Suppr超能文献

大麻素受体配体:与未来药物发现和开发相关的临床及神经药理学考量

Cannabinoid receptor ligands: clinical and neuropharmacological considerations, relevant to future drug discovery and development.

作者信息

Pertwee R G

机构信息

Department of Biomedical Sciences, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, Scotland.

出版信息

Expert Opin Investig Drugs. 2000 Jul;9(7):1553-71. doi: 10.1517/13543784.9.7.1553.

Abstract

This review highlights some important advances that have taken place in cannabinoid research over the last four years. It focuses on novel ligands that are of interest either as experimental tools or as lead compounds for therapeutic agents and possible clinical applications for some of these ligands. The molecular targets for these compounds are various components of the system of endogenous cannabinoids (endocannabinoids) and receptors that together constitute the 'endocannabinoid system'. These are CB(1) cannabinoid receptors that are present mainly on central and peripheral neurones, CB(2) cannabinoid receptors that are expressed predominantly by immune cells, the biochemical mechanisms responsible for the tissue uptake or metabolism of endocannabinoids and vanilloid receptors. Other cannabinoid receptor types may also exist. Recently developed ligands include potent and selective agonists for CB(1) and CB(2) receptors, a potent CB(2)-selective antagonist/inverse agonist and inhibitors of endocannabinoid uptake or metabolism. Future research should be directed at characterising the endocannabinoid system more completely and at obtaining more conclusive clinical data about the possible beneficial effects of cannabinoids as well as their adverse effects. There is also a need for improved cannabinoid formulations/modes of administration in the clinic and advances in this area should be facilitated by the recent development of a potent water-soluble CB(1)/CB(2) receptor agonist. A growing number of strategies for separating sought-after therapeutic effects of cannabinoid receptor agonists from the unwanted consequences of CB(1) receptor activation are now emerging and these are discussed at the end of this review.

摘要

本综述重点介绍了过去四年大麻素研究中取得的一些重要进展。它聚焦于作为实验工具或治疗药物先导化合物具有研究价值的新型配体,以及其中一些配体可能的临床应用。这些化合物的分子靶点是内源性大麻素(内源性大麻素)系统和受体的各种组成部分,它们共同构成了“内源性大麻素系统”。这些包括主要存在于中枢和外周神经元上的CB(1)大麻素受体、主要由免疫细胞表达的CB(2)大麻素受体、负责内源性大麻素组织摄取或代谢的生化机制以及香草酸受体。可能还存在其他类型的大麻素受体。最近开发的配体包括CB(1)和CB(2)受体的强效和选择性激动剂、强效CB(2)选择性拮抗剂/反向激动剂以及内源性大麻素摄取或代谢抑制剂。未来的研究应致力于更全面地表征内源性大麻素系统,并获得关于大麻素可能的有益作用及其不良反应的更确凿临床数据。临床上还需要改进大麻素制剂/给药方式,最近开发的一种强效水溶性CB(1)/CB(2)受体激动剂应能推动该领域的进展。现在出现了越来越多的策略,可将大麻素受体激动剂的理想治疗效果与CB(1)受体激活的不良后果区分开来,本综述结尾将对此进行讨论。

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