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大麻素在治疗帕金森病相关神经炎症中的治疗潜力。

Therapeutic potential of cannabinoids in the treatment of neuroinflammation associated with Parkinson's disease.

机构信息

Department of Biology, University of British Columbia Okanagan, Kelowna, BC, Canada.

出版信息

Mini Rev Med Chem. 2011 Jun;11(7):582-90. doi: 10.2174/138955711795906905.

Abstract

The cannabinoid system is represented by two principal receptor subtypes, termed CB1 and CB2, along with several endogenous ligands. In the central nervous system it is involved in several processes. CB1 receptors are mainly expressed by neurons and their activation is primarily implicated in psychotropic and motor effects of cannabinoids. CB2 receptors are expressed by glial cells and are thought to participate in regulation of neuroimmune reactions. This review aims to highlight several reported properties of cannabinoids that could be used to inhibit the adverse neuroinflammatory processes contributing to Parkinson's disease and possibly other neurodegenerative disorders. These include anti-oxidant properties of phytocannabinoids and synthetic cannabinoids as well as hypothermic and antipyretic effects. However, cannabinoids may also trigger signaling cascades leading to impaired mitochondrial enzyme activity, reduced mitochondrial biogenesis, and increased oxidative stress, all of which could contribute to neurotoxicity. Therefore, further pharmacological studies are needed to allow rational design of new cannabinoid-based drugs lacking detrimental in vivo effects.

摘要

大麻素系统由两种主要的受体亚型组成,分别称为 CB1 和 CB2,以及几种内源性配体。在中枢神经系统中,它参与了几个过程。CB1 受体主要由神经元表达,其激活主要与大麻素的精神作用和运动作用有关。CB2 受体由神经胶质细胞表达,被认为参与神经免疫反应的调节。本综述旨在强调大麻素的几种已报道的特性,这些特性可用于抑制导致帕金森病和可能其他神经退行性疾病的不良神经炎症过程。这些特性包括植物大麻素和合成大麻素的抗氧化特性,以及降温作用和退热作用。然而,大麻素也可能触发信号级联反应,导致线粒体酶活性受损、线粒体生物发生减少和氧化应激增加,所有这些都可能导致神经毒性。因此,需要进一步的药理学研究来允许合理设计新的基于大麻素的药物,而这些药物缺乏有害的体内作用。

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