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重新构想胆碱能疗法治疗阿尔茨海默病。

Reimagining cholinergic therapy for Alzheimer's disease.

机构信息

Department of Internal Medicine, Readaptation and Geriatrics, Faculty of Medicine, University of Geneva Hospitals, University of Geneva, CH 1226 Geneva, Switzerland.

Department of Pharmacology, McGill University, H3G 1Y6 Montreal, Canada.

出版信息

Brain. 2022 Jul 29;145(7):2250-2275. doi: 10.1093/brain/awac096.

Abstract

Currently, enhancement of cholinergic neurotransmission via cholinesterase inhibitors represents the main available approach to treat cognitive and behavioural symptoms of the early as well as late stages of Alzheimer's disease. Restoring the cholinergic system has been a primary means of improving cognition in Alzheimer's disease, as four of the six approved therapies are acetylcholinesterase inhibitors. Memantine is an N-methyl-d-aspartate antagonist with a well-documented clinical effect on behavioural symptoms, which is often added to cholinesterase inhibitors to potentiate their effect and aducanumab, targeting the amyloid pathology, has recently been approved. The early, progressive and selective degeneration of the cholinergic system together and its close relation to cognitive deficits supports the use of cholinergic therapy for Alzheimer's disease. This review provides an updated view of the basal forebrain cholinergic system, its relation to cognition and its relevance for therapy of Alzheimer's disease. It deals with the three main aspects that form the basis of the cholinergic-oriented therapy of Alzheimer's disease, its origin, its mechanism of action, its clinical effects, advantages and limits of a cholinergic therapeutic approach. It includes a new and updated overview of the involvement of muscarinic receptors in Alzheimer's disease as well as the recent development of new and highly selective M1 muscarinic receptor agonists with disease-modifying potential. It also addresses the discovery of a novel nerve growth factor metabolic pathway responsible for the trophic maintenance of the basal forebrain system and its deregulation in Alzheimer's disease. It discusses new clinical studies and provides evidence for the long-term efficacy of cholinesterase inhibitor therapy suggesting a disease-modifying effect of these drugs. The classical symptomatic cholinergic therapy based on cholinesterase inhibitors is judiciously discussed for its maximal efficacy and best clinical application. The review proposes new alternatives of cholinergic therapy that should be developed to amplify its clinical effect and supplement the disease-modifying effect of new treatments to slow down or arrest disease progression.

摘要

目前,通过胆碱酯酶抑制剂增强胆碱能神经传递是治疗阿尔茨海默病早期和晚期认知和行为症状的主要可用方法。恢复胆碱能系统一直是改善阿尔茨海默病认知的主要手段,因为六种已批准的疗法中有四种是乙酰胆碱酯酶抑制剂。美金刚是一种 N-甲基-D-天冬氨酸拮抗剂,其对行为症状具有良好的临床疗效,通常与胆碱酯酶抑制剂联合使用以增强其疗效,而针对淀粉样蛋白病理的 aducanumab 最近也获得了批准。胆碱能系统的早期、进行性和选择性退化及其与认知缺陷的密切关系支持使用胆碱能疗法治疗阿尔茨海默病。本综述提供了对基底前脑胆碱能系统的最新观点,及其与认知的关系及其对阿尔茨海默病治疗的相关性。它涉及构成阿尔茨海默病胆碱能治疗基础的三个主要方面,即其起源、作用机制、临床效果、胆碱能治疗方法的优点和局限性。它包括对阿尔茨海默病中毒蕈碱受体参与的新的和更新的概述,以及具有疾病修饰潜力的新型和高度选择性 M1 毒蕈碱受体激动剂的最新发展。它还涉及到负责基底前脑系统营养维持的新的神经生长因子代谢途径的发现及其在阿尔茨海默病中的失调。它讨论了新的临床研究,并提供了胆碱酯酶抑制剂治疗的长期疗效证据,表明这些药物具有疾病修饰作用。基于胆碱酯酶抑制剂的经典对症胆碱能治疗被明智地讨论,以获得最大疗效并实现最佳临床应用。该综述提出了新的胆碱能治疗替代方案,应加以开发以增强其临床效果,并补充新疗法的疾病修饰作用,以减缓或阻止疾病进展。

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