Mitochondrial Quality Control Mechanisms during Diabetic Cardiomyopathy

被引:15
|
作者
Ketenci, Melis [1 ]
Zablocki, Daniela [1 ]
Sadoshima, Junichi [1 ]
机构
[1] Rutgers Biomed & Hlth Sci, Rutgers New Jersey Med Sch, Dept Cell Biol & Mol Med, Newark, NJ 07107 USA
来源
JMA JOURNAL | 2022年 / 5卷 / 04期
关键词
Mitophagy; Autophagy; Diabetic Cardiomyopathy; Mitochondria; Diabetes Mellitus; Heart Failure; HEART-FAILURE; CELL-DEATH; PINK1/PARKIN-MEDIATED MITOPHAGY; AUTOPHAGY; INJURY; DRP1; PROTECTS; EMPAGLIFLOZIN; INFLAMMATION; DYSFUNCTION;
D O I
10.31662/jmaj.2022-0155
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One of the major complications of diabetes mellitus is diabetic cardiomyopathy. One of the mechanisms that initiates the irreversible deterioration of cardiac function in diabetic cardiomyopathy is mitochondrial dysfunction. Functionally impaired mitochondria result in greater levels of oxidative stress and lipotoxicity, both of which exacerbate mitochondrial damage. Mitochondrial health is constantly monitored by mitochondrial quality control mechanisms. Mitophagy selectively degrades damaged mitochondria, thereby maintaining the healthy pool of mitochondria and preserving myocardial function. Mitophagy in diabetic cardiomyopathy is mediated by multiple mechanisms in a time-dependent manner. Potential targets for the treatment of diabetic cardiomyopathy include increased oxidative stress, mitochondrial dynamics, and mitochondrial clearance. Thus, stimulation of mitophagy represents a promising strategy for the alleviation of diabetic cardiomyopathy.
引用
收藏
页码:407 / 415
页数:9
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