Suppr超能文献

转运蛋白配体有望成为治疗焦虑症的有效工具。

Translocator protein ligands as promising therapeutic tools for anxiety disorders.

作者信息

Taliani S, Da Settimo F, Da Pozzo E, Chelli B, Martini C

机构信息

Department of Pharmaceutical Science, University of Pisa, Italy.

出版信息

Curr Med Chem. 2009;16(26):3359-80. doi: 10.2174/092986709789057653. Epub 2009 Sep 1.

Abstract

The Translocator protein (TSPO), formerly known as the peripheral-type benzodiazepine receptor, is an 18 kDa mitochondrial protein primarily involved in steroid biosynthesis in both peripheral and glial cells. It has been extensively reported that TSPO regulates the rate-limiting translocation of cholesterol from the outer to the inner mitochondrial membrane before its transformation by cytochrome P450(scc) into pregnenolone, which is further converted into an array of different steroids. In the brain, neurosteroids such as allopregnanolone and pregnenolone, acting as positive modulators of gamma-aminobutyric type A (GABA(A)) receptors, exert anxiolytic activity. Specific ligands targeting TSPO increase neurosteroid production and for this reason they have been suggested to play an important role in anxiety modulation. Unlike benzodiazepines (Bzs), which represent the most common anti-anxiety drugs administered around the world, selective TSPO ligands have shown anxiolytic effects in animal models without any of the side effects associated with Bzs. Therefore, specific TSPO ligands that are able to promote neurosteroidogenesis may represent the future of therapeutic treatment of anxiety disorders. Furthermore, TSPO expression levels are altered in several different psychiatric disorders in which anxiety is the main symptom. This article reviews the primary and patent literature over the last decade concerning the development of novel TSPO ligands that have resulted effective in various models of anxiety, taking into special consideration their structure-activity relationships.

摘要

转位蛋白(TSPO),以前称为外周型苯二氮䓬受体,是一种18 kDa的线粒体蛋白,主要参与外周细胞和神经胶质细胞中的类固醇生物合成。已有大量报道称,TSPO在胆固醇被细胞色素P450(scc)转化为孕烯醇酮之前,调节胆固醇从线粒体外膜到内膜的限速转位,孕烯醇酮进一步转化为一系列不同的类固醇。在大脑中,诸如别孕烯醇酮和孕烯醇酮等神经类固醇作为γ-氨基丁酸A型(GABAA)受体的正向调节剂,发挥抗焦虑活性。靶向TSPO的特异性配体可增加神经类固醇的产生,因此它们被认为在焦虑调节中起重要作用。与作为全球最常用抗焦虑药物的苯二氮䓬类药物不同,选择性TSPO配体在动物模型中显示出抗焦虑作用,且没有任何与苯二氮䓬类药物相关的副作用。因此,能够促进神经类固醇生成的特异性TSPO配体可能代表焦虑症治疗的未来。此外,在以焦虑为主要症状的几种不同精神疾病中,TSPO表达水平会发生改变。本文回顾了过去十年中有关新型TSPO配体开发的主要文献和专利文献,这些配体在各种焦虑模型中均已证明有效,并特别考虑了它们的构效关系。

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