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Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease

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 d...

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Detalles Bibliográficos
Autores principales: Dwomoh, Louis, Tejeda, Gonzalo S., Tobin, Andrew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069568/
https://www.ncbi.nlm.nih.gov/pubmed/35571495
http://dx.doi.org/10.1042/NS20210004
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author Dwomoh, Louis
Tejeda, Gonzalo S.
Tobin, Andrew B.
author_facet Dwomoh, Louis
Tejeda, Gonzalo S.
Tobin, Andrew B.
author_sort Dwomoh, Louis
collection PubMed
description 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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spelling pubmed-90695682022-05-12 Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease Dwomoh, Louis Tejeda, Gonzalo S. Tobin, Andrew B. Neuronal Signal Neuroscience 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. Portland Press Ltd. 2022-04-21 /pmc/articles/PMC9069568/ /pubmed/35571495 http://dx.doi.org/10.1042/NS20210004 Text en © 2022 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Neuroscience
Dwomoh, Louis
Tejeda, Gonzalo S.
Tobin, Andrew B.
Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title_full Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title_fullStr Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title_full_unstemmed Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title_short Targeting the M1 muscarinic acetylcholine receptor in Alzheimer’s disease
title_sort targeting the m1 muscarinic acetylcholine receptor in alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069568/
https://www.ncbi.nlm.nih.gov/pubmed/35571495
http://dx.doi.org/10.1042/NS20210004
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