发病机制
自噬
GPX4
氧化应激
程序性细胞死亡
疾病
医学
过氧化脂质
脂质过氧化
心肌病
细胞凋亡
心力衰竭
生物信息学
生物
免疫学
病理
内科学
超氧化物歧化酶
谷胱甘肽过氧化物酶
生物化学
作者
Sijie Jin,He Wang,Xiaohao Zhang,Mengyang Song,Bin Liu,Wei Sun
标识
DOI:10.1016/j.biopha.2024.116457
摘要
Ferroptosis, distinct from apoptosis, necrosis, autophagy, and other types of cell death, is a novel iron-dependent regulated cell death characterized by the accumulation of lipid peroxides and redox imbalance with distinct morphological, biochemical, and genetic features. Dysregulation of iron homeostasis, the disruption of antioxidative stress pathways and lipid peroxidation are crucial in ferroptosis. Ferroptosis is involved in the pathogenesis of several cardiovascular diseases, including atherosclerosis, cardiomyopathy, myocardial infarction, ischemia-reperfusion injury, abdominal aortic aneurysm, aortic dissection, and heart failure. Therefore, a comprehensive understanding of the mechanisms that regulate ferroptosis in cardiovascular diseases will enhance the prevention and treatment of these diseases. This review discusses the latest findings on the molecular mechanisms of ferroptosis and its regulation in cardiovascular diseases, the application of ferroptosis modulators in cardiovascular diseases, and the role of traditional Chinese medicines in ferroptosis regulation to provide a comprehensive understanding of the pathogenesis of cardiovascular diseases and identify new prevention and treatment options.
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