Suppr超能文献

辛伐他汀通过诱导自噬来保护高糖诱导的 H9c2 细胞免受损伤。

Simvastatin protects high glucose-induced H9c2 cells from injury by inducing autophagy.

机构信息

Department of Cardiology, Inner Mongolia People's Hospital, Hohhot, China.

Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Pharm Biol. 2020 Dec;58(1):1077-1084. doi: 10.1080/13880209.2020.1839512.

Abstract

CONTEXT

Simvastatin is the first line therapeutic drug for coronary heart disease and atherosclerosis. The protective effect mechanism of simvastatin on cardiomyocytes is unclear.

OBJECTIVE

This study explores the effect of simvastatin on high glucose induced cardiomyocyte injury and the role of autophagy during the process.

MATERIALS AND METHODS

H9c2 cells were incubated with different doses of glucose (0, 50, 100, 200 mM) for 24 h to verify the glucose induced injury. The H9c2 cells were pre-treated with simvastatin at different dosages (0, 0.1, 0.5, 1 μM) for 30 min to rescue the injury followed by the autophagy evaluation. 3-MA was used as an autophagy inhibitor to confirm the role of autophagy in simvastatin treated process. CCK-8 assay, FACS assay, confocal microscopy, western blotting and immunofluorescence analysis were conducted to evaluate the high glucose induced injury or protective effects of simvastatin in H9c2 cell line.

RESULTS

High glucose dramatically decreased H9c2 cell viability (0 mM, 0.58 ± 0.09%; vs. 50 mM, 8.67 ± 0.43%; 100 mM, 16.1 ± 3.56%; 200 mM, 32.9 ± 2.63%), induced significant cell apoptosis (0 mM, 0.96 ± 0.16%, vs. 50 mM, 7.00 ± 0.63%; 100 mM, 12.9 ± 0.78%; 200 mM, 21.8 ± 1.17%) and suppressed cell autophagy. Simvastatin decreased apoptosis and attenuate injury by decreasing cell apoptosis ratio, elevating Bcl-2 expression while decreasing Bax and caspase-3 protein expressions. Meanwhile, simvastatin restored the autophagy depicted by western blotting with increased ATG-5, Beclin1 and LC3II/LC3I protein expression and decreased p62 expression, as well as immunofluorescence with elevated LC3 fluorescence density.

DISCUSSION AND CONCLUSIONS

The myocardial protective effect mediated by autophagy activated by simvastatin to some extent elucidated the mechanism of the protective effect of simvastatin on H9c2 cell injury, which provided a certain theoretical basis for the clinical application of simvastatin in the treatment of cardiovascular diseases. In addition, we speculate that simvastatin may be used for diabetes associated cardiovascular diseases.

摘要

背景

辛伐他汀是治疗冠心病和动脉粥样硬化的一线治疗药物。辛伐他汀对心肌细胞的保护作用机制尚不清楚。

目的

本研究探讨了辛伐他汀对高糖诱导的心肌细胞损伤的作用及其在该过程中自噬的作用。

材料和方法

用不同浓度的葡萄糖(0、50、100、200 mM)孵育 H9c2 细胞 24 h 验证葡萄糖诱导的损伤。用不同剂量的辛伐他汀(0、0.1、0.5、1 μM)预处理 H9c2 细胞 30 min 以挽救损伤,然后评估自噬。用 3-MA 作为自噬抑制剂来确认自噬在辛伐他汀处理过程中的作用。CCK-8 测定、FACS 分析、共聚焦显微镜、western blot 和免疫荧光分析用于评估 H9c2 细胞系中高葡萄糖诱导的损伤或辛伐他汀的保护作用。

结果

高葡萄糖显著降低 H9c2 细胞活力(0 mM,0.58±0.09%;50 mM,8.67±0.43%;100 mM,16.1±3.56%;200 mM,32.9±2.63%),诱导显著的细胞凋亡(0 mM,0.96±0.16%;50 mM,7.00±0.63%;100 mM,12.9±0.78%;200 mM,21.8±1.17%)和抑制细胞自噬。辛伐他汀通过降低细胞凋亡率、增加 Bcl-2 表达、降低 Bax 和 caspase-3 蛋白表达,减少细胞凋亡,减轻损伤。同时,辛伐他汀通过增加 ATG-5、Beclin1 和 LC3II/LC3I 蛋白表达,降低 p62 表达,Western blot 和免疫荧光显示自噬恢复,LC3 荧光密度增加。

讨论和结论

辛伐他汀通过激活自噬介导的心肌保护作用在一定程度上阐明了辛伐他汀对 H9c2 细胞损伤保护作用的机制,为辛伐他汀在心血管疾病治疗中的临床应用提供了一定的理论依据。此外,我们推测辛伐他汀可能用于糖尿病相关的心血管疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf23/7655079/03a25f8c41c4/IPHB_A_1839512_F0001_C.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验