Suppr超能文献

雷沙吉兰:一种新型具有神经保护活性的抗帕金森单胺氧化酶-B 抑制剂。

Rasagiline: a novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity.

机构信息

Eve Topf Centre of Excellence for Neurodegenerative Diseases, Technion-Rappaport Faculty of Medicine, Efron St. PO Box 9697, Haifa 31096, Israel.

出版信息

Prog Neurobiol. 2010 Nov;92(3):330-44. doi: 10.1016/j.pneurobio.2010.06.008. Epub 2010 Jun 19.

Abstract

Rasagiline (N-propargyl-1-(R)-aminoindan) is a novel, highly potent irreversible monoamine oxidase (MAO)-B inhibitor, anti-Parkinsonian drug. Rasagiline is effective as monotherapy or adjunct to L-Dopa for patients with early and late Parkinson's disease (PD). Its S-isomer, TVP1022 is thousand times less potent as an MAO-B inhibitor. However, both compounds have similar molecular mechanisms of neuroprotection in neuronal cell cultures and animal neurodegenerative models, indicating that the neuroprotective effect of rasagiline does not depend on inhibition of MAO-B, but rather is associated with the N-propargyl moiety, which promotes mitochondrial viability and stabilizes permeability transition by regulating Bcl-2 family proteins. Novel findings demonstrated that the major metabolite of rasagiline, 1-(R)-aminoindan has antioxidant and neuroprotective capabilities and thus, may contribute to the overt activity of its parent compound, rasagiline. This paper will review the earlier and present studies in the development of rasagiline for treatment of PD and discuss its pharmacology and applicable mechanism of action.

摘要

雷沙吉兰(N-丙炔基-1-(R)-氨基茚满)是一种新型、高效的单胺氧化酶(MAO)-B 抑制剂,抗帕金森病药物。雷沙吉兰可作为单独治疗药物或与左旋多巴联合治疗早期和晚期帕金森病(PD)患者。其 S-异构体 TVP1022 作为 MAO-B 抑制剂的效力低 1000 倍。然而,这两种化合物在神经元细胞培养物和动物神经退行性模型中具有相似的分子神经保护机制,表明雷沙吉兰的神经保护作用不依赖于 MAO-B 的抑制,而是与 N-丙炔基部分相关,该部分通过调节 Bcl-2 家族蛋白促进线粒体活力并稳定通透性转变。新的发现表明,雷沙吉兰的主要代谢物 1-(R)-氨基茚满具有抗氧化和神经保护能力,因此可能有助于其母体化合物雷沙吉兰的明显活性。本文将回顾雷沙吉兰治疗 PD 的早期和目前的研究,并讨论其药理学和适用的作用机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验