Physiologie de la Reproduction et des Comportements, INRA UMR-0085, CNRS UMR-7247, Université de Tours Rabelais, IFCE, Inserm, Nouzilly, France.
Br J Pharmacol. 2018 Jul;175(14):2750-2769. doi: 10.1111/bph.13808. Epub 2017 May 4.
The endogenous opioid system is well known to relieve pain and underpin the rewarding properties of most drugs of abuse. Among opioid receptors, the μ receptor mediates most of the analgesic and rewarding properties of opioids. Based on striking similarities between social distress, physical pain and opiate withdrawal, μ receptors have been proposed to play a critical role in modulating social behaviour in humans and animals. This review summarizes experimental data demonstrating such role and proposes a novel model, the μ opioid receptor balance model, to account for the contribution of μ receptors to the subtle regulation of social behaviour. Interestingly, μ receptor null mice show behavioural deficits similar to those observed in patients with autism spectrum disorder (ASD), including severe impairment in social interactions. Therefore, after a brief summary of recent evidence for blunted (social) reward processes in subjects with ASD, we review here arguments for altered μ receptor function in this pathology. This article is part of a themed section on Emerging Areas of Opioid Pharmacology. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.14/issuetoc.
内源性阿片系统是众所周知的缓解疼痛和支持大多数药物滥用的奖励属性。在阿片受体中,μ受体介导阿片类药物的大部分镇痛和奖励特性。基于社会痛苦,身体疼痛和阿片类药物戒断之间的惊人相似性,μ受体被认为在调节人类和动物的社会行为方面发挥着关键作用。这篇综述总结了实验数据,证明了这种作用,并提出了一个新的模型,即μ阿片受体平衡模型,以解释μ受体对社会行为的微妙调节的贡献。有趣的是,μ受体缺失小鼠表现出与自闭症谱系障碍(ASD)患者相似的行为缺陷,包括严重的社交互动障碍。因此,在简要总结了 ASD 患者中(社交)奖励过程迟钝的最新证据后,我们在此回顾了该病理中μ受体功能改变的论据。本文是阿片类药物药理学新兴领域专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.14/issuetoc.