Targeting Ferroptosis as a Promising Therapeutic Strategy for Ischemia-Reperfusion Injury

被引:79
作者
Pan, Yihang [1 ]
Wang, Xueke [1 ]
Liu, Xiwang [2 ]
Shen, Lihua [1 ]
Chen, Qixing [1 ,3 ]
Shu, Qiang [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Natl Clin Res Ctr Child Hlth, Sch Med, Dept Clin Res Ctr,Childrens Hosp, Hangzhou 310052, Peoples R China
[2] Zhejiang Univ, Childrens Hosp, Sch Med, Dept Thorac & Cardiovasc Surg, Hangzhou 310003, Peoples R China
[3] Key Lab Diag & Treatment Neonatal Dis Zhejiang Pr, Hangzhou 310052, Peoples R China
基金
中国国家自然科学基金;
关键词
ischemia-reperfusion injury; ferroptosis; iron; antioxidant; therapeutic strategies; CEREBRAL-ARTERY OCCLUSION; CELL-DEATH; PROMOTES FERROPTOSIS; LIPID-PEROXIDATION; RAT MODEL; IN-VIVO; IRON; ACTIVATION; KIDNEY; DAMAGE;
D O I
10.3390/antiox11112196
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ischemia-reperfusion (I/R) injury is a major challenge in perioperative medicine that contributes to pathological damage in various conditions, including ischemic stroke, myocardial infarction, acute lung injury, liver transplantation, acute kidney injury and hemorrhagic shock. I/R damage is often irreversible, and current treatments for I/R injury are limited. Ferroptosis, a type of regulated cell death characterized by the iron-dependent accumulation of lipid hydroperoxides, has been implicated in multiple diseases, including I/R injury. Emerging evidence suggests that ferroptosis can serve as a therapeutic target to alleviate I/R injury, and pharmacological strategies targeting ferroptosis have been developed in I/R models. Here, we systematically summarize recent advances in research on ferroptosis in I/R injury and provide a comprehensive analysis of ferroptosis-regulated genes investigated in the context of I/R, as well as the therapeutic applications of ferroptosis regulators, to provide insights into developing therapeutic strategies for this devastating disease.
引用
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页数:25
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