DNM1L型
神经保护
线粒体分裂
缺血
缺氧(环境)
氧化应激
粒体自噬
神经科学
线粒体
程序性细胞死亡
脑缺氧
线粒体通透性转换孔
医学
生物
药理学
细胞生物学
自噬
细胞凋亡
化学
内科学
生物化学
氧气
有机化学
作者
Huan Yu,Guangzhi Hao,Zuolin Shi,Yong Liang,Yushu Dong,Huilin Quan
标识
DOI:10.1016/j.biopha.2023.115247
摘要
Mitochondrial dysfunction, especially in terms of mitochondrial dynamics, has been reported to be closely associated with neuronal outcomes and neurological impairment in cerebral ischemia/hypoxia injury. Dynamin-related protein 1 (Drp1) is a cytoplasmic GTPase that mediates mitochondrial fission and participates in neuronal cell death, calcium signaling, and oxidative stress. The neuroprotective role of Drp1 inhibition has been confirmed in several central nervous system disease models, demonstrating that targeting Drp1 may shed light on novel approaches for the treatment of cerebral ischemia/hypoxia injury. In this review, we aimed to highlight the roles of Drp1 in programmed cell death, oxidative stress, mitophagy, and mitochondrial function to provide a better understanding of mitochondrial disturbances in cerebral ischemia/hypoxia injury, and we also summarize the advances in novel chemical compounds targeting Drp1 to provide new insights into potential therapies for cerebral ischemia/hypoxia injury.
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