糖尿病性心肌病
GPX4
糖尿病
医学
心肌病
血糖性
程序性细胞死亡
心力衰竭
脂质过氧化
内科学
死因
心脏病学
氧化应激
谷胱甘肽过氧化物酶
细胞凋亡
内分泌学
超氧化物歧化酶
疾病
化学
生物化学
作者
Flobater Gawargi,Paras Kumar Mishra
出处
期刊:American Journal of Physiology-regulatory Integrative and Comparative Physiology
[American Physiological Society]
日期:2023-12-01
卷期号:325 (6): R665-R681
标识
DOI:10.1152/ajpregu.00117.2023
摘要
Ferroptosis is a newly identified myocardial cell death mechanism driven by iron-dependent lipid peroxidation. The presence of elevated intramyocardial lipid levels and excessive iron in patients with diabetes suggest a predominant role of ferroptosis in diabetic cardiomyopathy. As myocardial cell death is a precursor of heart failure, and intensive glycemic control cannot abate the increased risk of heart failure in patients with diabetes, targeting myocardial cell death via ferroptosis is a promising therapeutic avenue to prevent and/or treat diabetic cardiomyopathy. This review provides updated and comprehensive molecular mechanisms underpinning ferroptosis, clarifies several misconceptions about ferroptosis, emphasizes the importance of ferroptosis in diabetes-induced myocardial cell death, and offers valuable approaches to evaluate and target ferroptosis in the diabetic heart. Furthermore, basic concepts and ideas presented in this review, including glutathione peroxidase-4-independent and mitochondrial mechanisms of ferroptosis, are also important for investigating ferroptosis in other diabetic organs, as well as nondiabetic and metabolically compromised hearts.
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