenCoLab—Associação Oceano Verde, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal;
- CCMAR—Centre of Marine Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
| |
Collapse
|
33
|
Yan D, Hou Y, Lei X, Xiao H, Zeng Z, Xiong W, Fan C. The Impact of Polyunsaturated Fatty Acids in Cancer and Therapeutic Strategies. Curr Nutr Rep 2025; 14:46. [PMID: 40085324 DOI: 10.1007/s13668-025-00639-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 03/06/2025] [Indexed: 03/16/2025]
Abstract
PURPOSE OF REVIEW Cancer is a disease influenced by both genetic and environmental factors, with dietary lipids being a significant contributing factor. This review summarizes the role of polyunsaturated fatty acids (PUFAs) in the mechanism of tumor occurrence and development, and elucidate the role of PUFAs in tumor treatment. RECENT FINDINGS PUFAs exert their impact on cancer through altering lipid composition in cell membranes, interacting with cell membrane lipid receptors, directly modulating gene expression in the cell nucleus, and participating in the metabolism of lipid mediators. Most omega-3 PUFAs are believed to inhibit cell proliferation, promote cancer cell death, suppress cancer metastasis, alter energy metabolism, inhibit tumor microenvironment inflammation, and regulate immune responses involving macrophages, T cells, NK cells, and others. However, certain omega-6 PUFAs exhibit weaker anti-tumor effects and may even promote tumor development, such as by fostering inflammatory tumor microenvironment and enhancing tumor cell proliferation. PUFAs play important roles in hallmarks of cancer including tumor cell proliferation, cell death, migration and invasion, energy metabolism remodeling, epigenetics, and immunity. These findings provide insights into the mechanisms of cancer development and offers options for dietary management of cancer.
Collapse
Affiliation(s)
- Dong Yan
- Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China
| | - Yingshan Hou
- Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China
| | - Xinyi Lei
- Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China
| | - Hao Xiao
- Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China
| | - Zhaoyang Zeng
- Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, Hunan, China
| | - Wei Xiong
- Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, Hunan, China
| | - Chunmei Fan
- Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan Province, China.
- Department of Histology and Embryology, School of Basic Medicine Sciences, Central South University, Changsha, 410013, Hunan Province, China.
| |
Collapse
|
34
|
Wang H, Zhang C, Sun Y, Sun S, Wang Z, Xiang H. Inverse association of dietary consumption of n3 and n6 fatty acids with hyperuricemia among adults. PLoS One 2025; 20:e0317490. [PMID: 40080475 PMCID: PMC11906074 DOI: 10.1371/journal.pone.0317490] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/13/2024] [Accepted: 12/30/2024] [Indexed: 03/15/2025] Open
Abstract
BACKGROUND The precise link between dietary consumption of n-3 and n-6 fatty acids and hyperuricemia remains equivocal. Accordingly, the purpose of the current investigation is to clarify any possible associations between the consumption of n-3 and n-6 fatty acids and hyperuricemia in the context of American adults. MATERIALS AND METHODS The present investigation employed a cross-sectional design, comprising a sample of 21,120 American adults above the age of 20 from the National Health and Nutrition Examination Survey (NHANES) waves between 2007 and 2016. The dietary consumption of n-3 and n-6 fatty acids was measured through two 24-h dietary recall interviews. To assess the relationships of dietary consumption of n3 and n6 fatty acids with hyperuricemia, we applied multivariable logistic regression, t tests, chi-square tests, and restricted cubic spline. To determine the robustness of our findings, sensitivity analyses were also carried out. RESULTS The results of the multivariable logistic regression models indicated a significant correlation between dietary consumption of n3 and n6 fatty acids and hyperuricemia. The ORs with 95% CIs of hyperuricemia for the highest tertile versus lowest tertile of dietary consumption of n3 and n6 fatty acids were 0.76 (0.66, 0.88) (p < 0.001) and 0.72 (0.64, 0.82) (p < 0.001), respectively. Moreover, dose‒response analyses revealed a linear relationship between n-3 and n-6 fatty acid consumption and the risk of hyperuricemia. CONCLUSION The findings of this study indicate a significant inverse correlation between the dietary consumption of n3 and n6 fatty acids and hyperuricemia in the US adult population. Notably, there was no significant relationship between the n6:n3 ratio and hyperuricemia.
Collapse
Affiliation(s)
- Huakai Wang
- Department of General Surgery, Pudong New Area People’s Hospital, Shanghai, China
| | - Chao Zhang
- Qingdao Medical College, Qingdao University, Qingdao , China
| | - Yuxin Sun
- . Department of Oncology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
| | - Sirui Sun
- The Hockaday School, Dallas, Texas, United States of America
| | - Zhe Wang
- Department of General Surgery, Pudong New Area People’s Hospital, Shanghai, China
| | - Honggang Xiang
- Department of General Surgery, Pudong New Area People’s Hospital, Shanghai, China
| |
Collapse
|
35
|
Idyryshev B, Muratbayev A, Tashybayeva M, Spanova A, Amirkhanov S, Serikova A, Serikov Z, Bakirova L, Jumazhanova M, Bepeyeva A. Development and Characterization of Emulsion Gels with Pine Nut Oil, Inulin, and Whey Proteins for Reduced-Fat Meat Products. Foods 2025; 14:962. [PMID: 40231973 PMCID: PMC11941322 DOI: 10.3390/foods14060962] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/22/2025] [Revised: 03/07/2025] [Accepted: 03/09/2025] [Indexed: 04/16/2025] Open
Abstract
An emulsion gel was developed to replace animal fats in meat products while preserving desirable sensory and structural attributes. The gel was prepared by emulsifying pine nut oil and sunflower oil with whey protein concentrate (WPC) and polysaccharides (inulin and carrageenan). Process parameters, including the inulin-to-water ratio, homogenization speed, and temperature, were optimized to achieve stable gels exhibiting high water- and fat-binding capacities. Scanning electron micrographs revealed a cohesive network containing uniformly dispersed lipid droplets, with carrageenan promoting a denser matrix. Chemical assessments demonstrated a notably lower saturated fatty acid content (10.85%) and only 0.179% trans-isomers, alongside an elevated proportion (71.17%) of polyunsaturated fatty acids. This fatty acid profile suggests potential cardiovascular health benefits compared with conventional animal fats. Texture analyses showed that carrageenan increased gel strength and hardness; Experiment 4 recorded values of 15.87 N and 279.62 N, respectively. Incorporation of WPC at moderate levels (3-4%) further enhanced the yield stress, reflecting a robust protein-polysaccharide network. These findings indicate that the developed emulsion gel offers a viable alternative to animal fats in meat products, combining superior nutritional attributes with acceptable textural properties. The substantial polyunsaturated fatty acid content and minimal trans-isomers, coupled with the gel's mechanical stability, support the feasibility of creating reduced-fat, functional formulations that align with consumer demands for healthier alternatives.
Collapse
Affiliation(s)
| | - Alibek Muratbayev
- Department of “Food Technologies”, Shakarim University, 20A Glinki Street, Semey 071412, Kazakhstan; (B.I.); (M.T.); (A.S.); (S.A.); (A.S.); (Z.S.); (L.B.); (M.J.); (A.B.)
| | | | | | | | | | | | | | | | | |
Collapse
|
36
|
Karakas H, Cagman Z, Kizilarslan-Hancer C, Erol E. Isolation and Characterization of Secondary Metabolites from Endemic and Edible Polygonum sivasicum with In Vitro Antioxidant and Cytotoxic Activities. ACS OMEGA 2025; 10:9756-9767. [PMID: 40092762 PMCID: PMC11904701 DOI: 10.1021/acsomega.5c00438] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Grants] [Track Full Text] [Figures] [Subscribe] [Scholar Register] [Received: 01/15/2025] [Revised: 02/12/2025] [Accepted: 02/19/2025] [Indexed: 03/19/2025]
Abstract
Polygonum sivasicum Kit Tan and Yildiz, one of the eight endemic Polygonum species in Türkiye, belongs to the Polygonaceae family. Preliminary phytochemical investigation of methanol and hexane extracts of P. sivasicum resulted in four compounds, namely, annphenone (1), hyperoside (2), daucosterol (3), and β-sitosterol (4). Their structures were elucidated by 1D-, 2D-NMR, and HRESIMS analyses. This study signifies the first isolation of annphenone from the Polygonum genus. Antioxidant capabilities of different extracts of P. sivasicum were carried out using DPPH·, ABTS·+, CUPRAC, metal chelating, and β-carotene linoleic acid bleaching assays, and their effectiveness was quantified through IC50 values. Furthermore, 27 phenolic compounds were identified using LC-HRESIMS from methanol extract, which has the highest antioxidant activity among the P. sivasicum extracts. The major phenolic constituents identified were hyperoside (4535.0 μg/g extract), rutin (4387.4 μg/g extract), and chlorogenic acid (3306.6 μg/g extract). GC-MS analysis determined palmitic acid, α-linolenic acid, and 8,11-octadecadieonic acid as major fatty acids in the hexane extract. The cell viability profile of P. sivasicum methanol extract and its isolates hyperoside, annphenone, and daucosterol was evaluated on fibroblast (CCD-1079Sk), breast carcinoma (MCF-7) and lung carcinoma (A549) cell lines. Annphenone exhibited IC50 values of 0.25 ± 0.01 mg/mL against the A549 cell line and 0.36 ± 0.02 mg/mL against the MCF-7 cell line. The selective cytotoxicity observed for daucosterol against the A549 cell line, with a high selectivity index of 1.44, underscores its potential as a promising candidate for drug development. The study establishes a framework integrating phytochemical profiling with biological assays to identify therapeutic agents from endemic plants.
Collapse
Affiliation(s)
- Humeyra Karakas
- Department
of Pharmacognosy and Natural Products Chemistry, Health Sciences Institute, Bezmialem Vakif University, 34093 Istanbul, Turkey
| | - Zeynep Cagman
- Department
of Biochemistry, Faculty of Pharmacy, Bezmialem
Vakif University, 34093 Istanbul, Turkey
| | - Cagla Kizilarslan-Hancer
- Department
of Pharmaceutical Botany, Faculty of Pharmacy, Bezmialem Vakif University, 34093 Istanbul, Turkey
| | - Ebru Erol
- Department
of Analytical Chemistry, Faculty of Pharmacy, Bezmialem Vakif University, 34093 Istanbul, Turkey
| |
Collapse
|
37
|
Niu Y, Li W, Yang Y, Wang H, He Z, Qin H, Zhang Y, Hu D, Wang J, Zhang C, Yang G, Bancroft I, Zou J. Creation of rapeseed germplasm with high polyunsaturated fatty acid content by wild-relative introgression from Brassica carinata. PLANT COMMUNICATIONS 2025; 6:101193. [PMID: 39550611 PMCID: PMC11956087 DOI: 10.1016/j.xplc.2024.101193] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Subscribe] [Scholar Register] [Received: 07/14/2023] [Revised: 08/30/2024] [Accepted: 11/15/2024] [Indexed: 11/18/2024]
Affiliation(s)
- Yan Niu
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Wenwen Li
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Yinghui Yang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Hao Wang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Zhesi He
- Department of Biology, University of York, Heslington, York YO10 5DD, UK
| | - Han Qin
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Yikai Zhang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Dandan Hu
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Jing Wang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Chunyu Zhang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Guangsheng Yang
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China
| | - Ian Bancroft
- Department of Biology, University of York, Heslington, York YO10 5DD, UK.
| | - Jun Zou
- National Key Laboratory of Crop Genetic Improvement, College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.
| |
Collapse
|
38
|
Mandal AK, Parida S, Behera AK, Adhikary SP, Lukatkin AA, Lukatkin AS, Jena M. Seaweed in the Diet as a Source of Bioactive Metabolites and a Potential Natural Immunity Booster: A Comprehensive Review. Pharmaceuticals (Basel) 2025; 18:367. [PMID: 40143143 PMCID: PMC11945151 DOI: 10.3390/ph18030367] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/19/2024] [Revised: 02/15/2025] [Accepted: 02/19/2025] [Indexed: 03/28/2025] Open
Abstract
Seaweed plays an essential role in the survival of marine life, provides habitats and helps in nutrient recycling. It is rich in valuable nutritious compounds such as pigments, proteins, polysaccharides, minerals, vitamins, omega-rich oils, secondary metabolites, fibers and sterols. Pigments like fucoxanthin and astaxanthin and polysaccharides like laminarin, fucoidan, galactan and ulvan possess immune-modulatory and immune-enhancing properties. Moreover, they show antioxidative, antidiabetic, anticancer, anti-inflammatory, antiproliferative, anti-obesity, antimicrobial, anticoagulation and anti-aging properties and can prevent diseases such as Alzheimer's and Parkinson's and cardiovascular diseases. Though seaweed is frequently consumed by Eastern Asian countries like China, Japan, and Korea and has gained the attention of Western countries in recent years due to its nutritional properties, its consumption on a global scale is very limited because of a lack of awareness. Thus, to incorporate seaweed into the global diet and to make it familiar as a functional food, issues such as large-scale cultivation, processing, consumer acceptance and the development of seaweed-based food products need to be addressed. This review is intended to give a brief overview of the present status of seaweed, its nutritional value and its bioactive metabolites as functional foods for human health and diseases owing to its immunity-boosting potential. Further, seaweed as a source of sustainable food and its prospects along with its issues are discussed in this review.
Collapse
Affiliation(s)
- Amiya Kumar Mandal
- Algal Biotechnology and Molecular Systematic Laboratory, Post Graduate Department of Botany, Berhampur University, Bhanja Bihar, Berhampur 760007, Odisha, India; (A.K.M.); (S.P.); (A.K.B.)
| | - Sudhamayee Parida
- Algal Biotechnology and Molecular Systematic Laboratory, Post Graduate Department of Botany, Berhampur University, Bhanja Bihar, Berhampur 760007, Odisha, India; (A.K.M.); (S.P.); (A.K.B.)
| | - Akshaya Kumar Behera
- Algal Biotechnology and Molecular Systematic Laboratory, Post Graduate Department of Botany, Berhampur University, Bhanja Bihar, Berhampur 760007, Odisha, India; (A.K.M.); (S.P.); (A.K.B.)
| | - Siba Prasad Adhikary
- Department of Biotechnology, Institute of Science, Visva-Bharati, Santiniketan 731235, West Bengal, India;
| | - Andrey A. Lukatkin
- Department of Cytology, Histology and Embryology with Courses in Medical Biology and Molecular Cell Biology, N.P. Ogarev Mordovia State University, Bolshevistskaja Str., 68, Saransk 430005, Russia;
| | | | - Mrutyunjay Jena
- Algal Biotechnology and Molecular Systematic Laboratory, Post Graduate Department of Botany, Berhampur University, Bhanja Bihar, Berhampur 760007, Odisha, India; (A.K.M.); (S.P.); (A.K.B.)
| |
Collapse
|
39
|
Martín-Olmedo JJ, Jurado-Fasoli L. Impact of technological processing on the bioavailability of omega-3 fatty acids in fish oil: a review. Crit Rev Food Sci Nutr 2025:1-11. [PMID: 40025684 DOI: 10.1080/10408398.2025.2472858] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/04/2025]
Abstract
Both the growing prevalence of chronic diseases and the consumer's health awareness have increased the intake of fish oil supplements since it is rich in omega-3. However, the proposed preventive or therapeutic effects of fish oil in different diseases are inconsistent, partially because processing affects on omega-3 stability and bioavailability. Thus, this review aims to describe the influence of fish oil processing on the omega-3 bioavailability in humans. This review illustrates how fish oil is obtained and processed, summarizes how omega-3 bioavailability is assessed, and describes how the molecular form and formulation may modulate their bioavailability. The bioavailability of omega-3 depends on the processing and formulation of fish oil, which influences the acceptability and stability of the final product. Currently, omega-3 is more bioavailable when ingested as free fatty acid, followed by triglyceride, and lastly as ethyl ester. Due to their high susceptibility to oxidation and preliminary findings, administering omega-3 in the form of triglyceride may be the most suitable to maximize bioavailability. Additionally, formulations that promote self-emulsification of fish oil show promise, though more human studies are needed to support these results. These results could optimize the bioavailability of omega-3 and the potential health-related applications of fish oil.
Collapse
Affiliation(s)
- Juan J Martín-Olmedo
- Department of Physiology, Faculty of Medicine, University of Granada, Granada, Spain
- Department of Physical and Sports Education, Faculty of Sport Sciences, Sport and Health University Research Institute (iMUDS), University of Granada, Granada, Spain
| | - Lucas Jurado-Fasoli
- Department of Physiology, Faculty of Medicine, University of Granada, Granada, Spain
- Department of Physical and Sports Education, Faculty of Sport Sciences, Sport and Health University Research Institute (iMUDS), University of Granada, Granada, Spain
| |
Collapse
|
40
|
Oteyola AO, Oliveira IMSD, Almeida JMD, Cardoso LC, Paula TDMDE, Nogueira JM, Carvalho JCDS, Nogueira HM, Porto BLS, Mota APL, Campos-Junior PHA, Jorge EC, Almeida FRCLD. Chronic fat consumption affects metabolic aspects of murine physiology and influences ovarian follicle atresia. Reprod Toxicol 2025; 132:108836. [PMID: 39800278 DOI: 10.1016/j.reprotox.2025.108836] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/20/2024] [Revised: 01/09/2025] [Accepted: 01/09/2025] [Indexed: 01/15/2025]
Abstract
Saturated fat has been linked to cardiovascular diseases, leading to an increase in polyunsaturated fat consumption. The aim of the present study was to investigate the effects of three fat sources (coconut oil, lard and soybean oil) on metabolic and reproductive parameters in heterogenic mice. Female Swiss mice (5-6 weeks old; n = 9/group) were divided into four experimental groups: control (CC), coconut oil (CO), lard (LA), and soybean oil (SO), and were orally given 0.6 mL of the corresponding fat daily for 6 weeks to further investigate morphological, biochemical, and molecular parameters. SO females showed the highest glucose intolerance (P < 0.05), and all experimental groups were highly insulin resistant, with no statistical differences among them (P > 0.05). Moreover, all fat supplemented groups presented increased proportion in bile ducts, and CO and SO females presented higher LDL-cholesterol levels compared to CC (P < 0.05). Regarding reproductive parameters, estrous cycle alterations were observed mainly in the SO group, showing extended luteal phase duration (longer diestrus), and higher numbers of atretic follicles per area compared to the CC females (P < 0.05). Furthermore, higher proportion of active Casp-3 positive cells in the granulosa layers of preantral follicles were observed in the LA compared to the CO group (P < 0.05). The gene expression data revealed downregulation of Igf1r and Acvr1 in SO, upregulation of Igf1r in LA and Lhcgr in CO compared to CC females (P < 0.05). Thus, excessive fat intake may have deleterious effects on metabolism and reproductive function, but lard may be the least harmful source.
Collapse
Affiliation(s)
- Ayodeji Ojo Oteyola
- Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | | | - Jonathas Medeiros de Almeida
- Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | - Lucas Carvalho Cardoso
- Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | | | - Julia Meireles Nogueira
- Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | | | | | | | - Ana Paula Lucas Mota
- Department of Clinical Analysis, Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | | | - Erika Cristina Jorge
- Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
| | | |
Collapse
|
41
|
Valenzuela R, Metherel AH, Cisbani G, Smith ME, Chouinard-Watkins R, Klievik BJ, Farias C, Videla LA, Bazinet RP. Specific activity of mouse liver desaturases and elongases: Time course effects using n-3 and n-6 PUFA substrates and inhibitory responses of delta-6 desaturase. Biochim Biophys Acta Mol Cell Biol Lipids 2025; 1870:159594. [PMID: 39798684 DOI: 10.1016/j.bbalip.2025.159594] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/04/2024] [Revised: 12/17/2024] [Accepted: 01/07/2025] [Indexed: 01/15/2025]
Abstract
The synthesis of n-3 and n-6 polyunsaturated acids (PUFAs) is associated with physiological functions in mammals, being catalyzed by Δ-5D and Δ-6D desaturases and elongases Elovl-2 and Elovl-5. In this context, we aimed to study the chief kinetic features of PUFA liver anabolism, looking upon (i) the time-dependency for the specific activity of Δ-6D, Δ-5D, Elovl2, Elovl2/5 and Elovl5, using n-3 and n-6 precursors between 0 and 240 min ex vivo in mouse liver.; and (ii) the specific activity-substrate (α-linolenic acid; ALA) concentration responses of Δ-6D in the absence and presence of linoleic acid (LA), arachidonic acid (ARA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), an enzyme regarded as the rate-limiting step in PUFA anabolism. Mouse liver was obtained from eight-week-old Balb/c mice fed a chow diet (expressed as % of total calories: 18 % fat, 24 % protein, and 58 % carbohydrate, with a caloric value of 3.1 kcal/g) for eight weeks, and used for preparation of the microsomal fraction. Enzymatic activities assayed under the addition of specific PUFA precursors or LA, ARA, EPA and DHA, identifying the respective PUFA products as fatty acid methyl esters by gas chromatographic analysis. Data described corroborate that (i) PUFA metabolism mainly occurs in the liver, with the participating enzymes preferring n-3 than n-6 substrates; and show that (ii) the rate-limiting step of PUFA metabolism relies on the second reaction of Δ-6D (24:5n-3 transformed to 24:6n-3); and (iii) LA, ARA, EPA and DHA act as non-competitive inhibitors with respect to ALA in the reaction catalyzed by Δ-6D. These results are relevant for future studies concerning the metabolic and nutritional implications of changes in desaturation and elongation of PUFAs.
Collapse
Affiliation(s)
- Rodrigo Valenzuela
- Nutrition Department, Faculty of Medicine, University of Chile, Santiago, Chile; Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada.
| | - Adam H Metherel
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Giulia Cisbani
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Mackenzie E Smith
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Raphaël Chouinard-Watkins
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Brinley J Klievik
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Camila Farias
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| | - Luis A Videla
- Molecular and Clinical Pharmacology Program, Institute of Biomedical Sciences, Faculty of Medicine, University of Chile, Santiago, Chile
| | - Richard P Bazinet
- Department of Nutritional Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada
| |
Collapse
|
42
|
Bekele B, Andargie M, Gallach M, Beyene D, Tesfaye K. Decoding gene expression dynamics during seed development in sesame (Sesamum indicum L.) through RNA-Seq analysis. Genomics 2025; 117:110997. [PMID: 39809365 DOI: 10.1016/j.ygeno.2025.110997] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/06/2024] [Revised: 01/09/2025] [Accepted: 01/10/2025] [Indexed: 01/16/2025]
Abstract
Sesame (Sesamum indicum L., 2n = 2× = 26) from the Pedaliaceae family is primarily grown for its high oil content, rich in unsaturated fatty acids like linoleic acid (LA) and alpha-linolenic acid (ALA). However, the molecular mechanisms of sesame oil accumulation remain poorly understood. This study analyzed transcriptomes at two seed development stages: Young Stage (YS, pods 1.5-2.5 cm) and Mature Stage (MS, brown pods >2.5 cm), to explore regulatory mechanisms and identify key genes involved in lipid biosynthesis. From 25,173 genes, 18,820 with expression values >10 CPM in at least 70 % of replicates were included in differential expression (DE) analysis. Active expression (LFC > 0) was observed in 9372 and 9448 genes at YS and MS, respectively. DEGs were annotated, revealing roles in various biological processes, (e.g., mRNA metabolic process, reproduction-related developmental processes, seed development), molecular functions (e.g., aminoacyltransferase activity, ubiquitin-like protein and ubiquitin-protein transferase activities), and cellular components (e.g., peroxisome, microbody, lipid droplet). KEGG analysis highlighted genes involved in fatty acid synthesis (e.g., fabG, fabZ), TAG biosynthesis (DGAT1, GPAT), and alpha-linolenic acid metabolism (AOS, LCAT3). Key genes upregulated at MS included SIN_1025205 (protein transport), SIN_1006853 (acetylajmalan esterase), and SIN_1003267 (gamma-cadinene synthase). The study generated a valuable transcriptome dataset and gene list for seed development and lipid biosynthesis, which will be validated through functional studies. An interactive webpage is provided for data exploration.
Collapse
Affiliation(s)
- Bantayehu Bekele
- Department of Microbial, Cellular, and molecular biology, Addis Ababa University, Addis Ababa, Ethiopia.; Biology Department, Oda bultum University, Chiro, Ethiopia.
| | | | | | - Dereje Beyene
- Department of Microbial, Cellular, and molecular biology, Addis Ababa University, Addis Ababa, Ethiopia
| | - Kassahun Tesfaye
- Department of Microbial, Cellular, and molecular biology, Addis Ababa University, Addis Ababa, Ethiopia
| |
Collapse
|
43
|
Aronson WJ, Grogan T, Liang P, Jardack P, Liddell AR, Perez C, Elashoff D, Said J, Cohen P, Marks LS, Henning SM. High Omega-3, Low Omega-6 Diet With Fish Oil for Men With Prostate Cancer on Active Surveillance: The CAPFISH-3 Randomized Clinical Trial. J Clin Oncol 2025; 43:800-809. [PMID: 39671538 PMCID: PMC11869882 DOI: 10.1200/jco.24.00608] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/21/2024] [Revised: 09/20/2024] [Accepted: 10/30/2024] [Indexed: 12/15/2024] Open
Abstract
PURPOSE Men on active surveillance (AS) for prostate cancer are extremely interested in dietary changes or supplements to prevent progression of their disease. We sought to determine whether a high omega-3, low omega-6 fatty acid diet with fish oil capsules (D + FO) decreases proliferation (Ki-67) in prostate biopsies in men with prostate cancer on AS over a 1-year time period. METHODS In this phase II, prospective randomized trial, men (N = 100) with grade group 1 or 2 prostate cancer who elected AS were randomly assigned to the D + FO or a control group. Same-site prostate biopsies were obtained at baseline and 1 year. The primary end point was the change in Ki-67 index from baseline to 1 year from same-site biopsies compared between the groups. RESULTS The Ki-67 index decreased in the D + FO group by approximately 15% from baseline to 1 year (1.34% at baseline, 1.14% at 1 year) and increased in the control group by approximately 24% from baseline to 1 year (1.23% at baseline, 1.52% at 1 year), resulting in a statistically significant difference in the change of Ki-67 index between the groups (95% CI, 2% to 52%, P = .043). There was no significant difference in the secondary outcomes grade group, tumor length, Decipher genomic score, or prostate-specific antigen between the two groups. Four patients in the D + FO group were withdrawn from the trial because of adverse events related to the FO. CONCLUSION A high omega-3, low omega-6 diet with FO for 1 year resulted in a significant reduction in Ki-67 index, a biomarker for prostate cancer progression, metastasis, and death. These findings support future phase III trials incorporating this intervention in men on AS.
Collapse
Affiliation(s)
- William J. Aronson
- Department of Urology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
- VA Medical Center Greater Los Angeles Healthcare System, Los Angeles, California
| | - Tristan Grogan
- Department of Medicine Statistics Core, David Geffen School of Medicine, University of California Los Angeles, Los Angeles; California
| | - Pei Liang
- Department of Urology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
| | - Patricia Jardack
- Clinical Translational Science Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles; California
| | - Amana R. Liddell
- Department of Urology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
| | - Claudia Perez
- Department of Medicine Statistics Core, David Geffen School of Medicine, University of California Los Angeles, Los Angeles; California
| | - David Elashoff
- Department of Medicine Statistics Core, David Geffen School of Medicine, University of California Los Angeles, Los Angeles; California
| | - Jonathan Said
- Department of Pathology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
| | - Pinchas Cohen
- Leonard Davis School of Gerontology, University of Southern California, Los Angeles, California
| | - Leonard S. Marks
- Department of Urology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
| | - Susanne M. Henning
- Department of Urology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California
| |
Collapse
|
44
|
Santamarina AB, Moreira RG, Mennitti LV, Martins Ferreira YA, Jucá A, Prado CM, Pisani LP. Low-carbohydrate diet enriched with omega-3 and omega-9 fatty acids modulates inflammation and lipid metabolism in the liver and white adipose tissue of a mouse model of obesity. Nutr Metab Cardiovasc Dis 2025:103932. [PMID: 40089393 DOI: 10.1016/j.numecd.2025.103932] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/30/2024] [Revised: 02/14/2025] [Accepted: 02/18/2025] [Indexed: 03/17/2025]
Abstract
BACKGROUND AND AIM The low-carbohydrate high-fat (LCHF) diet lipids are often overlooked for obesity management. We hypothesized that unsaturated lipids enhance fatty acid metabolism, and influence obesity-related metainflammation. METHODS AND RESULTS Male Swiss mice were fed an obesity-inducing diet for ten weeks. Subsequently, the obese mice were divided into four groups, each receiving a LCHF diet enriched with different types of lipids: saturated fatty acids (SFA), polyunsaturated fatty acids (PUFA) ω-3, PUFA ω-6, and monounsaturated fatty acids (MUFA) ω-9 during six weeks as an obesity intervention. For comparison, a lean control (CTL) group and an obesity control (HFC) group were also included, spanning the entire 16-week experimental protocol. We evaluated body mass gain, fatty acid profiles via gas chromatography, elongase, and desaturase activities, NFκBp65 expression by western blotting, and cytokine by ELISA kits in serum, liver, and retroperitoneal adipose tissue (RET) samples. Our results highlight that ω-3 and ω-9 LCHF diets facilitate weight loss and enhance unsaturated fatty acid incorporation in liver, RET, and serum compared to the other groups. The ω-3 LCHF diet notably reduced the ω-6/ω-3 ratio and improved inflammatory status by reducing cytokines such as IL-4, IL-17, IL-33, CXCL1/KC, and inhibiting NFκBp65 activity compared to the HFC group. Desaturase (delta-9 desaturase-18, delta-6 desaturase) and elongase (ELOVL5 and ELOVL6) activities were modulated in liver, RET, and serum samples by ω-3 and ω-9 compared to the HFC group. CONCLUSIONS ω-3 and ω-9 fats were most effective in obesity treatment with the LCHF diet, highlighting the significance of lipid type in carbohydrate-restriction for obesity management.
Collapse
Affiliation(s)
- Aline Boveto Santamarina
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil
| | - Renata Guimarães Moreira
- Laboratório de Metabolismo e Reprodução de Organismos Aquáticos (LAMEROA), Instituto de Biociências (IB), Universidade de São Paulo (USP), Brazil
| | - Laís Vales Mennitti
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil
| | - Yasmin Alaby Martins Ferreira
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil
| | - Andrea Jucá
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil
| | - Carla Máximo Prado
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil
| | - Luciana Pellegrini Pisani
- Biosciences Department, Institute of Health and Society, Federal University of São Paulo, Campus Baixada Santista, UNIFESP, Santos, São Paulo, Brazil.
| |
Collapse
|
45
|
Fukuishi N, Takahama K, Kurosaki H, Ono S, Asai H. The Role of Endogenous Specialized Proresolving Mediators in Mast Cells and Their Involvement in Inflammation and Resolution. Int J Mol Sci 2025; 26:1491. [PMID: 40003957 PMCID: PMC11855587 DOI: 10.3390/ijms26041491] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/15/2025] [Revised: 02/05/2025] [Accepted: 02/10/2025] [Indexed: 02/27/2025] Open
Abstract
Many polyunsaturated fatty acids within cells exhibit diverse physiological functions. Particularly, arachidonic acid is the precursor of highly bioactive prostaglandins and leukotrienes, which are pro-inflammatory mediators. However, polyunsaturated fatty acids, such as arachidonic, docosahexaenoic, and eicosapentaenoic acids, can be metabolized into specialized proresolving mediators (SPMs), which have anti-inflammatory properties. Given that pro-inflammatory mediators and SPMs are produced via similar enzymatic pathways, SPMs can play a crucial role in mitigating excessive tissue damage induced by inflammation. Mast cells are immune cells that are widely distributed and strategically positioned at interfaces with the external environment, such as the skin and mucosa. As immune system sentinels, they respond to harmful pathogens and foreign substances. Upon activation, mast cells release various pro-inflammatory mediators, initiating an inflammatory response. Furthermore, these cells secrete factors that promote tissue repair and inhibit inflammation. This dual function positions mast cells as central regulators, balancing between the body's defense mechanisms and the need to minimize tissue injury. This review investigates the production of SPMs by mast cells and their subsequent effects on these cells. By elucidating the intricate relationship between mast cells and SPMs, this review aims to provide a comprehensive understanding of the mechanism by which these cells regulate the delicate balance between tissue damage and repair at inflammatory sites, ultimately contributing to the resolution of inflammatory responses.
Collapse
Affiliation(s)
- Nobuyuki Fukuishi
- Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kinjo Gakuin University, Nagoya 463-8521, Japan; (H.K.); (S.O.); (H.A.)
| | - Kentaro Takahama
- Technology Center, Tokai National Higher Education and Research System, Nagoya 464-8601, Japan;
| | - Hiromasa Kurosaki
- Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kinjo Gakuin University, Nagoya 463-8521, Japan; (H.K.); (S.O.); (H.A.)
| | - Sayaka Ono
- Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kinjo Gakuin University, Nagoya 463-8521, Japan; (H.K.); (S.O.); (H.A.)
| | - Haruka Asai
- Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kinjo Gakuin University, Nagoya 463-8521, Japan; (H.K.); (S.O.); (H.A.)
| |
Collapse
|
46
|
Zhang D, Zhao Z. Selection of Key Genes for Apricot Kernel Oil Synthesis Based on Transcriptome Analysis. Foods 2025; 14:568. [PMID: 40002012 PMCID: PMC11854223 DOI: 10.3390/foods14040568] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/06/2025] [Revised: 02/07/2025] [Accepted: 02/07/2025] [Indexed: 02/27/2025] Open
Abstract
The purpose of this study was to identify the key genes regulating apricot kernel oil (AKO) biosynthesis and understand the molecular pathways of AKO synthesis and accumulation. This study used two varieties of apricot kernel to determine the oil contents and primary fatty acid compositions at different developmental stages. Candidate genes for AKO biosynthesis were selected through transcriptome sequencing technology and weighted gene co-expression network analysis (WGCNA), and these genes were verified by quantitative reverse transcription polymerase chain reaction (qRT-PCR). The results indicate that during apricot ripening, the content of AKO exhibits an 'S'-shaped accumulation pattern. The primary fatty acid components are C18:1 and C18:2. The transcriptome sequencing produced 164.19 Gb of clean data and 17,411 differentially expressed genes. The WGCNA results indicate that significantly differentially expressed genes cluster into seven modules-gene clusters (module)-with the strongest correlations to AKO indicated in pink. Nineteen candidate genes were selected from the oil synthesis pathway and WGCNA results. The qRT-PCR results indicate that six key enzyme genes and three transcription factors play significant regulatory roles in AKO biosynthesis. This study elucidates the molecular pathways involved in AKO biosynthesis and explains the difference in oil content between bitter and sweet apricot kernels.
Collapse
Affiliation(s)
- Dan Zhang
- College of Forestry, Northwest A&F University, Yangling 712100, China;
| | - Zhong Zhao
- College of Forestry, Northwest A&F University, Yangling 712100, China;
- Key Laboratory of Silviculture on the Loess Plateau State Forestry Administration, Northwest A&F University, Yangling 712100, China
| |
Collapse
|
47
|
Vodrážka P, Řimnáčová L, Berková P, Vojtíšek J, Verner M, Moos M, Šimek P. A New, Validated GC-PICI-MS Method for the Quantification of 32 Lipid Fatty Acids via Base-Catalyzed Transmethylation and the Isotope-Coded Derivatization of Internal Standards. Metabolites 2025; 15:104. [PMID: 39997729 PMCID: PMC11857457 DOI: 10.3390/metabo15020104] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/09/2025] [Revised: 01/28/2025] [Accepted: 02/05/2025] [Indexed: 02/26/2025] Open
Abstract
Background: Fatty acids (FAs) represent a ubiquitous class of nonpolar alkyl carboxylate metabolites with diverse biological functions. Nutrition, metabolism, and endogenous and exogenous stress influence the overall FA metabolic status and transport via the bloodstream. FAs esterified in lipids are of particular interest, as they represent promising biomarkers of pathological diseases and nutritional status. Methods: Here, we report a validated gas chromatographic-mass spectrometric (GC-MS) method for the quantitative analysis of 32 FAs exclusively bound in esterified lipids. The developed sample preparation protocol comprises three steps using only 5 µL of human serum for Folch extraction, sodium methoxide-catalyzed transesterification in tert-butyl methyl ether, and re-extraction in isooctane prior to a quantitative GC-MS analysis with positive ion chemical ionization (PICI) and selected ion monitoring (SIM). Results: The base-catalyzed transmethylation step was studied for 14 lipid classes and was found to be efficient under mild conditions for all major esterified lipids but not for free FAs, lipid amides, or sphingolipids. To minimize matrix effects and instrument bias, internal fatty acid trideuteromethyl esters (D3-FAME) standards were prepared through isotope-coded derivatization with D3-labeled methylchloroformate/methanol medium mixed with each transmethylated serum extract for the assay. The method was validated according to FDA guidelines and evaluated by analyzing NIST SRM 2378 Serum 1 and sera from three healthy donors. Conclusions: The measured quantitative FA values are consistent with the reference data of SRM 2378, and they demonstrate the application potential of the described method for general FA analysis in esterified lipids as a novel complementary tool for lipidomics, as well as for the analysis of membrane FAs in dry blood spots and red blood cells.
Collapse
Affiliation(s)
- Petr Vodrážka
- Biology Centre, Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic; (P.V.); (L.Ř.); (P.B.)
- Department of Chemistry of Natural Compounds, University of Chemistry and Technology, Technická 5, 166 28 Prague, Czech Republic
| | - Lucie Řimnáčová
- Biology Centre, Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic; (P.V.); (L.Ř.); (P.B.)
| | - Petra Berková
- Biology Centre, Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic; (P.V.); (L.Ř.); (P.B.)
| | - Jan Vojtíšek
- Hospital České Budějovice, B. Němcové 585/54, 370 01 České Budějovice, Czech Republic; (J.V.); (M.V.)
| | - Miroslav Verner
- Hospital České Budějovice, B. Němcové 585/54, 370 01 České Budějovice, Czech Republic; (J.V.); (M.V.)
| | - Martin Moos
- Biology Centre, Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic; (P.V.); (L.Ř.); (P.B.)
| | - Petr Šimek
- Biology Centre, Czech Academy of Sciences, Branišovská 31, 370 05 České Budějovice, Czech Republic; (P.V.); (L.Ř.); (P.B.)
| |
Collapse
|
48
|
Liang X, Guo X, Yue Y, Hui F, Tong M, Guo Y, Zheng Y, Shi B, Yan S. The Effect of Increasing the Proportion of Dietary Roughage Based on the Partial Replacement of Low-Quality Roughage with Alfalfa Hay on the Fatty Acid Profile of Donkey Milk. Animals (Basel) 2025; 15:423. [PMID: 39943193 PMCID: PMC11816063 DOI: 10.3390/ani15030423] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/18/2024] [Revised: 01/24/2025] [Accepted: 01/27/2025] [Indexed: 02/16/2025] Open
Abstract
As a lactation source, donkey milk contains a higher percentage of n-3 polyunsaturated fatty acids in the milk fatty acid profile than cow's milk, especially the percentage of α-linolenic acid (ALA). We hypothesized that the ratio of dietary concentrate/roughage could influence the composition of the fatty acid (FA) profile of donkey milk, and that the substitution of low-quality roughage with high-quality roughage could improve the composition of the polyunsaturated fatty acid profile of donkey milk. The purpose of this experiment was to investigate the effects of the partial dietary replacement of low-quality roughage with alfalfa hay to increase the proportion of roughage in the diet on the FA profiles in the milk of lactating donkeys, with the goal of optimizing the FA profiles of donkey milk. The trial design was a single-factor randomized design. Sixteen Dezhou donkeys of similar age, weight, parity, and lactation days were selected and equally divided (n = 8 per group) into a low alfalfa hay group (LG, 40 concentrate/60 roughage, alfalfa hay: 44.85 g/kg dry matter) and a high alfalfa hay group (HG, 30 concentrate/70 roughage, alfalfa hay: 179.48 g/kg dry matter). The trial lasted 8 weeks and the energy and protein levels of the two diets were identical. The results showed that the profile of milk ALA increased (p = 0.048) and the n-6/n-3 ratio and index of thrombogenicity were decreased (p = 0.019 and p = 0.002) in the HG. Partial replacement of low-quality roughage with alfalfa hay and increasing the percentage of dietary roughage from 60% to 70% optimized the FA quality of donkey milk fat.
Collapse
Affiliation(s)
| | | | | | | | | | | | | | | | - Sumei Yan
- Key Laboratory of Animal Nutrition and Feed Science, College of Animal Science, Inner Mongolia Agricultural University, Universities of Inner Mongolia Autonomous Region, Hohhot 010018, China; (X.L.); (X.G.); (Y.Y.); (F.H.); (M.T.); (Y.G.); (Y.Z.); (B.S.)
| |
Collapse
|
49
|
Montenegro Gallazzi LF, Pérez CD, Rossetti L, Cunzolo S, Rizzo SA, Descalzo AM. The pasture system improves natural antioxidants and functional lipids while reducing lipid peroxidation in Ctenopharyngodon idella (grass carp) burgers during storage. Food Chem 2025; 464:141866. [PMID: 39509892 DOI: 10.1016/j.foodchem.2024.141866] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/31/2024] [Revised: 10/25/2024] [Accepted: 10/29/2024] [Indexed: 11/15/2024]
Abstract
C. idella burgers made from a pasture-based system provide a natural method for producing high-quality fish products, resulting in meat enriched with polyunsaturated fatty acids, particularly EPA and DHA, as well as fat-soluble vitamins and antioxidants. In this study, C. idella meat burgers were made from two types of diets: pasture-based (PS) and grain-based (GS). A total of 36 burgers were stored in plastic trays (three burgers per tray; 12 trays per group), in a refrigeration chamber at 4 °C ± 0.1 °C for 120 h to conduct a shelf-life experiment comparing the meats. Initial fatty acid profile and nutritional composition were determined at 0 h. Additionally, fat-soluble vitamins, antioxidants, TBA, and FRAP were measured at 0, 24, 48, 72, 96, and 120 h. PS burgers exhibited higher concentrations of n-3 LC-PUFAs, vitamins, antioxidants, except for gamma-tocopherol, and FRAP than GS burgers (P < 0.05), while GS burgers had higher TBA and γ-tocopherol (P < 0.05). Both burgers experienced vitamin reduction during storage, with PS burgers maintaining higher concentrations. Vitamin decline correlated with increased oxidation (TBA) in both burger types. These results suggest that pasture-fed burgers have longer shelf life than GS burgers due to reduced oxidation and enhanced stability of bioactive compounds.
Collapse
Affiliation(s)
- L F Montenegro Gallazzi
- Facultad de Ciencias Agrarias, Universidad Nacional de Lomas de Zamora, Buenos Aires, Argentina; Instituto de Ciencia y Tecnologia de Sistemas Alimentarios Sustentables (UEDD INTA CONICET), Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.
| | - C D Pérez
- Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina; Grupo de Investigación en Ingeniería en Alimentos (GIIA), Instituto de Ciencia y Tecnología de Alimentos y Ambiente (INCITAA), Facultad de Ingeniería, Universidad Nacional de Mar del Plata, Juan B. Justo 4302, B7600FDQ Mar del Plata, Argentina.
| | - L Rossetti
- Instituto Tecnologia de Alimentos, CIA, Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina; Instituto de Ciencia y Tecnologia de Sistemas Alimentarios Sustentables (UEDD INTA CONICET), Argentina
| | - S Cunzolo
- Instituto Tecnologia de Alimentos, CIA, Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina; Instituto de Ciencia y Tecnologia de Sistemas Alimentarios Sustentables (UEDD INTA CONICET), Argentina
| | - S A Rizzo
- Instituto Tecnologia de Alimentos, CIA, Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina; Instituto de Ciencia y Tecnologia de Sistemas Alimentarios Sustentables (UEDD INTA CONICET), Argentina
| | - A M Descalzo
- Instituto Tecnologia de Alimentos, CIA, Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Buenos Aires, Argentina; Instituto de Ciencia y Tecnologia de Sistemas Alimentarios Sustentables (UEDD INTA CONICET), Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina
| |
Collapse
|
50
|
Zhao Q, Kalpio M, Fabritius M, Zhang Y, Yang B. Analysis of triacylglycerol regioisomers in plant oils using direct inlet negative ion chemical ionization tandem mass spectrometry. Food Res Int 2025; 202:115710. [PMID: 39967165 DOI: 10.1016/j.foodres.2025.115710] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/13/2024] [Revised: 12/13/2024] [Accepted: 01/06/2025] [Indexed: 02/20/2025]
Abstract
Triacylglycerols (TGs) are the primary lipids of plant oils and the positional distribution of fatty acids (FAs) is essential to physicochemical, functional, and nutritional qualities of oils. Most studies have reported TG species in plant oils. In some studies, FA combinations in each TG species have been reported still neglecting the regioisomer composition of TGs. In this study, a fast direct inlet negative ion chemical ionization tandem mass spectrometric (NICI-MS/MS) method and optimization algorithm were applied to study the regioisomerism of TGs in 18 different plant oils. According to FA composition results, oleic, FA 18:1(9); linoleic, FA 18:2(9,12); palmitic, FA 16:0 and stearic acid, FA 18:0 were the most abundant FAs, composing mainly TG species having acyl carbon numbers 50, 52 and 54 and 1-4 double bonds. Based on 35 detected TG species, oils were classified into five groups using clustering analysis. Each group had a different dominant TG species of which the most abundant were triunsaturated ones. In regioisomeric pairs or triplets, FA 16:0, FA 16:1(9), FA 18:0, and FA 18:2(9,12) were more commonly in the sn-1/3 position, while FA 18:1 slightly preferred sn-2. The most abundant TG regioisomers were: TG 16:0_18:1(sn-2)_18:1 (52:2, mainly 18:1 in sn-2) especially in avocado, macadamia nut, olive, and palm oils; TG 18:2_18:2(sn-2)_18:1 and TG 18:2_18:1(sn-2)_18:2 (TG 54:5, mainly 18:2 in sn-2) in corn, pumpkin seed, sesame, and sunflower oils. The use of high-throughput NICI-MS/MS method to study regioisomers in commercial plant oils contributes to further studies on profiling lipid structure and developing products with specific TG compositions to meet dietary needs. The regiospecific information of TGs in edible oils is crucial for understanding their health benefits and functional properties, which are in turn needed in selecting oils for various applications.
Collapse
Affiliation(s)
- Qizhu Zhao
- Food Sciences, Department of Life Technologies, Faculty of Technology, University of Turku FI-20014 Turku, Finland
| | - Marika Kalpio
- Food Sciences, Department of Life Technologies, Faculty of Technology, University of Turku FI-20014 Turku, Finland.
| | - Mikael Fabritius
- Food Sciences, Department of Life Technologies, Faculty of Technology, University of Turku FI-20014 Turku, Finland
| | - Yuqing Zhang
- Food Sciences, Department of Life Technologies, Faculty of Technology, University of Turku FI-20014 Turku, Finland
| | - Baoru Yang
- Food Sciences, Department of Life Technologies, Faculty of Technology, University of Turku FI-20014 Turku, Finland
| |
Collapse
|