Curcumin-attenuated trinitrobenzene sulphonic acid induces chronic colitis by inhibiting expression of cyclooxygenase-2

Abstract

AIM: To explore the possible mechanisms of curcumin in rat colitis induced by trinitrobenzene sulfonic (TNBS) acid.

METHODS: Rats with TNBS acid-induced colitis were treated with curcumin (30 mg/kg or 60 mg/kg per day ip). Changes of body weight and histological scores as well as survival rate were evaluated. Leukocyte infiltration was detected by myeloperoxidase (MPO) activity assay. The expression of cyclooxygenase-2 (COX-2) was detected by RT-PCR and Western blot. Inflammation cytokines were determined by RT-PCR. Local concentration of prostaglandin E₂ (PGE₂) in colon mucosa was determined by ELISA.

RESULTS: Curcumin improved survival rate and histological image, decreased the macroscopic scores and MPO activity. Also curcumin reduced the expression of COX-2 and inflammation cytokines. In addition, treatment with curcumin increased the PGE₂ level.

CONCLUSION: Curcumin has therapeutic effects on TNBS acid-induced colitis, the mechanisms seem to be related to COX-2 inhibition and PGE₂ improvement.

Key Words: Colitis, Curcumin, Cyclooxygenase-2, PGE₂, TNBS acid

INTRODUCTION

Inflammatory bowel disease (IBD) is characterized by chronic recurrent ulceration of the bowel. Frontline drugs that are currently used for the treatment of IBD include derivatives of 5-aminosalicvlic acid (5-ASA), glucocorticoid and immunosuppressives. Novel agents such as monoclonal antibodies against tumor necrosis factor alpha (TNF-α) are now commercially available[1,2]. However, these agents have varying efficacy and are expensive. Consequently, there is a need for alternative agents that may be equally or more effective and cheaper. Curcumin is the prominent yellow pigment in turmeric, a widely used spice and food colouring agent with anti-inflammatory and anti-cancer properties[3]. Mechanisms by which curcumin exerts its pharmacological effects are thought to involve antioxidation[4], inhibition of kinases, interference with the activity of transcription factors such as NF-κB and AP-1[5]. Cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) are inhibited by curcumin through NF-κB dependent or independent pathway[6,7].

In IBD, increased COX-2 mRNA and protein have been found in inflamed areas, and most of the PGs are produced by the COX-2 pathway. Hence, inhibition of excessive COX-2 activity and PGE₂ production may result in suppression of the inflammatory response. Preventive and therapeutic mechanisms of curcumin are to inhibit the activation of NF-κB and reduce the activity of p38 MAPK[8-11]. But whether treatment of colitis with curcumin reduces COX-2 and PGE₂ remains unknown. In the present study, we investigated the effect of curcumin on body weight changes, the expression of COX-2, the local concentration of PGE₂ in colon mucosa and the changes of inflammatory genes in rats with colitis induced by trinitrobenzene sulphonic (TNBS) acid.

MATERIALS AND METHODS

Experimental animals

Specific pathogen-free Sprague-Dawley rats weighing 200-220 g were obtained from Laboratory Animal Center of Wuhan University (Wuhan, China) and kept at constant temperature (23 ± 2°C) and humidity (50%-70%) in a 12 h light and dark cycle. The rats were allowed to adapt to our laboratory environment for one week before experiment with free access to standard rodent chow and tap water.

Induction of colitis

Colitis was induced by TNBS acid using the modified method described by Morris et al[12]. Briefly, rats were fasted the day before colitis induction. Each rat was anesthetized with ether, and 100 mg/kg of TNBS acid (Sigma, St. Louis, MO, 100 g/L TNBS acid in 500 mL/L ethanol, total volume 1.0 mL) was then instilled via a rubber catheter inserted 8 cm into the colon via the anus. The rubber catheter was modified with numerous holes in the last 4 cm of its length. The instillation procedure required only a few seconds and the rats were maintained in a vertical position for 3 min to prevent solution leakage. Control mice received 500 mL/L ethanol of the same volume using the same technique. All the rats were checked daily for behavior and body mass. The experiments were approved by the Institution’s Animal Care and Use Committee.

Treatment protocols

To investigate the therapeutic and dosage effects of curcumin(≥ 95%, Sigma), rats were randomly divided into four groups: control group(n = 15, receiving ethanol only and no treatment), TNBS acid group(n = 15, receiving TNBS acid and no treatment), curL group(n = 15, receiving 30 mg/kg curcumin per day ip) and curH group(n = 15, receiving curcumin 60 mg/kg per day ip). On d 1, the rats were fasted, colitis was induced and treatment was begun on d 2. Con and TNBS acid groups received the same volume of 5% ethanol (vehicle of curcumin) everyday until the end of the experiment. Treated groups received curcumin just after colitis was induced for two weeks until the rats were sacrificed.

Assessment of severity of colitis

After rapid removal of the colon, specimens were flushed with ice cold PBS, cut open and photographed. The photographs of the colonic specimens were then scored by a blinded observer unaware of the treatment. Scores were assessed by using the following damage scoring system[12]: 0: no damage; 1: localized hyperaemia without ulcers; 2: linear ulcers with no significant inflammation; 3: linear ulcer with inflammation at one site; 4: two or more sites of ulceration and/or inflammation; 5: two or more major sites of inflammation and ulceration or one major site of inflammation and ulceration extending more than 1 cm along the colon. For histological analysis, tissues were fixed in 100 g/L paraformaldehyde in phosphate-buffered saline, and paraffin-embedded tissue sections were stained with hematoxylin and eosin (HE) using the standard techniques.

Assessment of leukocyte infiltration

Myeloperoxidase (MPO) activity was assessed as a marker of neutrophil infiltration. Rat colon samples were snap-frozen in liquid nitrogen and stored at -80°C before MPO activity assessment. The tissue was thawed, weighed and homogenized in PBS, the homogenate was centrifuged and the pellet was again homogenized in PBS containing 5 g/L hexadecyl-trimethylammonium bromide (HETAB) and 10 mmol/L EDTA. This homogenate was subjected to three cycles of freezing/thawing and brief sonication. A sample of homogenates was added to reaction volume (containing 80 mmol/L PBS, pH 5.4, 5 g/L HETAB and 1.6 mmol/L 3, 3’, 5, 5’-tetramethylbenzidine). The mixture was incubated at 37°C for 5 min and the reaction was started by the addition of H₂O₂. The complete reaction mixture was incubated for exactly 3 min at 37°C and terminated by the sequential addition of catalase and sodium acetate. The changes in absorbance at 655 nm were measured with a spectrophotometer.

Semi-quantitative RT-PCR

For RT-PCR, rat colon samples were snap-frozen in liquid nitrogen and stored at -80°C before ribonucleic acid (RNA) preparation. Total RNA was isolated using the TRIzol method (Life Technologies, Canada). Concentration of the RNA was detected from A₂₆₀, and the integrity of the RNA was verified by electrophoresis on formaldehyde gels. Total RNA was reverse-transcribed into complementary deoxyribonucleic acids (cDNAs) using a first strand cDNA synthesis kit (Fermentas, Life Sciences).The resultant cDNAs were subjected to PCR for measurement of messenger RNAs (mRNAs). The PCR products were subjected to agarose gel electrophoresis and the abundance of each mRNA was normalized to that of GAPDH. The sequences of all primers used in this project are as flowing:

GAPDH: sense: 5’ATGGGTGTGAACCACGAGAAA-3’,

anti-sense: 5’GGATACATTGGGGGTAGG-AA-3’(330 bp);

COX-2: sense: 5’-TACAAGCAGTGGCAAAGGC-3’,

anti-sense: 5’-CAGTATTGAGGAGAACAGATGGG-3’(304 bp);

TNF-α: sense: 5’-TACTGAACTTCGGGGTGATTGGTCC-3’,

anti-sense: 5’-CAGCCTTGTCCCTTGAAGAGAACC-3’(295 bp);

IFN- sense:5’AGCCTAGAAAGTCTGAAGAAC-3’,

anti-sense:5’ACCGACTCCTTTTCCGCTTC-CT-3’(387 bp)

iNOS: sense:5’-TGAAGCACATGCAGAAATGAGTACCG-3’,

anti-sense: 5’-CCGTCAGAGGTAACTGTTTACACG-3’ (464 bp)

Western blot analysis

Western blot analysis was performed by standard methods. Briefly, frozen tissue samples were homogenized in Tris-HCl buffer containing a cocktail of protease inhibitors and insoluble materials removed by centrifugation at 4°C. The solubilized lysates were resolved by sodium dodecyl sulfate (SDS)-PAGE electrophoresis under reducing conditions at a concentration of 50 μg protein of each sample per lane. Nitrocellulose membranes were incubated overnight with rabbit anti-serum directed against COX-2 (Santa Cruz Biotechnology). Immunodetection with secondary peroxidase-conjugated antibody and chemiluminescence was performed according to the manufacturer’s protocol (Santa Cruz Biotechnology). Density of the products was quantified.

Enzyme-link immunosorbent analysis

Colonic mucosal samples kept at -80°C were weighed and homogenized on ice in 1 mL Tris-HCl buffer containing 5.6 mmol/L indomethacin (pH 7.4), the homogenization was vortexed thoroughly for at least 2 min. After centrifugation, the concentration of PGE₂ in supernatants was immediately determined with competitive ELISA kits (R&D), according to the manufacturer’s instructions. PGE₂ levels were normalized to microgram of protein. The detection limit of PGE₂ was 39 ng/L.

Statistical analysis

Data were expressed as mean ± SE. The statistical significance was evaluated by one-way analysis of variance (ANOVA) followed by Dunnett’s test. P < 0.05 was considered statistically significant. In the experiment involving histology, the figures shown are representative of at least three experiments performed on different days.

RESULTS

Body mass

Administration of TNBS acid caused a dramatically decrease in body mass of all groups. Most of them decreased more than 30 g after 2 d (data not shown). Con group showed transient and slight loss of body weight (less than 10 g, data not shown) and recovered quickly. From d 3 it began to show significant difference from TNBS acid group (P < 0.05, Figure 1). At the end of the experiment, except for TNBS acid group, body weight of the other groups all reached the initial level. No difference was observed among control, curL and curH groups at the end of the experiment.

Figure 1 Body mass changes in rats with TNBS acid-induced colitis. Each bar represents mean ± SE. P < 0.05 vs TNBS acid.

Macroscopic scores and histological images

TNBS acid-induced colitis was characterized by thick and stiff colonic wall due to edema, chemical erosion or fibriform-proliferation. Ulcers were scattered along the colon or linked with each other, bleeding or redness was observed in whole or partial colon. Necrosis of epithelium, distortion of crypts, destruction of glands and infiltration of inflammatory cells were observed. The macroscopic scores in curL and curH groups were significantly lower than those in TNBS acid group (P < 0.01 Figure 2). Treatment with curcumin decreased edema. Ulcers in curcumin-treated groups were much smaller and superficial, most of the ulcers were healed and granulation or fibroplasias could be seen. Histological analysis showed that curcumin treatment decreased necrosis of epithelium and the infiltration of inflammatory cells and granulation can be seen.

Figure 2 Effects of curcumin on histological scores of rats with TNBS acid-induced colitis in control group (A), TNBS acid group (B), and cur group (C). (HE staining, original magnification: × 200).

Leukocyte involvements

Myeloperoxidase activity was significantly (P < 0.01) increased in TNBS acid-treated animals compared with control group (101 020 ± 17 170 nkat/g and 249 382 ±43 342 nkat/g tissue protein, respectively, Table 1 ), which was consistent with the histological findings. Treatment with curcumin (30 mg/kg or 60 mg/kg per day) significantly reduced the degree of polymorphonuclear and neutrophil infiltration in rats with TNBS acid-induced colitis.

Table 1 Concentrations of PGE₂ , activities of MPO in colon tissue and mRNA in inflammatory response genes (mean ± SE).

	Tissue PGE2 (ng/g)	Protein MPO (knat/g)	TNF-α	mRNA IFN-γ	iNOS
Con 15	176.3 ± 29.2c	101 020 ± 17 170d	0.0795 ± 0.0096d	0.0284 ± 0.0150d	0.8304 ± 0.1180d
TNBS 8	78.5 ± 13.2a	249 382 ± 43 342b	0.8861 ± 0.0533b	1.0212 ± 0.0687b	6.5690 ± 0.9450b
CurL 12	190.2 ± 17.0c	121 691 ± 23 171ad	0.1967 ± 0.0365bd	0.0565 ± 0.0177ad	1.8638 ± 0.3347bd
CurH 13	215.5 ± 20.4ac	122 191 ± 21 171ad	0.1727 ± 0.0348bd	0.0518 ± 0.0057d	1.7250 ± 0.3026bd

^aP < 0.05, ^bP < 0.01 vs control; ^cP < 0.05, ^dP < 0.01 vs TNBS acid (Dunnett’s t test)

COX-2 and PGE₂ expression

Weak expression of COX-2 mRNA could be detected in normal colon (Figure 3). After colitis was induced by TNBS acid, its expression increased by more than 10-fold. Treatment with curcumin decreased its expression by 70%, but was still higher than normal (P < 0.05). Western blot analysis showed the similar changes of protein in colon mucosa (Figure 3). After colitis was induced, PGE₂ decreased and its expression was increased after curcumin treatment.

Figure 3 COX-2 expression in rats with TNBS acid-induced colitis. A: COX-2 mRNA; B: COX-2 products; C and D: COX-2 protein (M_r72 000) (mean ± SE, Dunnett’s t test). ^bP < 0.01 vs control; ^dP < 0.01 vs TNBS acid.

Expression of inflammatory mediator genes

Abundance of IFN-γ, TNF-α and iNOS mRNA in TNBS acid group was significantly elevated compared with control group. Curcumin treatment suppressed the increased mRNA efficiently, but its level was still higher than normal (Table 1).

DISCUSSION

Treatment with curcumin (30 mg/kg or 60 mg/kg per day) reduced the severity and extension of damage induced by TNBS acid, decreased the extent of colitis and increased the survival rate and the incidence of adhesions. The rats treated with curcumin had improved histological image and less neutrophil infiltration in colon mucosa. The expression of COX-2 increased in acute and chronic colitis, suggesting that over-expression of COX-2 may result in neoplasia[13-17]. Curcumin exerts its antitumor and anti-inflammation effects by down-regulating COX-2 directly or indirectly[18]. Some reports indicate that selective COX-2 inhibitors exacerbate colitis[19-21], but others indicate that they have therapeutic effects on colitis[22-26]. In our experiment, the expression of COX-2 increased in colon following the induction of colitis, suggesting that high expression of COX-2 in the colon is associated with high MPO activity and cytokine production. Curcumin decreased the level of COX-2, indicating that decreasing the expression of COX-2 may benefit to colitis.

PGE₂, an inflammatory mediator, participates in epithelium repairing and exerts anti-inflammation effects including suppression of neutrophil function or prevention of mast cell degranulation. Recently, PGE₂ has been implicated in the inhibition of the production of IFN-γ, IL-2 and IL-12[27]. It was reported that in early or acute inflammation phase the expression of PGE₂ is usually up-regulated, resulting in inflammatory manifestations, such as redness, edema, pyrexia and ache[15,28]. Treatment with curcumin increased the expression of PGE₂ though its limiting enzyme COX-2 decreased, indicating that curcumin can change the expression spectrum of PGs in colitis.

TNBS acid-induced chronic intestinal inflammation mimics human Crohn’s disease, showing high IFN-γ, TNF-α and iNOS, but low levels of IL-4 and IL-5[19,29]. Treatment with curcumin decreased IFN-γ, TNF-α and iNOS distinctly in our study, which is consistent with the reports of Ukil et al[11] and Sugimoto et al[9]. Since PGE₂ is capable of inhibiting Th1 cytokines, the decreased IFN-γ, TNF-α and iNOS in this study maybe due to PGE₂. Although curcumin decreased the expression of inflammatory response genes, but not decrease it to the normal level, suggesting that curcumin is not able to completely eliminate colitis.

Curcumin (30 mg/kg or 60 mg/kg per day) did not show any difference in the treatment of colitis induced by TNBS acid. Curcumin is also a chemopreventive drug for many tumors[18]. IBD patients are at risk of developing dysplasia and neoplasia. Phase I clinical trial of curcumin indicated that 8 g/d for 3 mo does not show any toxicity[30], suggesting that long-term administration of curcumin in IBD patients is not only safe but also improves colitis and prevents development of colorectal cancer.

In conclusion, curcumin attenuates TNBS acid-induced chronic colitis by decreasing the expression of COX-2 and increasing PGE₂. Curcumin can down regulate the expression of inflammatory genes in colitis induced by TNBS acid and is a safe and therapeutic agent for IBD patients