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新型 MAO-B 抑制剂:选择性 MAO-B 抑制剂 PF9601N 在帕金森病中的潜在治疗用途。

Novel MAO-B inhibitors: potential therapeutic use of the selective MAO-B inhibitor PF9601N in Parkinson's disease.

机构信息

Institut de Neurociències and Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Cerdanyola del Vallès (Barcelona), Spain.

出版信息

Int Rev Neurobiol. 2011;100:217-36. doi: 10.1016/B978-0-12-386467-3.00011-X.

Abstract

Parkinson's disease (PD) is a neurodegenerative disease that is characterized by preferential loss of dopaminergic neurons in the substantia nigra pars compacta, leading to declining levels of dopamine in the striatum. In our search for compounds able not only to extend the effects of dopamine by preventing its degradation but also to halt or slow the neurodegenerative process, we designed, synthesized, and biologically tested a series of propargylamines for their potential use as therapeutic agents for PD. Among them, PF9601N, [N-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine], showed high potency and selectivity as a MAO-BI (monoamine oxidase type B inhibitor) and also demonstrated remarkable neuroprotective properties in several in vivo and cellular models of PD. In this chapter, we describe the preclinical evidence revealing the novel MAO-BI PF9601N as an interesting candidate for the treatment of PD.

摘要

帕金森病(PD)是一种神经退行性疾病,其特征是黑质致密部多巴胺能神经元的优先丧失,导致纹状体中多巴胺水平下降。在寻找不仅能通过防止多巴胺降解来延长其作用,而且能阻止或减缓神经退行性过程的化合物的过程中,我们设计、合成并对一系列炔丙胺进行了生物学测试,以评估其作为 PD 治疗剂的潜力。其中,PF9601N[(2-丙炔基)-2-(5-苄氧基-吲哚基)甲胺]作为 MAO-BI(单胺氧化酶 B 抑制剂)表现出高活性和选择性,并且在 PD 的几种体内和细胞模型中显示出显著的神经保护特性。在本章中,我们描述了临床前证据,揭示了新型 MAO-BI PF9601N 作为治疗 PD 的一个有趣候选药物。

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