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铁死亡在心血管疾病中的分子机制。

Molecular mechanisms of ferroptosis in cardiovascular disease.

机构信息

Department of Biochemistry and Molecular Biology, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.

The Affiliated Nanhua Hospital, Department of Clinical Laboratory, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.

出版信息

Mol Cell Biochem. 2024 Dec;479(12):3181-3193. doi: 10.1007/s11010-024-04940-2. Epub 2024 Feb 19.

Abstract

Ferroptosis is a newly recognized type of regulated cell death that is characterized by the accumulation of iron and lipid peroxides in cells. Studies have shown that ferroptosis plays a significant role in the pathogenesis of various diseases, including cardiovascular diseases. In cardiovascular disease, ferroptosis is associated with ischemia-reperfusion injury, myocardial infarction, heart failure, and atherosclerosis. The molecular mechanisms underlying ferroptosis include the iron-dependent accumulation of lipid peroxidation products, glutathione depletion, and dysregulation of lipid metabolism, among others. This review aims to summarize the current knowledge of the molecular mechanisms of ferroptosis in cardiovascular disease and discuss the potential therapeutic strategies targeting ferroptosis as a treatment for cardiovascular disease.

摘要

铁死亡是一种新发现的细胞程序性死亡方式,其特征是细胞内铁和脂质过氧化物的积累。研究表明,铁死亡在多种疾病的发病机制中发挥着重要作用,包括心血管疾病。在心血管疾病中,铁死亡与缺血再灌注损伤、心肌梗死、心力衰竭和动脉粥样硬化有关。铁死亡的分子机制包括铁依赖性脂质过氧化产物的积累、谷胱甘肽耗竭以及脂质代谢失调等。本综述旨在总结铁死亡在心血管疾病中的分子机制的最新知识,并讨论针对铁死亡的潜在治疗策略作为心血管疾病的治疗方法。

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