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©The Author(s) 2025.
World J Diabetes. Jun 15, 2025; 16(6): 103685
Published online Jun 15, 2025. doi: 10.4239/wjd.v16.i6.103685
Published online Jun 15, 2025. doi: 10.4239/wjd.v16.i6.103685
Figure 9 Inhibition of nuclear factor erythroid 2-related factor 2 reverses the effect of erianin on type 2 diabetes mellitus mice.
A: Hematoxylin-eosin-stained myocardial section; B: Markers of myocardial damage; C: Serum proinflammatory factors; D: mRNA levels of proinflammatory factors; E: Oxidative stress. Bar charts represent the mean ± SEM, n = 8. aP < 0.05 vs control group; bP < 0.01 vs control group; cP < 0.001 vs control group; dP < 0.05 vs model group; eP < 0.01 vs model group; fP < 0.001 vs model group; CK: Creatine kinase; CK-MB: Creatine kinase-isoenzymes; cThI: Cardiac troponin I; TNF-α: Tumor necrosis factor-α; IL: Interleukin; MDA: Malondialdehyde; SOD: Superoxide dismutase; CAT: Catalase.
- Citation: Chen JH, Dai XC, Quan ZJ, Liu XY. Erianin mitigates diabetic cardiomyopathy via adenosine monophosphate-activated protein kinase-nuclear factor erythroid 2-related factor 2-heme oxygenase-1 pathway activation. World J Diabetes 2025; 16(6): 103685
- URL: https://www.wjgnet.com/1948-9358/full/v16/i6/103685.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i6.103685