Targeting the M1 muscarinic acetylcholine receptor in Alzheimer's disease.

Q4 Neuroscience Neuronal signaling Pub Date : 2022-04-21 eCollection Date: 2022-04-01 DOI:10.1042/NS20210004
Louis Dwomoh, Gonzalo S Tejeda, Andrew B Tobin
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Abstract

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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靶向M1毒蕈碱乙酰胆碱受体治疗阿尔茨海默病
摘要阿尔茨海默病(AD)仍然是全球发病率和死亡率的主要原因,尽管进行了广泛的研究,但只有少数药物可用于治疗该疾病。一种策略是上调胆碱能神经传递以改善认知功能,但这种方法具有剂量限制的副作用。为了避免这些不良反应,需要靶向胆碱能系统特异性受体亚型的新药,而毒蕈碱乙酰胆碱受体的M1亚型(M1 mAChR)已被证明是这种方法的良好靶点。通过使用几种策略,M1 mAChR配体已在临床前动物模型和人体研究中得到开发和试验,并取得了不同程度的成功。本文综述了针对AD中M1 mAChR的不同方法,并讨论了这些策略的优势和局限性。还讨论了在AD中靶向M1 mAChR时需要考虑的因素。
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来源期刊
CiteScore
4.60
自引率
0.00%
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0
审稿时长
14 weeks
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