Department of Psychology, Emory University, Atlanta, GA, USA.
Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
Nat Hum Behav. 2023 Aug;7(8):1332-1343. doi: 10.1038/s41562-023-01639-0. Epub 2023 Jun 29.
Pleasure is a fundamental driver of human behaviour, yet its neural basis remains largely unknown. Rodent studies highlight opioidergic neural circuits connecting the nucleus accumbens, ventral pallidum, insula and orbitofrontal cortex as critical for the initiation and regulation of pleasure, and human neuroimaging studies exhibit some translational parity. However, whether activation in these regions conveys a generalizable representation of pleasure regulated by opioidergic mechanisms remains unclear. Here we use pattern recognition techniques to develop a human functional magnetic resonance imaging signature of mesocorticolimbic activity unique to states of pleasure. In independent validation tests, this signature is sensitive to pleasant tastes and affect evoked by humour. The signature is spatially co-extensive with mu-opioid receptor gene expression, and its response is attenuated by the opioid antagonist naloxone. These findings provide evidence for a basis of pleasure in humans that is distributed across brain systems.
愉悦是人类行为的基本驱动力,但它的神经基础在很大程度上仍然未知。啮齿动物研究强调了阿片能神经回路,这些神经回路连接伏隔核、腹侧苍白球、脑岛和眶额皮质,对于愉悦的产生和调节至关重要,人类神经影像学研究也表现出一定的转化一致性。然而,这些区域的激活是否传递了一种由阿片机制调节的可普遍化的愉悦表达仍然不清楚。在这里,我们使用模式识别技术来开发一种人类功能磁共振成像的特征,该特征是中脑边缘多巴胺能活动所特有的愉悦状态。在独立的验证测试中,这个特征对愉快的味道和幽默引起的情感是敏感的。该特征在空间上与μ-阿片受体基因表达一致,其反应被阿片拮抗剂纳洛酮所减弱。这些发现为人类愉悦的基础提供了证据,这个基础分布在大脑系统中。