Synthetic Cannabinoid Receptor Agonists and Antagonists: Implication in CNS Disorders.

Clementina Manera, Chiara Arena, Andrea Chicca
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引用次数: 7

Abstract

Background: Since the discovery of the cannabinoid receptors, numerous studies associate the endocannabinoid system with several physiological and pathological processes including cancer, appetite, fertility, memory, neuropathic and inflammatory pain, obesity, and neurodegenerative diseases. Over the last two decades, several researches have been dedicated extensively on the cannabinoid receptors ligands since the direct activation of cannabinoid receptors results in several beneficial effects, in the brain and in the periphery. The cannabinoid CB1 and CB2 receptor synthetic ligands reported in this review have been collected by a wide research of scientific literature in particular in public database for patents and clinical trials. The references for patent numbers, clinical trial registry numbers, websites and scientific articles are reported in the reference section.

Results: During past years, cannabinoid CB1 and CB2 receptor ligands from plants or lab were rapidly developed and then various new structures were reported to be cannabinoids. However the CB1 receptor ligands have had a limited usefulness due to their psychotropic effects, dependence, and cognitive impairment. On the contrary the development of CB2 receptor ligands has been more productive. Furthermore peripherally restricted agonists as well as CB1 receptor positive or negative allosteric modulators were studied with the aim of eliminating the undesirable CB1 receptor central effects.

Conclusions: The CB1 and CB2 receptor ligands offer several therapeutic opportunities for several CNS-related diseases. Based on the scientific literature, this review provides an overview of CB1 and CB2 receptor synthetic ligands obtained from drug research and in particular those synthesized for therapeutic purposes and potential clinical applications for central nervous system disorders.

合成大麻素受体激动剂和拮抗剂:对中枢神经系统疾病的影响。
背景:自从大麻素受体被发现以来,许多研究将内源性大麻素系统与多种生理和病理过程联系起来,包括癌症、食欲、生育、记忆、神经性和炎症性疼痛、肥胖和神经退行性疾病。在过去的二十年中,由于大麻素受体的直接激活在大脑和外周产生了几种有益的作用,因此对大麻素受体配体进行了广泛的研究。本文报道的大麻素CB1和CB2受体合成配体是通过广泛的科学文献研究,特别是在专利和临床试验的公共数据库中收集到的。专利号、临床试验注册号、网站和科学文章的参考文献在参考文献部分报告。结果:近年来,大麻素CB1和CB2受体配体在植物和实验室中迅速发展,并报道了各种新结构的大麻素。然而,由于其精神药物作用、依赖性和认知障碍,CB1受体配体的有用性有限。相反,CB2受体配体的开发更富有成效。此外,研究了外周限制性激动剂以及CB1受体阳性或阴性变构调节剂,目的是消除不良的CB1受体中枢效应。结论:CB1和CB2受体配体为几种中枢相关疾病提供了治疗机会。本文基于科学文献,综述了从药物研究中获得的CB1和CB2受体合成配体,特别是用于中枢神经系统疾病的治疗目的和潜在临床应用的合成配体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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