Rangel College of Pharmacy, Texas A&M University, Kingsville, TX, 78363, USA.
Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT, 06269, USA.
Acta Pharmacol Sin. 2019 Mar;40(3):324-335. doi: 10.1038/s41401-018-0164-x. Epub 2018 Oct 17.
The cannabinoid type-1 (CB) receptor, a G-protein-coupled receptor, is an attractive target for drug discovery due to its involvement in many physiological processes. Historically, drug discovery efforts targeting the CB receptor have focused on the development of orthosteric ligands that interact with the active site to which endogenous cannabinoids bind. Research performed over the last several decades has revealed substantial difficulties in translating CB orthosteric ligands into druggable candidates. The difficulty is mainly due to the adverse effects associated with orthosteric CB ligands. Recent discoveries of allosteric CB modulators provide tremendous opportunities to develop CB ligands with novel mechanisms of action; these ligands may potentially improve the pharmacological effects and enhance drug safety in treating the disorders by regulating the functions of the CB receptor. In this paper, we review and summarize the complex pharmacological profiles of each class of CB allosteric modulators, the development of new classes of CB allosteric modulators and the results from in vivo assessments of their therapeutic value.
大麻素型 1(CB)受体是一种 G 蛋白偶联受体,由于其参与许多生理过程,因此成为药物发现的有吸引力的靶标。从历史上看,针对 CB 受体的药物发现工作主要集中在开发与内源性大麻素结合的活性部位相互作用的正位配体上。过去几十年的研究表明,将 CB 正位配体转化为可成药的候选物存在很大的困难。这种困难主要是由于与正位 CB 配体相关的不良反应。最近发现的变构 CB 调节剂为开发具有新型作用机制的 CB 配体提供了巨大的机会;这些配体通过调节 CB 受体的功能,可能潜在地改善治疗疾病的药理作用并提高药物安全性。本文综述和总结了每一类 CB 变构调节剂的复杂药理学特征、新型 CB 变构调节剂的开发以及它们在体内评估治疗价值的结果。