4.7 Review

Mechanisms of neuronal cell death in ischemic stroke and their therapeutic implications

Journal

MEDICINAL RESEARCH REVIEWS
Volume 42, Issue 1, Pages 259-305

Publisher

WILEY
DOI: 10.1002/med.21817

Keywords

apoptosis; ferroptosis; ischemic stroke; neuronal death; neuroprotection

Funding

  1. Ministry of Science and Technology of the People's Republic of China [2018YFC1312300]
  2. China Postdoctoral Science Foundation [2017M623041, 2019T120848]
  3. National Natural Science Foundation of China [81722016, 81801182, 82071191]
  4. Post Doctor Research Program of West China Hospital, Sichuan University [2018HXBH044]
  5. National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University [Z2018B03]

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Ischemic stroke caused by arterial occlusion is a common type of stroke that involves multiple cell death pathways such as apoptosis, necroptosis, and autophagy. Understanding these pathways may reveal new neuroprotective interventions for ischemic stroke.
Ischemic stroke caused by arterial occlusion is the most common type of stroke, which is among the most frequent causes of disability and death worldwide. Current treatment approaches involve achieving rapid reperfusion either pharmacologically or surgically, both of which are time-sensitive; moreover, blood flow recanalization often causes ischemia/reperfusion injury. However, even though neuroprotective intervention is urgently needed in the event of stroke, the exact mechanisms of neuronal death during ischemic stroke are still unclear, and consequently, the capacity for drug development has remained limited. Multiple cell death pathways are implicated in the pathogenesis of ischemic stroke. Here, we have reviewed these potential neuronal death pathways, including intrinsic and extrinsic apoptosis, necroptosis, autophagy, ferroptosis, parthanatos, phagoptosis, and pyroptosis. We have also reviewed the latest results of pharmacological studies on ischemic stroke and summarized emerging drug targets with a focus on clinical trials. These observations may help to further understand the pathological events in ischemic stroke and bridge the gap between basic and translational research to reveal novel neuroprotective interventions.

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