医学
败血症
心肌病
发病机制
机制(生物学)
GPX4
感染性休克
并发症
重症监护医学
免疫学
内科学
心力衰竭
氧化应激
谷胱甘肽过氧化物酶
哲学
过氧化氢酶
认识论
作者
Jiayu Song,Yiming He,Kaixuan Zhou,Jiabao Xue,Zi Xue,Lijing Li
出处
期刊:PubMed
日期:2022-10-01
卷期号:34 (10): 1107-1111
被引量:2
标识
DOI:10.3760/cma.j.cn121430-20220823-00776
摘要
Sepsis is a serious complication of infection, and its further development may lead to multi-organ dysfunction syndrome. Sepsis cardiomyopathy is a common complication of sepsis and has been directly linked to high mortality. Although the pathogenesis of septic cardiomyopathy is not fully understood, in-depth study of the pathogenesis of septic cardiomyopathy and the identification of its potential therapeutic targets may reduce mortality in patients with sepsis. Ferroptosis is an iron-dependent mode of cell death that has been shown to be involved in the pathophysiological mechanisms of many diseases. Some related studies have reported that ferroptosis may be a potential mechanism of septic cardiomyopathy. This review provides new insights into the mechanisms of mitochondrial dysfunction, lipid peroxidation, xc-system, glutathione peroxidase 4 (GPX4), iron metabolism and the role of ferroptosiswith septic cardiomyopathy for further research and treatment of septic cardiomyopathy.
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