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脑缺血再灌注后神经可塑性的研究进展 被引量:9

Advances of Research on Neuronal Plasticity after Cerebral Ischemia-Reperfusion
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摘要 大脑对缺血再灌注损伤有一定代偿修复能力,可通过多种机制发生可塑性变化。脑内与缺血再灌注有关的可塑性物质主要有突触素(synaptophysin,Syn)、生长相关蛋白-43(growth-associatedprotein-43,GAP-43)及微管相关蛋白-2(microtubule-associated protein-2,MAP-2)等物质,它们通过各自途径影响脑缺血再灌注后脑的可塑性变化,而可塑性变化又受到生存环境、康复训练、药物治疗等因素的影响。 The brain has a capacity of repairing ischemia reperfusion injury. Through various mechanisms, the brain develops a plastically change. The plastically substances of the internal brain which is related to ischemia reperfusion injury are mainly the followings: synaptophysin(Syn), growth-associated protein-43(GAP-43) and microtubule-associated protein-2(MAP-2), etc. By kinds of means, they infect the plastically change of ischemia reperfusion injury respectively. But the change is also influenced by factors such as the living surroundings, rehabilitation training and pharmacotherapy, etc.
出处 《中国卒中杂志》 2012年第11期902-906,共5页 Chinese Journal of Stroke
基金 国家重点基础研究发展计划(973计划)项目(2009CB522900) 国家自然科学基金项目(81001547)
关键词 缺血再灌注 可塑性 Ischemia-reperfusion Plasticity
作者简介 通信作者 徐鸣曙 mingshuxu@yahoo.com.cn
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