HIF-1α in myocardial ischemia-reperfusion injury

被引:115
作者
Zheng, Jie [1 ]
Chen, Peier [1 ]
Zhong, Jianfeng [2 ]
Cheng, Yu [1 ]
Chen, Hao [1 ]
He, Yuan [1 ]
Chen, Can [3 ]
机构
[1] Guangdong Med Univ, Lab Cardiovasc Dis, 57 Renmin Southern Rd, Zhanjiang 524000, Guangdong, Peoples R China
[2] Guangdong Med Univ, Guangdong Key Lab Age Related Cardiac & Cerebral, Affiliated Hosp, Zhanjiang 524001, Guangdong, Peoples R China
[3] Guangdong Med Univ, Dept Cardiol, Affiliated Hosp 2, 12 Minyou Rd, Zhanjiang 524003, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
hypoxia-inducible factor-1α ischemic heart disease; myocardial ischemia-reperfusion injury; mitochondrial function;
D O I
10.3892/mmr.2021.11991
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myocardial ischemia-reperfusion injury (MIRI) is a severe injury to the ischemic myocardium following the recovery of blood flow. Currently, there is no effective treatment for MIRI in clinical practice. Over the past two decades, biological studies of hypoxia and hypoxia-inducible factor-1 alpha (HIF-1 alpha) have notably improved understanding of oxygen homeostasis. HIF-1 alpha is an oxygen-sensitive transcription factor that mediates adaptive metabolic responses to hypoxia and serves a pivotal role in MIRI. In particular, previous studies have demonstrated that HIF-1 alpha improves mitochondrial function, decreases cellular oxidative stress, activates cardioprotective signaling pathways and downstream protective genes and interacts with non-coding RNAs. The present review summarizes the roles and associated mechanisms of action of HIF-1 alpha in MIRI. In addition, HIF-1 alpha-associated MIRI intervention, including natural compounds, exosomes, ischemic preconditioning and ischemic post-processing are presented. The present review provides evidence for the roles of HIF-1 alpha activation in MIRI and supports its use as a therapeutic target.
引用
收藏
页数:9
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