Myocardial Ischemia/Reperfusion Injury: Mechanism and Targeted Treatment for Ferroptosis

被引:1
|
作者
Deng, Yun [1 ]
Chen, Qiaoling [1 ]
Wang, Tianyu [2 ]
Wang, Shuangcui [1 ]
Li, Ruoyun [3 ]
Wang, Yuli [1 ]
Zhang, Jiaqi [1 ]
Gan, Jiali [1 ]
Guo, Maojuan [1 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Sch Integrat Med, Tianjin, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Sch Med Technol, Tianjin, Peoples R China
[3] Tianjin Univ Tradit Chinese Med, Sch Tradit Chinese Med, Tianjin, Peoples R China
来源
ANATOLIAN JOURNAL OF CARDIOLOGY | 2024年 / 28卷 / 03期
基金
中国国家自然科学基金;
关键词
Myocardial ischemia/reperfusion injury; ferroptosis; pathological mechanism; targeted therapy; CELL-DEATH; REPERFUSION INJURY;
D O I
10.14744/AnatolJCardiol.2023.3606
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myocardial ischemia/reperfusion injury (MIRI) is a pathophysiological process connected to the onset of numerous heart disorders. The pathogenesis of MIRI is complex, and it mainly involves calcium overload, classic oxidative stress, mitochondrial disorder, inflammation, microvascular disorder, and cell death. The clinical treatment options for MIRI are presently constrained, making it imperative to develop new treatment modalities. Recent studies have demonstrated that ferroptosis is the main cause of MIRI. Ferroptosis is a new type of regulated iron-dependent cell death whose mechanism and targeted therapy are anticipated to be novel therapeutic techniques for MIRI. Herein, the primary mechanism underlying ferroptosis (the 3 major metabolic routes involving iron, amino acids, and lipids, and in MIRI, the specific mechanism and therapeutic target of ferroptosis) are discussed to determine the potential therapeutic approach for MIRI.
引用
收藏
页码:133 / 141
页数:9
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