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本文引用的文献

1
Scopolamine disrupts place navigation in rats and humans: a translational validation of the Hidden Goal Task in the Morris water maze and a real maze for humans.东莨菪碱会干扰大鼠和人类的空间导航:对莫里斯水迷宫中隐藏目标任务以及人类真实迷宫任务的转化验证。
Psychopharmacology (Berl). 2017 Feb;234(4):535-547. doi: 10.1007/s00213-016-4488-2. Epub 2016 Nov 24.
2
Distribution of muscarinic acetylcholine receptor subtypes in the murine small intestine.毒蕈碱型乙酰胆碱受体亚型在小鼠小肠中的分布。
Life Sci. 2017 Jan 15;169:6-10. doi: 10.1016/j.lfs.2016.10.030. Epub 2016 Nov 17.
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Multi-target-directed therapeutic potential of 7-methoxytacrine-adamantylamine heterodimers in the Alzheimer's disease treatment.7-甲氧基他克林-金刚烷胺杂二聚体在阿尔茨海默病治疗中的多靶点治疗潜力。
Biochim Biophys Acta Mol Basis Dis. 2017 Feb;1863(2):607-619. doi: 10.1016/j.bbadis.2016.11.020. Epub 2016 Nov 16.
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Network mechanisms of hippocampal laterality, place coding, and goal-directed navigation.海马体偏侧化、位置编码和目标导向导航的网络机制。
J Physiol Sci. 2017 Mar;67(2):247-258. doi: 10.1007/s12576-016-0502-z. Epub 2016 Nov 18.
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Nicotinic regulation of experience-dependent plasticity in visual cortex.视觉皮层中烟碱对经验依赖性可塑性的调节作用
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3-iodothyronamine (T1AM), a novel antagonist of muscarinic receptors.3-碘甲腺原氨酸(T1AM),一种新型毒蕈碱受体拮抗剂。
Eur J Pharmacol. 2016 Dec 15;793:35-42. doi: 10.1016/j.ejphar.2016.10.027. Epub 2016 Nov 2.
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Neuronal Nicotinic Receptors Are Crucial for Tuning of E/I Balance in Prelimbic Cortex and for Decision-Making Processes.神经元烟碱受体对于前边缘皮层中兴奋/抑制平衡的调节以及决策过程至关重要。
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8
The challenges of modulating the 'rest and digest' system: acetylcholine receptors as drug targets.调节“休息与消化”系统的挑战:乙酰胆碱受体作为药物靶点
Drug Discov Today. 2017 Jan;22(1):97-104. doi: 10.1016/j.drudis.2016.09.011. Epub 2016 Sep 22.
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Cholinergic circuits in cognitive flexibility.认知灵活性中的胆碱能回路。
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Locating and navigation mechanism based on place-cell and grid-cell models.基于位置细胞和网格细胞模型的定位与导航机制。
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干扰毒蕈碱型乙酰胆碱受体的药物及其对空间导航的影响。

Drugs Interfering with Muscarinic Acetylcholine Receptors and Their Effects on Place Navigation.

作者信息

Svoboda Jan, Popelikova Anna, Stuchlik Ales

机构信息

Institute of Physiology of the Czech Academy of Sciences, Prague, Czechia.

出版信息

Front Psychiatry. 2017 Nov 9;8:215. doi: 10.3389/fpsyt.2017.00215. eCollection 2017.

DOI:10.3389/fpsyt.2017.00215
PMID:29170645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5684124/
Abstract

Muscarinic acetylcholine receptors (mAChRs) have been found to regulate many diverse functions, ranging from motivation and feeding to spatial navigation, an important and widely studied type of cognitive behavior. Systemic administration of non-selective antagonists of mAChRs, such as scopolamine or atropine, have been found to have adverse effects on a vast majority of place navigation tasks. However, many of these results may be potentially confounded by disruptions of functions other than spatial learning and memory. Although studies with selective antimuscarinics point to mutually opposite effects of M1 and M2 receptors, their particular contribution to spatial cognition is still poorly understood, partly due to a lack of truly selective agents. Furthermore, constitutive knock-outs do not always support results from selective antagonists. For modeling impaired spatial cognition, the scopolamine-induced amnesia model still maintains some limited validity, but there is an apparent need for more targeted approaches such as local intracerebral administration of antagonists, as well as novel techniques such as optogenetics focused on cholinergic neurons and chemogenetics aimed at cells expressing metabotropic mAChRs.

摘要

已发现毒蕈碱型乙酰胆碱受体(mAChRs)可调节多种不同功能,从动机和摄食到空间导航,空间导航是一种重要且被广泛研究的认知行为类型。已发现全身给予mAChRs的非选择性拮抗剂,如东莨菪碱或阿托品,会对绝大多数位置导航任务产生不利影响。然而,许多这些结果可能会因空间学习和记忆以外的功能破坏而受到潜在混淆。尽管使用选择性抗毒蕈碱药物的研究表明M1和M2受体具有相互相反的作用,但它们对空间认知的具体贡献仍知之甚少,部分原因是缺乏真正的选择性药物。此外,组成型基因敲除并不总是支持选择性拮抗剂的结果。对于模拟受损的空间认知,东莨菪碱诱导的失忆模型仍具有一定的有限有效性,但显然需要更具针对性的方法,如局部脑内给予拮抗剂,以及诸如针对胆碱能神经元的光遗传学和针对表达代谢型mAChRs的细胞的化学遗传学等新技术。