©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 9 Farrerol alleviates high glucose and free fatty acid-induced endothelial cell dysfunction via inhibition of miR-29b-3p.
A and B: Representative immunofluorescence images and quantitative analysis of the intensity endothelial anchoring junctions (VE-cadherin). Bar = 100 μm. n = 6; C and D: Representative images of immunofluorescence staining of intercellular adhesion molecule-1 (VCAM-1) and quantitative analysis of VCAM-1 intensity. Bar = 20 μm. n = 6; E-G: Western blots analysis and quantitative data of VCAM-1 and endothelial nitric oxide synthase expression in high glucose and free fatty acid treated endothelial cells (n = 3). aP < 0.05 vs NC; bP < 0.05 vs HG/FFA + mimic NC; cP < 0.05 vs HG/FFA + miR-29b-3p mimic; dP < 0.05 vs HG/FFA + FA + mimic NC. eNOS: Endothelial nitric oxide synthase; ICAM-1: Intercellular adhesion molecule-1; HG/FFA: High glucose and free fatty acid; FA: Farrerol.
- 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