Department of Psychology, University of Oslo, Blindern, N Oslo, Norway.
Department of Diagnostic Physics, Oslo University Hospital, Nydalen, N Oslo, Norway.
Soc Cogn Affect Neurosci. 2019 May 17;14(4):411-422. doi: 10.1093/scan/nsz022.
The μ-opioid receptor (MOR) system has long been thought to underpin the rewarding properties of pleasant touch. Numerous non-human animal studies implicate MORs in social behaviours involving touch, but little is currently known about MOR involvement in human touch reward. Here, we employed a bi-directional pharmacological double-blind crossover design to assess the role of the human MOR system for touch pleasantness and motivation. Forty-nine male volunteers received 10 mg per-oral morphine, 50 mg per-oral naltrexone and placebo before being brushed on their forearm at three different velocities (0.3, 3 and 30 cm/s). In a touch liking task, pleasantness ratings were recorded after each 15 s brushing trial. In a touch wanting task, participants actively manipulated trial duration through key presses. As expected, 3 cm/s was the preferred velocity, producing significantly higher pleasantness ratings and wanting scores than the other stimuli. Contrary to our hypothesis, MOR drug manipulations did not significantly affect either touch pleasantness or wanting. The null effects were supported by post hoc Bayesian analyses indicating that the models with no drug effect were more than 25 times more likely than the alternative models given the data. We conclude that μ-opioid signalling is unlikely to underpin non-affiliative touch reward in humans.
μ-阿片受体(MOR)系统长期以来被认为是产生愉悦触感的基础。许多非人类动物研究表明,MOR 参与了涉及触摸的社交行为,但目前对于 MOR 在人类触摸奖励中的作用知之甚少。在这里,我们采用双向药理学双盲交叉设计来评估人类 MOR 系统在触摸愉悦感和动机方面的作用。49 名男性志愿者分别接受了 10 毫克口服吗啡、50 毫克口服纳曲酮和安慰剂,然后在前臂以三种不同的速度(0.3、3 和 30 厘米/秒)进行刷拭。在触摸喜好任务中,在每次 15 秒的刷拭试验后记录愉悦度评分。在触摸欲望任务中,参与者通过按键主动控制试验持续时间。正如预期的那样,3 厘米/秒是首选速度,产生的愉悦度评分和欲望评分明显高于其他刺激。与我们的假设相反,MOR 药物处理并没有显著影响触摸愉悦感或欲望。事后贝叶斯分析支持了无效效应,表明在给定数据的情况下,没有药物效应的模型比替代模型的可能性超过 25 倍。我们的结论是,μ-阿片信号不太可能是人类非亲和性触摸奖励的基础。