• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/j.pneurobio.2010.06.008
PMID:20600573
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。

相似文献

1
Rasagiline: a novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity.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。
Prog Neurobiol. 2010 Nov;92(3):330-44. doi: 10.1016/j.pneurobio.2010.06.008. Epub 2010 Jun 19.
2
Mechanism of neuroprotective action of the anti-Parkinson drug rasagiline and its derivatives.抗帕金森病药物雷沙吉兰及其衍生物的神经保护作用机制。
Brain Res Brain Res Rev. 2005 Apr;48(2):379-87. doi: 10.1016/j.brainresrev.2004.12.027.
3
Comprehensive review of rasagiline, a second-generation monoamine oxidase inhibitor, for the treatment of Parkinson's disease.第二代单胺氧化酶抑制剂雷沙吉兰治疗帕金森病的综合综述。
Clin Ther. 2007 Sep;29(9):1825-49. doi: 10.1016/j.clinthera.2007.09.021.
4
Rasagiline: neurodegeneration, neuroprotection, and mitochondrial permeability transition.雷沙吉兰:神经退行性变、神经保护及线粒体通透性转换
J Neurosci Res. 2005;79(1-2):172-9. doi: 10.1002/jnr.20350.
5
The neuroprotective mechanism of 1-(R)-aminoindan, the major metabolite of the anti-parkinsonian drug rasagiline.1-(R)-氨基茚满,抗帕金森病药物雷沙吉兰的主要代谢产物的神经保护机制。
J Neurochem. 2010 Mar;112(5):1131-7. doi: 10.1111/j.1471-4159.2009.06542.x. Epub 2009 Dec 10.
6
Rasagiline (TVP-1012): a new selective monoamine oxidase inhibitor for Parkinson's disease.雷沙吉兰(TVP - 1012):一种用于帕金森病的新型选择性单胺氧化酶抑制剂。
Am J Geriatr Pharmacother. 2006 Dec;4(4):330-46. doi: 10.1016/j.amjopharm.2006.12.001.
7
Recent advances in Parkinson's disease therapy: use of monoamine oxidase inhibitors.帕金森病治疗的最新进展:单胺氧化酶抑制剂的应用
Expert Rev Neurother. 2005 Nov;5(6):811-21. doi: 10.1586/14737175.5.6.811.
8
Neuroprotective profile of the multitarget drug rasagiline in Parkinson's disease.治疗帕金森病的多靶点药物雷沙吉兰的神经保护作用。
Int Rev Neurobiol. 2011;100:127-49. doi: 10.1016/B978-0-12-386467-3.00007-8.
9
Bifunctional drug derivatives of MAO-B inhibitor rasagiline and iron chelator VK-28 as a more effective approach to treatment of brain ageing and ageing neurodegenerative diseases.单胺氧化酶-B抑制剂雷沙吉兰和铁螯合剂VK-28的双功能药物衍生物,作为治疗脑老化和老化神经退行性疾病的更有效方法。
Mech Ageing Dev. 2005 Feb;126(2):317-26. doi: 10.1016/j.mad.2004.08.023.
10
Monamine oxidase inhibitors: current and emerging agents for Parkinson disease.单胺氧化酶抑制剂:帕金森病的现有及新型药物
Clin Neuropharmacol. 2007 May-Jun;30(3):150-68. doi: 10.1097/01.wnf.0000240956.49315.be.

引用本文的文献

1
Rasagiline Inhibits Human Melanoma Cell Viability and Interacts Synergistically with Mitoxantrone and Antagonistically with Cisplatin-In Vitro Isobolographic Studies.雷沙吉兰抑制人黑色素瘤细胞活力,并与米托蒽醌协同作用、与顺铂拮抗作用——体外等效线图研究
Cancers (Basel). 2025 Aug 3;17(15):2563. doi: 10.3390/cancers17152563.
2
Streamlined analytical strategy using resonance Rayleigh scattering signal amplification for nanoscale quantification of rasagiline in tablets with content assessment.采用共振瑞利散射信号放大的简化分析策略用于片剂中雷沙吉兰的纳米级定量及含量评估。
BMC Chem. 2025 Jul 26;19(1):225. doi: 10.1186/s13065-025-01585-0.
3
Neuroprotection in Parkinson Disease.
帕金森病中的神经保护
Neurol Ther. 2025 Jul 18. doi: 10.1007/s40120-025-00793-z.
4
Inhibitory Activity of - and -Functionalized Monoterpene Diols Towards Monoamine Oxidases A and B.α-和β-官能化单萜二醇对单胺氧化酶A和B的抑制活性
Int J Mol Sci. 2024 Dec 26;26(1):97. doi: 10.3390/ijms26010097.
5
Prominent Neuroprotective Potential of Indole-2--methylpropargylamine: High Affinity and Irreversible Inhibition Efficiency towards Monoamine Oxidase B Revealed by Computational Scaffold Analysis.吲哚 - 2 - 甲基炔丙胺显著的神经保护潜力:通过计算支架分析揭示其对单胺氧化酶B的高亲和力和不可逆抑制效率
Pharmaceuticals (Basel). 2024 Sep 28;17(10):1292. doi: 10.3390/ph17101292.
6
FeO/PANI/CuI as a sustainable heterogeneous nanocatalyst for A coupling.FeO/PANI/CuI作为用于A偶联反应的可持续多相纳米催化剂。
Nanoscale Adv. 2024 Jul 22;6(19):4842-4851. doi: 10.1039/d4na00448e. eCollection 2024 Sep 24.
7
Melanin-The Éminence Grise of Melanoma and Parkinson's Disease Development.黑色素——黑色素瘤和帕金森病发展中的幕后关键因素
Cancers (Basel). 2023 Nov 23;15(23):5541. doi: 10.3390/cancers15235541.
8
A sporadic Parkinson's disease model via silencing of the ubiquitin-proteasome/E3 ligase component, SKP1A.通过沉默泛素-蛋白酶体/E3 连接酶组件 SKP1A 建立散发性帕金森病模型。
J Neural Transm (Vienna). 2024 Jun;131(6):675-707. doi: 10.1007/s00702-023-02687-6. Epub 2023 Aug 29.
9
Nanotechnology-empowered therapeutics targeting neurodegenerative diseases.纳米技术赋能的神经退行性疾病治疗策略。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2023 Sep-Oct;15(5):e1907. doi: 10.1002/wnan.1907. Epub 2023 May 30.
10
Current Pharmacotherapy and Multi-Target Approaches for Alzheimer's Disease.阿尔茨海默病的当前药物治疗与多靶点治疗方法
Pharmaceuticals (Basel). 2022 Dec 14;15(12):1560. doi: 10.3390/ph15121560.