Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Braga 4710-057, Portugal.
ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães 4710-057, Portugal.
Nat Commun. 2016 Jun 23;7:11829. doi: 10.1038/ncomms11829.
Striatal dopamine receptor D1-expressing neurons have been classically associated with positive reinforcement and reward, whereas D2 neurons are associated with negative reinforcement and aversion. Here we demonstrate that the pattern of activation of D1 and D2 neurons in the nucleus accumbens (NAc) predicts motivational drive, and that optogenetic activation of either neuronal population enhances motivation in mice. Using a different approach in rats, we further show that activating NAc D2 neurons increases cue-induced motivational drive in control animals and in a model that presents anhedonia and motivational deficits; conversely, optogenetic inhibition of D2 neurons decreases motivation. Our results suggest that the classic view of D1-D2 functional antagonism does not hold true for all dimensions of reward-related behaviours, and that D2 neurons may play a more prominent pro-motivation role than originally anticipated.
纹状体多巴胺受体 D1 表达神经元与正强化和奖励有关,而 D2 神经元与负强化和厌恶有关。在这里,我们证明了伏隔核(NAc)中 D1 和 D2 神经元的激活模式可以预测动机驱动,并且光遗传学激活这两种神经元群都可以增强小鼠的动机。在大鼠中使用不同的方法,我们进一步表明,激活 NAc D2 神经元会增加对照动物和表现出快感缺失和动机缺陷的模型中的线索诱导动机驱动;相反,光遗传学抑制 D2 神经元会降低动机。我们的结果表明,D1-D2 功能拮抗的经典观点并不适用于所有与奖励相关行为的维度,并且 D2 神经元可能比最初预期的发挥更突出的促进动机作用。