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一种源自乙酰胆碱酯酶的肽是神经退行性变中的关键信号分子。

A peptide derived from acetylcholinesterase is a pivotal signalling molecule in neurodegeneration.

作者信息

Greenfield Susan

机构信息

University Department of Pharmacology, Mansfield Rd., Oxford OX1 3QT, UK.

出版信息

Chem Biol Interact. 2005 Dec 15;157-158:211-8. doi: 10.1016/j.cbi.2005.10.032. Epub 2005 Nov 17.

DOI:10.1016/j.cbi.2005.10.032
PMID:16297900
Abstract

It is now widely accepted that acetylcholinesterase (AChE) also displays non-cholinergic functions, completely independent of cholinergic transmission. Indeed, AChE has been implicated in a variety of trophic and toxic actions in a range of different systems. However, it is still uncertain what part of the AChE molecule may be responsible for these actions, and indeed via what receptor. Recent work has identified a peptide towards the C-terminus of the AChE molecule that appears to have very similar effects to non-cholinergic AChE itself. This action is to enhance calcium entry, in acute and chronic preparations across a trophic-toxic spectrum, depending on concentration applied and/or duration of exposure.

摘要

现在人们普遍认为,乙酰胆碱酯酶(AChE)也具有非胆碱能功能,这与胆碱能传递完全无关。事实上,AChE已被证明在一系列不同系统中具有多种营养和毒性作用。然而,仍不确定AChE分子的哪一部分可能负责这些作用,以及实际上是通过何种受体起作用。最近的研究发现,在AChE分子的C末端有一个肽,其作用似乎与非胆碱能AChE本身非常相似。这种作用是增强钙内流,在急性和慢性制剂中,跨越从营养到毒性的范围,这取决于所施加的浓度和/或暴露持续时间。

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