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Opioid and cannabinoid receptors: friends with benefits or just close friends?

机译:阿片和大麻素受体:有益处的朋友还是只是亲密的朋友?

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摘要

μ-Opioid (MOP) and cannabinoid CB1 receptors mediate overlapping pharmacological responses in clinically important areas such as drug abuse and pain management, and functional interactions between agonists at these receptors have long been recognized. In the present issue of this Journal, Rios and co-workers have provided the first strong evidence that the two receptors interact directly when coexpressed in the same cells. The authors report a close physical association between MOP and CB1 receptors and novel pharmacological interactions of MOP and CB1 agonists. They argue that MOP/CB1 heterodimer formation explains these interactions. If correct, the direct interaction of MOP and CB1 pharmacophores in a quaternary complex would provide real benefits by opening the potential for development of novel MOP/CB1 small molecules or new strategies for use of current ligands. However, a lot more evidence will be required before the heterodimer interpretation can be accepted. If it turns out that MOP and CB1 receptors do not readily form hetero-oligomers, the study by Rios and co-workers shows that they are still friends but there may be few benefits.
机译:μ阿片类药物(MOP)和大麻素CB1受体在诸如药物滥用和疼痛管理等临床重要领域介导重叠的药理反应,并且早就认识到激动剂之间在这些受体上的功能相互作用。在本期杂志的最新一期中,Rios及其同事提供了第一个有力的证据,证明两种受体在同一细胞中共表达时会直接相互作用。作者报告了MOP和CB1受体之间的紧密物理联系以及MOP和CB1激动剂的新型药理相互作用。他们认为MOP / CB1异二聚体的形成解释了这些相互作用。如果正确,则通过打开开发新型MOP / CB1小分子或使用当前配体的新策略的潜力,MOP和CB1药效团在四元复合物中的直接相互作用将提供真正的好处。但是,在接受异二聚体解释之前,将需要更多的证据。如果事实证明MOP和CB1受体不易形成异源寡聚体,则Rios及其同事的研究表明,它们仍然是朋友,但可能没有什么好处。

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