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受烟碱型乙酰胆碱受体调控的神经网络系统:新假说。

Neural systems governed by nicotinic acetylcholine receptors: emerging hypotheses.

机构信息

Division of Biology, California Institute of Technology, 1200 E. California Boulevard, Pasadena, CA 91125, USA.

出版信息

Neuron. 2011 Apr 14;70(1):20-33. doi: 10.1016/j.neuron.2011.03.014.

DOI:10.1016/j.neuron.2011.03.014
PMID:21482353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4418790/
Abstract

Cholinergic neurons and nicotinic acetylcholine receptors (nAChRs) in the brain participate in diverse functions: reward, learning and memory, mood, sensory processing, pain, and neuroprotection. Nicotinic systems also have well-known roles in drug abuse. Here, we review recent insights into nicotinic function, linking exogenous and endogenous manipulations of nAChRs to alterations in synapses, circuits, and behavior. We also discuss how these contemporary advances can motivate attempts to exploit nicotinic systems therapeutically in Parkinson's disease, cognitive decline, epilepsy, and schizophrenia.

摘要

大脑中的胆碱能神经元和烟碱型乙酰胆碱受体 (nAChRs) 参与多种功能:奖励、学习和记忆、情绪、感觉处理、疼痛和神经保护。尼古丁系统在药物滥用中也有众所周知的作用。在这里,我们回顾了尼古丁功能的最新见解,将 nAChR 的外源性和内源性操作与突触、回路和行为的改变联系起来。我们还讨论了这些当代进展如何激发人们尝试在帕金森病、认知能力下降、癫痫和精神分裂症中利用尼古丁系统进行治疗。

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本文引用的文献

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Short- and long-lasting consequences of in vivo nicotine treatment on hippocampal excitability.体内给予尼古丁处理对海马兴奋性的短期和长期后果。
J Neurosci. 2011 Feb 16;31(7):2584-94. doi: 10.1523/JNEUROSCI.4362-10.2011.
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Habenula "cholinergic" neurons co-release glutamate and acetylcholine and activate postsynaptic neurons via distinct transmission modes.缰核“胆碱能”神经元共同释放谷氨酸和乙酰胆碱,并通过不同的传递模式激活突触后神经元。
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Habenular α5 nicotinic receptor subunit signalling controls nicotine intake.缰核 α5 型烟碱型乙酰胆碱受体亚基信号传导控制尼古丁摄入。
Nature. 2011 Mar 31;471(7340):597-601. doi: 10.1038/nature09797. Epub 2011 Jan 30.
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NMR structure and action on nicotinic acetylcholine receptors of water-soluble domain of human LYNX1.人 LYNX1 水溶性结构域的 NMR 结构与烟碱型乙酰胆碱受体作用
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Nicotine up-regulates alpha4beta2 nicotinic receptors and ER exit sites via stoichiometry-dependent chaperoning.尼古丁通过依赖于化学计量的伴侣蛋白介导而上调α4β2 型烟碱型乙酰胆碱受体和内质网出口部位。
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