缺氧(环境)
神经炎症
调节器
小胶质细胞
缺血
冲程(发动机)
医学
血管生成
神经科学
溶栓
脑缺血
缺血性中风
神经保护
缺氧诱导因子
药理学
血脑屏障
生物信息学
中枢神经系统
免疫学
内科学
生物
炎症
化学
心肌梗塞
机械工程
生物化学
有机化学
氧气
工程类
基因
作者
Sneha Vatte,Rajesh R. Ugale
标识
DOI:10.1016/j.neuint.2023.105605
摘要
Ischemic stroke is a leading cause of disability and mortality worldwide due to the narrow therapeutic window of the only approved therapies like intravenous thrombolysis and thrombectomy. Hypoxia inducible factor-1α (HIF-1α) is a sensitive regulator of oxygen homeostasis, and its expression is rapidly induced after hypoxia/ischemia. It plays an extensive role in the pathophysiology of stroke by regulating multiple pathways including glucose metabolism, angiogenesis, neuronal survival, neuroinflammation and blood brain barrier regulation. Here, we give a brief overview of the HIF-1α-targeting strategies currently under investigation and summarise recent research on how HIF-1α is regulated in various brain cells, including neurons and microglia, at various stages in ischemic stroke. The roles of HIF-1 in stroke varies with ischemic time and degree of ischemia, are still up for debate. More focus has been placed on prospective HIF-1α targeting drugs, such as HIF-1α activator, HIF-1α stabilizers, and natural compounds. In this review, we have highlighted the regulation of HIF-1α in the novel therapeutic approaches for treatment of stroke.
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