Crosstalk between the M1 muscarinic acetylcholine receptor and the endocannabinoid system: A relevance for Alzheimer's disease?

被引:20
|
作者
Thompson, Karen J. [1 ]
Tobin, Andrew B. [1 ]
机构
[1] Univ Glasgow, Ctr Translat Pharmacol, Inst Mol Cell & Syst Biol, Davidson Bldg, Glasgow G12 8QQ, Lanark, Scotland
基金
英国惠康基金;
关键词
Alzheimer; Acetylcholine; Cannabinoid; Crosstalk; Cholinergic; Endocannabinoid; ALPHA-7 NICOTINIC ACETYLCHOLINE; CB1 CANNABINOID RECEPTORS; INCREASES INTRACELLULAR CALCIUM; CELL-CULTURE MODEL; CHOLINERGIC HYPOTHESIS; MONOACYLGLYCEROL LIPASE; CONCURRENT STIMULATION; ALLOSTERIC MODULATOR; SYNAPTIC PLASTICITY; INTERNATIONAL UNION;
D O I
10.1016/j.cellsig.2020.109545
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder which accounts for 60-70% of the 50 million world-wide cases of dementia and is characterised by cognitive impairments, many of which have long been associated with dysfunction of the cholinergic system. Although the M-1 muscarinic acetylcholine receptor (mAChR) is considered a promising drug target for AD, ligands targeting this receptor have so far been unsuccessful in clinical trials. As modulatory receptors to cholinergic transmission, the endocannabinoid system may be a promising drug target to allow fine tuning of the cholinergic system. Furthermore, disease-related changes have been found in the endocannabinoid system during AD progression and indeed targeting the endocannabinoid system at specific disease stages alleviates cognitive symptoms in numerous mouse models of AD. Here we review the role of the endocannabinoid system in AD, and its crosstalk with mAChRs as a potential drug target for cholinergic dysfunction.
引用
收藏
页数:11
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