靶向M1毒蕈碱乙酰胆碱受体治疗阿尔茨海默病

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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引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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 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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来源期刊
CiteScore
4.60
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