Neuronal Death Mechanisms and Therapeutic Strategy in Ischemic Stroke

被引:124
|
作者
Mao, Rui [1 ]
Zong, Ningning [1 ]
Hu, Yujie [1 ]
Chen, Ying [1 ]
Xu, Yun [1 ,2 ,3 ,4 ,5 ]
机构
[1] Nanjing Univ, Dept Neurol, Affiliated Drum Tower Hosp, Med Sch, Nanjing 210008, Peoples R China
[2] Nanjing Univ, Inst Brain Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210008, Peoples R China
[3] Nanjing Univ, Jiangsu Key Lab Mol Med, Med Sch, Nanjing 210008, Peoples R China
[4] Jiangsu Prov Stroke Ctr Diag & Therapy, Nanjing 210008, Peoples R China
[5] Nanjing Neurol Clin Med Ctr, Nanjing 210008, Peoples R China
基金
中国国家自然科学基金;
关键词
Ischemic stroke; Neuronal death; Mechanisms; Therapeutic strategy; D-ASPARTATE RECEPTORS; OXIDATIVE STRESS; CELL-DEATH; BRAIN-DAMAGE; MICROGLIAL PHAGOCYTOSIS; MOLECULAR-MECHANISMS; SIGNALING PATHWAY; NITRIC-OXIDE; DOUBLE-BLIND; T-CELLS;
D O I
10.1007/s12264-022-00859-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ischemic stroke caused by intracranial vascular occlusion has become increasingly prevalent with considerable mortality and disability, which gravely burdens the global economy. Current relatively effective clinical treatments are limited to intravenous alteplase and thrombectomy. Even so, patients still benefit little due to the short therapeutic window and the risk of ischemia/reperfusion injury. It is therefore urgent to figure out the neuronal death mechanisms following ischemic stroke in order to develop new neuroprotective strategies. Regarding the pathogenesis, multiple pathological events trigger the activation of cell death pathways. Particular attention should be devoted to excitotoxicity, oxidative stress, and inflammatory responses. Thus, in this article, we first review the principal mechanisms underlying neuronal death mediated by these significant events, such as intrinsic and extrinsic apoptosis, ferroptosis, parthanatos, pyroptosis, necroptosis, and autophagic cell death. Then, we further discuss the possibility of interventions targeting these pathological events and summarize the present pharmacological achievements.
引用
收藏
页码:1229 / 1247
页数:19
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