HIF-1是缺血性脑卒中潜在新治疗方法中的重要调节因子。

IF 4.4 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Neurochemistry international Pub Date : 2023-11-01 DOI:10.1016/j.neuint.2023.105605
Sneha Vatte, Rajesh Ugale
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引用次数: 0

摘要

缺血性中风是世界范围内致残和死亡的主要原因,因为只有静脉溶栓和血栓切除等获批疗法的治疗窗口很窄。缺氧诱导因子-1α(HIF-1α)是一种敏感的氧稳态调节因子,其表达在缺氧/缺血后迅速诱导。它通过调节多种途径,包括葡萄糖代谢、血管生成、神经元存活、神经炎症和血脑屏障调节,在中风的病理生理学中发挥着广泛的作用。在这里,我们简要概述了目前正在研究的HIF-1α靶向策略,并总结了最近关于HIF-1α在缺血性中风不同阶段如何在包括神经元和小胶质细胞在内的各种脑细胞中调节的研究。HIF-1在脑卒中中的作用随着缺血时间和缺血程度的不同而不同,仍有争议。人们越来越关注未来的HIF-1α靶向药物,如HIF-1α激活剂、HIF-1α稳定剂和天然化合物。在这篇综述中,我们强调了HIF-1α在中风治疗新方法中的调节作用。
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HIF-1, an important regulator in potential new therapeutic approaches to ischemic stroke

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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来源期刊
Neurochemistry international
Neurochemistry international 医学-神经科学
CiteScore
8.40
自引率
2.40%
发文量
128
审稿时长
37 days
期刊介绍: Neurochemistry International is devoted to the rapid publication of outstanding original articles and timely reviews in neurochemistry. Manuscripts on a broad range of topics will be considered, including molecular and cellular neurochemistry, neuropharmacology and genetic aspects of CNS function, neuroimmunology, metabolism as well as the neurochemistry of neurological and psychiatric disorders of the CNS.
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