Department of Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Elife. 2018 Nov 16;7:e39648. doi: 10.7554/eLife.39648.
It has been hypothesized that the pleasure of a reward in humans is mediated by an opioidergic system involving the hypothalamus, nucleus accumbens and the amygdala. Importantly, enjoying the pleasure of a reward is distinct from incentive salience induced by cues predicting the reward. We investigated this issue using a within subject, pharmacological challenge design with the opioid receptor antagonist naloxone and fMRI. Our data show that blocking opioid receptors reduced pleasure associated with viewing erotic pictures more than viewing symbols of reward such as money. This was paralleled by a reduction of activation in the ventral striatum, lateral orbitofrontal cortex, amygdala, hypothalamus and medial prefrontal cortex. Crucially, the naloxone induced activation decrease was observed at reward delivery, but not during reward anticipation, indicating that blocking opioid receptors decreases the pleasure of rewards in humans.
This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).
据推测,人类对奖励的快感是由涉及下丘脑、伏隔核和杏仁核的阿片能系统介导的。重要的是,享受奖励的快感与由预测奖励的线索引起的激励性显著不同。我们使用内源性药物挑战设计,结合阿片受体拮抗剂纳洛酮和 fMRI 研究了这个问题。我们的数据表明,阻断阿片受体减少了观看色情图片带来的快感,比观看金钱等奖励符号带来的快感更多。这与腹侧纹状体、外侧眶额皮质、杏仁核、下丘脑和内侧前额皮质的激活减少相平行。至关重要的是,纳洛酮诱导的激活减少是在奖励传递时观察到的,而不是在奖励预期时观察到的,这表明阻断阿片受体可降低人类对奖励的快感。
本文经过编辑处理,作者决定如何回应同行评审过程中提出的问题。审稿人的评估是所有问题都已得到解决(见评审意见信)。