Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD, USA.
Neuropsychopharmacology. 2018 Jan;43(1):103-115. doi: 10.1038/npp.2017.126. Epub 2017 Jun 27.
The endocannabinoid system (eCB) is implicated in the mediation of both reward and reinforcement. This is evidenced by the ability of exogenous cannabinoid drugs to produce hedonia and maintain self-administration in both human and animal subjects. eCBs similarly facilitate behaviors motivated by reward through interaction with the mesolimbic dopamine (DA) and endogenous opioid systems. Indeed, eCB signaling in the ventral tegmental area stimulates activation of midbrain DA cells and promotes DA release in terminal regions such as the nucleus accumbens (NAc). DA transmission mediates several aspects of reinforced behavior, such as motivation, incentive salience, and cost-benefit calculations. However, much research suggests that endogenous opioid signaling underlies the hedonic aspects of reward. eCBs and their receptors functionally interact with opioid systems within the NAc to support reward, most likely through augmenting DA release. This review explores the interaction of these systems as it relates to reward and reinforcement and examines current literature regarding their role in food reward.
内源性大麻素系统(eCB)在介导奖赏和强化方面起作用。这可以通过外源性大麻素药物产生快感和维持人类和动物被试的自我给药行为来证明。eCB 同样通过与中脑多巴胺(DA)和内源性阿片系统的相互作用促进受奖赏驱动的行为。事实上,腹侧被盖区的 eCB 信号刺激中脑 DA 细胞的激活,并促进终端区域(如伏隔核(NAc))中的 DA 释放。DA 传递介导强化行为的几个方面,如动机、激励显著性和成本效益计算。然而,大量研究表明,内源性阿片信号是奖赏快感方面的基础。eCB 及其受体在 NAc 内与阿片系统功能相互作用以支持奖赏,这很可能是通过增加 DA 释放。这篇综述探讨了这些系统之间的相互作用,以及它们与奖赏和强化的关系,并研究了它们在食物奖赏中的作用的当前文献。