Donders Institute for Brain, Cognition and Behavior, Radboud University, Nijmegen 6500, the Netherlands; Department of Psychology, New York University, New York, NY 10003, USA.
Neuron. 2013 Nov 20;80(4):1090-100. doi: 10.1016/j.neuron.2013.08.030.
Serotonin and dopamine are speculated to subserve motivationally opponent functions, but this hypothesis has not been directly tested. We studied the role of these neurotransmitters in probabilistic reversal learning in nearly 700 individuals as a function of two polymorphisms in the genes encoding the serotonin and dopamine transporters (SERT: 5HTTLPR plus rs25531; DAT1 3'UTR VNTR). A double dissociation was observed. The SERT polymorphism altered behavioral adaptation after losses, with increased lose-shift associated with L' homozygosity, while leaving unaffected perseveration after reversal. In contrast, the DAT1 genotype affected the influence of prior choices on perseveration, while leaving lose-shifting unaltered. A model of reinforcement learning captured the dose-dependent effect of DAT1 genotype, such that an increasing number of 9R-alleles resulted in a stronger reliance on previous experience and therefore reluctance to update learned associations. These data provide direct evidence for doubly dissociable effects of serotonin and dopamine systems.
血清素和多巴胺被推测具有动机相反的功能,但这一假设尚未得到直接验证。我们研究了近 700 名个体中这些神经递质在概率反转学习中的作用,这是编码血清素和多巴胺转运蛋白(SERT:5HTTLPR 加 rs25531;DAT1 3'UTR VNTR)的基因的两个多态性的功能。观察到双重分离。SERT 多态性改变了损失后的行为适应,与 L' 纯合子相关的失移增加,而反转后不受影响的坚持。相比之下,DAT1 基因型影响先前选择对坚持的影响,而失移不变。强化学习模型捕获了 DAT1 基因型的剂量依赖性效应,即 9R-等位基因的数量增加导致对先前经验的更强依赖,因此不愿意更新已学习的关联。这些数据为血清素和多巴胺系统的双重可分离效应提供了直接证据。