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凋亡途径在阿尔茨海默病神经退行性变和细胞死亡中的作用。

The role of apoptotic pathways in Alzheimer's disease neurodegeneration and cell death.

作者信息

LeBlanc Andrea C

机构信息

Department of Neurology and Neurosurgery, McGill University, 3775 University St., Montreal, Quebec Canada H3A 2B4.

出版信息

Curr Alzheimer Res. 2005 Oct;2(4):389-402. doi: 10.2174/156720505774330573.

Abstract

Neuronal loss is associated with Alzheimer's disease (AD). However, it not clear what type of mechanisms underlie this neuronal loss and if neuronal loss is directly responsible for the progressive dementia of AD. This review summarizes the recent evidence for neuronal loss in AD relative to the level of cognitive impairment. It further describes the current evidence for an apoptotic mechanism in AD. Lastly, a summary of the evidence for synaptic loss being responsible for dementia rather than neuronal loss is presented. A novel hypothesis emerges from this data to explain all aspects of AD pathophysiology. This all inclusive hypothesis called the attrition hypothesis states that activation of the effector caspase-6 in AD due to one or a variety of insults is responsible for the breakdown of the cytoskeletal structure of neurites and damages proper trafficking of proteins and organelles thus resulting in the observed clinical and pathological features of AD.

摘要

神经元丢失与阿尔茨海默病(AD)相关。然而,尚不清楚这种神经元丢失背后的机制类型,以及神经元丢失是否直接导致AD的进行性痴呆。本综述总结了近期关于AD中神经元丢失与认知障碍水平相关的证据。它进一步描述了AD中凋亡机制的当前证据。最后,总结了支持突触丢失而非神经元丢失导致痴呆的证据。基于这些数据出现了一个新的假说来解释AD病理生理学的各个方面。这个涵盖所有方面的假说称为磨损假说,即由于一种或多种损伤导致AD中效应半胱天冬酶-6的激活,负责神经突细胞骨架结构的破坏,并损害蛋白质和细胞器的正常运输,从而导致观察到的AD临床和病理特征。

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