少突胶质细胞
白质
神经科学
谷氨酸受体
髓鞘
缺血
多发性硬化
医学
缺氧(环境)
室周白质软化
冲程(发动机)
兴奋毒性
氧化应激
中枢神经系统
生物
受体
免疫学
内科学
磁共振成像
化学
氧气
有机化学
胎龄
怀孕
工程类
放射科
机械工程
遗传学
作者
Gabriella Mifsud,Christian Zammit,Richard Muscat,Giuseppe Di Giovanni,Mario Valentino
摘要
Summary Oligodendrocytes ( OL s), the myelin‐forming cells of the central nervous system, form a functional unit with axons and play a crucial role in axonal integrity. An episode of hypoxia–ischemia causes rapid and severe damage to these particularly vulnerable cells via multiple pathways such as overactivation of glutamate and ATP receptors, oxidative stress, and disruption of mitochondrial function. The cardinal effect of OL pathology is demyelination and dysmyelination, and this has profound effects on axonal function, transport, structure, metabolism, and survival. The OL is a primary target of ischemia in adult‐onset stroke and especially in periventricular leukomalacia and should be considered as a primary therapeutic target in these conditions. More emphasis is needed on therapeutic strategies that target OL s, myelin, and their receptors, as these have the potential to significantly attenuate white matter injury and to establish functional recovery of white matter after stroke. In this review, we will summarize recent progress on the role of OL s in white matter ischemic injury and the current and emerging principles that form the basis for protective strategies against OL death.
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