国际麻醉学与复苏杂志   2013, Issue (11): 1-1
    
突触功能障碍在阿尔茨海默病发病机制中的研究进展
蔡雨汐, 万燕杰, 徐静1()
1.徐州医学院江苏省麻醉学重点实验室
Recent advances of the roles of synaptic dysfunction in Alzheimer’s Disease
 全文:
摘要:

背景:神经突触具有高度可塑性,突触的形成和重塑是神经元活动依赖性的,是学习记忆、认知功能的基础。越来越多的证据表明阿尔茨海默病(Alzheimer’s disease,AD)早期出现的轻度认知功能下降与突触功能障碍相关。目的:对突触功能障碍在AD发病机制中的作用作一系统阐述。内容:近年来研究发现,AD患者脑内发生着明显的突触丢失的神经组织学改变,并多发生在认知缺失开始的早期;同时发现,突触的丢失程度与痴呆的严重程度密切相关,成为与认知缺失相关的一个重要的病理学特征。趋势:对突触功能障碍机制的深入研究可能为AD的早期干预和治疗开拓新的思路与方向。

关键词: 阿尔茨海默病;β-淀粉样蛋白;ADDLs;突触;树突棘;认知功能;Drebrin
Abstract:

Background Synapses are highly motile and can undergo remodeling even in the adult nervous system.Synapse remodeling and the formation of new synapses are activity-dependent processes that provide a basis for memory formation.There is growing evidence that mild cognitive impairment in early AD (Alzheimer’s disease) may be due to synaptic dysfunction.Objective To review the roles of synaptic dysfunction in Alzheimer’s Disease. Content Recent work suggests that loss of synapses is a evident histoneurological change in the early stages of cognitive deficiency in AD. The extent of snaptic loss has been found to be an excellent correlate of the degree of dementia, so it has been shown to be the best pathologic correlate of cognitive decline.Trend Further research into this area may provide useful insights and directions into the early intervention and treatment of Alzheimer’s disease.

Key words: Alzheimer’s disease;Aβ;ADDLs;Synapse;Dendritic spine;Cognitive function;Drebrin