Department of Pharmacology, School of Basic Medical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing 100191, China.
State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University, Beijing 100191, China.
Int J Mol Sci. 2024 Sep 25;25(19):10297. doi: 10.3390/ijms251910297.
Cardiac remodeling, a critical process that can lead to heart failure, is primarily characterized by cardiac hypertrophy. Studies have shown that transgenic mice with Gαq receptor blockade exhibit reduced hypertrophy under induced pressure overload. GQ262, a novel Gαq/11 inhibitor, has demonstrated good biocompatibility and specific inhibitory effects on Gαq/11 compared to other inhibitors. However, its role in cardiac remodeling remains unclear. This study aims to explore the anti-cardiac remodeling effects and mechanisms of GQ262 both in vitro and in vivo, providing data and theoretical support for its potential use in treating cardiac remodeling diseases. Cardiac hypertrophy was induced in mice via transverse aortic constriction (TAC) for 4 weeks and in H9C2 cells through phenylephrine (PE) induction, confirmed with WGA and H&E staining. We found that GQ262 improved cardiac function, inhibited the protein and mRNA expression of hypertrophy markers, and reduced the levels of apoptosis and fibrosis. Furthermore, GQ262 inhibited the Akt/mTOR signaling pathway activation induced by TAC or PE, with its therapeutic effects disappearing upon the addition of the Akt inhibitor ARQ092. These findings reveal that GQ262 inhibits cardiomyocyte hypertrophy and apoptosis through the Akt/mTOR signaling pathway, thereby reducing fibrosis levels and mitigating cardiac remodeling.
心脏重构是一种导致心力衰竭的关键过程,其主要特征是心肌肥厚。研究表明,在诱导的压力超负荷下,Gαq 受体阻断的转基因小鼠表现出心肌肥厚减少。与其他抑制剂相比,新型 Gαq/11 抑制剂 GQ262 具有良好的生物相容性和对 Gαq/11 的特异性抑制作用。然而,其在心脏重构中的作用尚不清楚。本研究旨在探讨 GQ262 在体内外的抗心脏重构作用及其机制,为其在治疗心脏重构疾病中的潜在应用提供数据和理论支持。通过横主动脉缩窄(TAC)诱导小鼠 4 周和通过苯肾上腺素(PE)诱导 H9C2 细胞,用 WGA 和 H&E 染色证实诱导出心肌肥厚。我们发现 GQ262 改善了心脏功能,抑制了肥大标志物的蛋白和 mRNA 表达,降低了细胞凋亡和纤维化水平。此外,GQ262 抑制了 TAC 或 PE 诱导的 Akt/mTOR 信号通路激活,加入 Akt 抑制剂 ARQ092 后其治疗效果消失。这些发现表明,GQ262 通过 Akt/mTOR 信号通路抑制心肌细胞肥大和凋亡,从而降低纤维化水平并减轻心脏重构。