粒体自噬
糖尿病性心肌病
自噬
线粒体
心肌病
胰岛素抵抗
糖尿病
医学
线粒体生物发生
内科学
内分泌学
生物信息学
心脏病学
生物
心力衰竭
细胞生物学
遗传学
细胞凋亡
作者
Haoxiao Zheng,Hailan Zhu,Xinyue Liu,Xiaohui Huang,Anqing Huang,Yuli Huang
标识
DOI:10.3389/fcell.2021.750382
摘要
Cardiovascular disease is the leading complication of diabetes mellitus (DM), and diabetic cardiomyopathy (DCM) is a major cause of mortality in diabetic patients. Multiple pathophysiologic mechanisms, including myocardial insulin resistance, oxidative stress and inflammation, are involved in the development of DCM. Recent studies have shown that mitochondrial dysfunction makes a substantial contribution to the development of DCM. Mitophagy is a type of autophagy that takes place in dysfunctional mitochondria, and it plays a key role in mitochondrial quality control. Although the precise molecular mechanisms of mitophagy in DCM have yet to be fully clarified, recent findings imply that mitophagy improves cardiac function in the diabetic heart. However, excessive mitophagy may exacerbate myocardial damage in patients with DCM. In this review, we aim to provide a comprehensive overview of mitochondrial quality control and the dual roles of mitophagy in DCM. We also propose that a balance between mitochondrial biogenesis and mitophagy is essential for the maintenance of cellular metabolism in the diabetic heart.
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