Pioglitazone Induces Cardiomyocyte Apoptosis and Inhibits Cardiomyocyte Hypertrophy Via VEGFR-2 Signaling Pathway

• Published in: Arquivos brasileiros de cardiologia 2018-08, Vol.111 (2), p.162-169
• Main Authors: Zhong, Wenliang, Jin, Wen, Xu, Shanghua, Wu, Yanqing, Luo, Shunxiang, Liang, Minlie, Chen, Lianglong
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; Anti-Hipertensivos; Apoptose; Apoptosis - drug effects; CARDIAC & CARDIOVASCULAR SYSTEMS; Cardiomegalia; Hypertrophy - chemically induced; Hypertrophy - pathology; Hypoglycemic Agents - pharmacology; Insuficiência Cardíaca/fisiopatologia; Miócitos Cardíaco; Myocytes, Cardiac - drug effects; Myocytes, Cardiac - pathology; Original; Rats; Rats, Sprague-Dawley; Resistência à Insulina; Signal Transduction - drug effects; Thiazolidinediones - pharmacology; Tiazolidinedionas; Vascular Endothelial Growth Factor Receptor-2 - drug effects
• ISSN: 0066-782X; 1678-4170; 1678-4170
• DOI: 10.5935/abc.20180108

Pioglitazone has been widely used as an insulin-sensitizing agent for improving glycemic control in patients with type 2 diabetes mellitus. However, cardiovascular risk and protective effects of pioglitazone remain controversial. In this study, we investigated whether pioglitazone affects cardiomyocyte apoptosis and hypertrophy by regulating the VEGFR-2 signaling pathway. Cardiomyocytes were enzymatically isolated from 1- to 3-day-old Sprague-Dawley rat ventricles. Effects of pioglitazone and the VEGFR-2-selective inhibitor apatinib on cardiomyocyte apoptotic rate was determined using flow cytometry, and hypertrophy was evaluated using [3H]-leucine incorporation. The protein expressions of unphosphorylated and phosphorylated VEGFR-2, Akt, P53, and mTOR were determined by Western-Blotting. Analysis of variance (ANOVA) was used to assess the differences between groups. Pioglitazone and VEGFR-2-selective inhibitor apatinib reduced rat cardiomyocyte viability and cardiomyocyte hypertrophy induced by angiotensin II in vitro. Furthermore, in the same in vitro model, pioglitazone and apatinib significantly increased the expression of Bax and phosphorylated P53 and decreased the expression of phosphorylated VEGFR-2, Akt, and mTOR, which promote cardiomyocyte hypertrophy. These findings indicate that pioglitazone induces cardiomyocyte apoptosis and inhibits cardiomyocyte hypertrophy by modulating the VEGFR-2 signaling pathway.