Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
Author(s) -
Louis Dwomoh,
Gonzalo S. Tejeda,
Andrew Tobin
Publication year - 2022
Publication title -
neuronal signaling
Language(s) - English
Resource type - Journals
ISSN - 2059-6553
DOI - 10.1042/ns20210004
Subject(s) - muscarinic acetylcholine receptor , acetylcholine , cholinergic , disease , adverse effect , neuroscience , medicine , acetylcholine receptor , alzheimer's disease , limiting , receptor , bioinformatics , pharmacology , biology , mechanical engineering , engineering
Alzheimer’s disease (AD) remains a major cause of morbidity and mortality worldwide, and despite extensive research, only a few drugs are available for management of the disease. One strategy has been to up-regulate cholinergic neurotransmission to improve cognitive function, but this approach has dose-limiting adverse effects. To avoid these adverse effects, new drugs that target specific receptor subtypes of the cholinergic system are needed, and the M1 subtype of muscarinic acetylcholine receptor (M1-mAChR) has been shown to be a good target for this approach. By using several strategies, M1-mAChR ligands have been developed and trialled in preclinical animal models and in human studies, with varying degrees of success. This article reviews the different approaches to targeting the M1-mAChR in AD and discusses the advantages and limitations of these strategies. The factors to consider in targeting the M1-mAChR in AD are also discussed.
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