Jinxinkang granule alleviates chronic heart failure by enhancing GPER/AMPK/PCG-1α-mediated fatty acid oxidation

Haixiang Zhong , Liu He , Wanru Zhong , Lili Wang , Jianmin Luo , Qi Chen , Rong Li , Rong Zhang , Zhongqiu Liu , Yuanyuan Cheng
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Abstract

Introduction

Chronic heart failure (CHF) is considered to be the last battlefield of cardiovascular disease. Jinxinkang granule (JXK) is an integrated traditional Chinese medicine formula for treating CHF. Our previous clinical study showed that JXK could increase the left ventricular ejection fraction and reduce concomitant symptoms in patients with CHF. However, the molecular mechanism underlying the action of JXK on CHF has yet to be fully illustrated.

Methods

Sprague-Dawley (SD) rats under left anterior descending artery ligation model, C57BL/6 mice subcutaneously injected isoproterenol (ISO) model in vivo and H9c2 cells under oxygen glucose deprivation (OGD) in vitro were used to evaluate the effect of JXK against CHF. Cardiac function and morphology assessment using M-mode echocardiography, H&E/Masson/WGA staining, western blotting analysis, real-time PCR detection, ATP and cAMP assays were used to explore the mechanism of JXK against CHF.

Results

JXK improved cardiac function and ameliorated cardiac fibrosis in both LAD-induced CHF rats and ISO-induced CHF mice, and protected cardiomyocytes from OGD injury in H9c2 cells. Moreover, JXK increased the level of ATP content and enhanced fatty acid oxidation by increasing CD36, CPT1A and ACADM expression. Mechanism study showed that JXK increased the GPER expression and cAMP level, promoted AMPK phosphorylation and PGC-1α expression. Additionally, molecular docking analysis showed that dihydroisotanshinone I has a high binding affinity with GPER at -8.5 kcal/mol, which has the similar binding sites with G-1, a GPER agonist. Importantly, after using the inhibitor of GPER (G15), the cardioprotective effect of JXK and the enhancing effect on the fatty acid oxidation were blocked.

Conclusion

JXK effectively activated GPER/AMPK/PGC-1α signaling pathway to enhance the oxidation of fatty acid, thereby promoting cardiac energy metabolism production to ameliorate CHF.

Abstract Image

金心康颗粒通过增强GPER/AMPK/ pcg -1α-介导的脂肪酸氧化而缓解慢性心力衰竭
慢性心力衰竭(CHF)被认为是心血管疾病的最后战场。金心康颗粒是治疗慢性心力衰竭的中西医结合方剂。我们之前的临床研究表明,JXK可以提高CHF患者的左心室射血分数,减少伴随症状。然而,JXK对CHF作用的分子机制尚未完全阐明。方法采用SD大鼠左前降支结扎模型,C57BL/6小鼠皮下注射异丙肾上腺素(ISO)模型,体外氧糖剥夺(OGD) H9c2细胞,观察JXK对CHF的作用。采用m型超声心动图、H&;E/Masson/WGA染色、western blotting分析、real-time PCR检测、ATP和cAMP检测等方法评估心功能和形态学,探讨JXK抗CHF的作用机制。结果jxk可改善ladd诱导的CHF大鼠和iso诱导的CHF小鼠的心功能和心肌纤维化,并可保护H9c2细胞免受OGD损伤。此外,JXK通过增加CD36、CPT1A和ACADM的表达,提高ATP含量,促进脂肪酸氧化。机制研究表明,JXK增加GPER表达和cAMP水平,促进AMPK磷酸化和PGC-1α表达。此外,分子对接分析表明,二氢异丹参酮I与GPER具有-8.5 kcal/mol的高结合亲和力,与GPER激动剂G-1具有相似的结合位点。重要的是,在使用GPER抑制剂(G15)后,JXK的心脏保护作用和脂肪酸氧化增强作用被阻断。结论jxk有效激活GPER/AMPK/PGC-1α信号通路,增强脂肪酸氧化,从而促进心脏能量代谢产生,改善CHF。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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