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尼古丁通过激活α7-烟碱型乙酰胆碱受体防止淀粉样β寡聚体诱导的突触损伤。

Nicotine prevents synaptic impairment induced by amyloid-β oligomers through α7-nicotinic acetylcholine receptor activation.

机构信息

Centro de Envejecimiento y Regeneración (CARE), Pontificia Universidad Católica de Chile, PO Box 114-D, Santiago, Chile.

出版信息

Neuromolecular Med. 2013 Sep;15(3):549-69. doi: 10.1007/s12017-013-8242-1. Epub 2013 Jul 11.

Abstract

An emerging view on Alzheimer disease's (AD) pathogenesis considers amyloid-β (Aβ) oligomers as a key factor in synaptic impairment and rodent spatial memory decline. Alterations in the α7-nicotinic acetylcholine receptor (α7-nAChR) have been implicated in AD pathology. Herein, we report that nicotine, an unselective α7-nAChR agonist, protects from morphological and synaptic impairments induced by Aβ oligomers. Interestingly, nicotine prevents both early postsynaptic impairment and late presynaptic damage induced by Aβ oligomers through the α7-nAChR/phosphatidylinositol-3-kinase (PI3K) signaling pathway. On the other hand, a cross-talk between α7-nAChR and the Wnt/β-catenin signaling pathway was revealed by the following facts: (1) nicotine stabilizes β-catenin, in a concentration-dependent manner; (2) nicotine prevents Aβ-induced loss of β-catenin through the α7-nAChR; and (3) activation of canonical Wnt/β-catenin signaling induces α7-nAChR expression. Analysis of the α7-nAChR promoter indicates that this receptor is a new Wnt target gene. Taken together, these results demonstrate that nicotine prevents memory deficits and synaptic impairment induced by Aβ oligomers. In addition, nicotine improves memory in young APP/PS1 transgenic mice before extensive amyloid deposition and senile plaque development, and also in old mice where senile plaques have already formed. Activation of the α7-nAChR/PI3K signaling pathway and its cross-talk with the Wnt signaling pathway might well be therapeutic targets for potential AD treatments.

摘要

阿尔茨海默病(AD)发病机制的一个新观点认为,淀粉样β(Aβ)寡聚体是突触损伤和啮齿动物空间记忆下降的关键因素。α7-烟碱型乙酰胆碱受体(α7-nAChR)的改变与 AD 病理有关。本文报道,非选择性α7-nAChR 激动剂尼古丁可防止 Aβ寡聚体引起的形态和突触损伤。有趣的是,尼古丁通过α7-nAChR/磷酸肌醇-3-激酶(PI3K)信号通路防止 Aβ寡聚体引起的早期突触后损伤和晚期突触前损伤。另一方面,α7-nAChR 与 Wnt/β-连环蛋白信号通路之间的串扰由以下事实揭示:(1)尼古丁以浓度依赖的方式稳定β-连环蛋白;(2)尼古丁通过α7-nAChR 防止 Aβ 诱导的β-连环蛋白丢失;(3)激活经典 Wnt/β-连环蛋白信号诱导α7-nAChR 表达。α7-nAChR 启动子分析表明,该受体是 Wnt 的新靶基因。总之,这些结果表明,尼古丁可防止 Aβ 寡聚体引起的记忆缺陷和突触损伤。此外,尼古丁可改善年轻 APP/PS1 转基因小鼠在大量淀粉样蛋白沉积和老年斑形成之前以及在已经形成老年斑的老年小鼠中的记忆。激活α7-nAChR/PI3K 信号通路及其与 Wnt 信号通路的串扰可能是 AD 潜在治疗的治疗靶点。

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