神经保护
程序性细胞死亡
上睑下垂
医学
自噬
兴奋毒性
冲程(发动机)
缺血
神经科学
半影
炎症
细胞凋亡
坏死性下垂
生物信息学
药理学
免疫学
生物
炎症体
内科学
机械工程
工程类
生物化学
作者
Emine Şekerdağ,İhsan Solaroğlu,Yasemin Özdemir
出处
期刊:Current Neuropharmacology
[Bentham Science]
日期:2018-03-07
卷期号:16 (9): 1396-1415
被引量:281
标识
DOI:10.2174/1570159x16666180302115544
摘要
As a result of ischemia or hemorrhage, blood supply to neurons is disrupted which subsequently promotes a cascade of pathophysiological responses resulting in cell loss. Many mechanisms are involved solely or in combination in this disorder including excitotoxicity, mitochondrial death pathways, and the release of free radicals, protein misfolding, apoptosis, necrosis, autophagy and inflammation. Besides neuronal cell loss, damage to and loss of astrocytes as well as injury to white matter contributes also to cerebral injury. The core problem in stroke is the loss of neuronal cells which makes recovery difficult or even not possible in the late states. Acute treatment options that can be applied for stroke are mainly targeting re-establishment of blood flow and hence, their use is limited due to the effective time window of thrombolytic agents. However, if the acute time window is exceeded, neuronal loss starts due to the activation of cell death pathways. This review will explore the most updated cellular death mechanisms leading to neuronal loss in stroke. Ischemic and hemorrhagic stroke as well as subarachnoid hemorrhage will be debated in the light of cell death mechanisms and possible novel molecular and cellular treatment options will be discussed.
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