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阿尔茨海默病中的突触逆行发生与β-淀粉样蛋白

Synaptic retrogenesis and amyloid-beta in Alzheimer's disease.

作者信息

Wasling Pontus, Daborg Jonny, Riebe Ilse, Andersson My, Portelius Erik, Blennow Kaj, Hanse Eric, Zetterberg Henrik

机构信息

Department of Physiology, the Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

出版信息

J Alzheimers Dis. 2009;16(1):1-14. doi: 10.3233/JAD-2009-0918.

Abstract

Pathological hallmarks of Alzheimer's disease (AD) include synaptic and neuronal degeneration and the presence of extracellular deposits of amyloid-beta (Abeta) in senile plaques in the cerebral cortex. Although these brain lesions may be seen also in aged non-demented individuals, the increase in brain Abeta is believed by many to represent the earliest event in the disease process. Accumulating evidence suggests that Abeta, which is highly conserved by evolution, may have an important physiological role in synapse elimination during brain development. An intriguing idea is that this putative function can become pathogenic if activated in the aging brain. Here, we review the literature on the possible physiological roles of Abeta and its precursor protein AbetaPP during development with special focus on electrophysiological findings.

摘要

阿尔茨海默病(AD)的病理特征包括突触和神经元变性,以及大脑皮层老年斑中细胞外β淀粉样蛋白(Aβ)沉积物的存在。尽管这些脑部病变在未患痴呆症的老年人中也可见,但许多人认为大脑中Aβ的增加代表了疾病进程中的最早事件。越来越多的证据表明,在进化过程中高度保守的Aβ可能在大脑发育过程中的突触消除中具有重要的生理作用。一个有趣的观点是,如果这种假定的功能在衰老的大脑中被激活,它可能会致病。在这里,我们回顾了关于Aβ及其前体蛋白AβPP在发育过程中可能的生理作用的文献,特别关注电生理研究结果。

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