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M1 激动剂作为阿尔茨海默病潜在的疾病修饰疗法。

M1 agonists as a potential disease-modifying therapy for Alzheimer's disease.

作者信息

Caccamo Antonella, Fisher Abraham, LaFerla Frank M

机构信息

Department of Neurobiology, University of California, Irvine, Irvine, CA 92697, USA.

出版信息

Curr Alzheimer Res. 2009 Apr;6(2):112-7. doi: 10.2174/156720509787602915.

Abstract

Cholinergic deficit is a cardinal feature of Alzheimer's disease, and cholinesterase inhibitors represent one of the most prominent means of mitigating this dysfunction. Cholinesterase inhibitors provide mild symptomatic relief, although they lose their efficacy over time most likely because they are not disease-modifying agents. An alternative strategy for restoring cholinergic function and attenuating the cognitive decline involves acting on the receptors on which acetylcholine acts. Stimulation of muscarinic acetylcholine receptors and in particular the M1 subtype has been shown to have a beneficial effect in restoring cognition in patients with Alzheimer's disease and in attenuating Abeta and tau pathology in different animal models. In this review, we discuss the role of M1 agonists as a potential disease-modifying therapy for Alzheimer's disease.

摘要

胆碱能缺陷是阿尔茨海默病的主要特征,胆碱酯酶抑制剂是缓解这种功能障碍的最主要手段之一。胆碱酯酶抑制剂能提供轻微的症状缓解,尽管随着时间推移它们会失去疗效,这很可能是因为它们不是疾病修饰药物。恢复胆碱能功能并减轻认知衰退的另一种策略是作用于乙酰胆碱作用的受体。已表明刺激毒蕈碱型乙酰胆碱受体,尤其是M1亚型,对恢复阿尔茨海默病患者的认知以及减轻不同动物模型中的β淀粉样蛋白和tau蛋白病理改变具有有益作用。在本综述中,我们讨论了M1激动剂作为阿尔茨海默病潜在疾病修饰疗法的作用。

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