©The Author(s) 2025.
World J Diabetes. Sep 15, 2025; 16(9): 109553
Published online Sep 15, 2025. doi: 10.4239/wjd.v16.i9.109553
Published online Sep 15, 2025. doi: 10.4239/wjd.v16.i9.109553
Figure 7 The effects of upregulation or downregulation of miR-29b-3p on cardiac microvascular injury in diabetic cardiomyopathy mice.
A and B: Cardiac microvascular density was determined using CD31-positive endothelial cells, and large vessels were excluded (n = 6); C: Perivascular leakage of albumin was detected by immunofluorescence staining and quantified. Bar = 50 μm; D-G: Protein expression of intercellular adhesion molecule-1, VE-cadherin and endothelial nitric oxide synthase were detected by western blot and quantified (n = 3). aP < 0.05 vs NC; bP < 0.05 vs DCM. DCM: Diabetic cardiomyopathy; ECs: Endothelial cells; ICAM-1: Intercellular adhesion molecule-1; eNOS: Endothelial nitric oxide synthase.
- Citation: Guo Y, Yu XR, Gu HD, Wang YJ, Yang ZG, Chi JF, Zhang LP, Lin H. Farrerol ameliorates diabetic cardiomyopathy by inhibiting ferroptosis via miR-29b-3p/SIRT1 signaling pathway in endothelial cells. World J Diabetes 2025; 16(9): 109553
- URL: https://www.wjgnet.com/1948-9358/full/v16/i9/109553.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i9.109553