Stopper Colin M, Floresco Stan B
Department of Psychology and Brain Research Centre, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Department of Psychology and Brain Research Centre, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada
Schizophr Bull. 2015 Jan;41(1):9-14. doi: 10.1093/schbul/sbu165. Epub 2014 Nov 17.
Abnormal reinforcement learning and representations of reward value are present in schizophrenia, and these impairments can manifest as deficits in risk/reward decision making. These abnormalities may be due in part to dopaminergic dysfunction within cortico-limbic-striatal circuitry. Evidence from studies with laboratory animal have revealed that normal DA activity within different nodes of these circuits is critical for mediating dissociable processes that can refine decision biases. Moreover, both phasic and tonic dopamine transmission appear to play separate yet complementary roles in these processes. Tonic dopamine release within the prefrontal cortex and nucleus accumbens, serves as a "running rate-meter" of reward and reflects contextual information such as reward uncertainty and overt choice behavior. On the other hand, manipulations of outcome-related phasic dopamine bursts and dips suggest these signals provide rapid feedback to allow for quick adjustments in choice as reward contingencies change. The lateral habenula is a key input to the DA system that phasic signals is necessary for expressing subjective decision biases; as suppression of activity within this nucleus leads to catastrophic impairments in decision making and random patterns of choice behavior. As schizophrenia is characterized by impairments in using positive and negative feedback to appropriately guide decision making, these findings suggest that these deficits in these processes may be mediated, at least in part, by abnormalities in both tonic and phasic dopamine transmission.
精神分裂症患者存在异常的强化学习和奖励价值表征,这些损害可表现为风险/奖励决策缺陷。这些异常可能部分归因于皮质-边缘-纹状体回路中的多巴胺能功能障碍。来自实验动物研究的证据表明,这些回路不同节点内的正常多巴胺活动对于介导可细化决策偏差的可分离过程至关重要。此外,多巴胺的相位性和紧张性传递在这些过程中似乎发挥着各自但互补的作用。前额叶皮质和伏隔核内的紧张性多巴胺释放充当奖励的“运行速率计”,并反映诸如奖励不确定性和公开选择行为等情境信息。另一方面,对与结果相关的相位性多巴胺爆发和下降的操纵表明,这些信号提供快速反馈,以便在奖励意外情况变化时快速调整选择。外侧缰核是多巴胺系统的关键输入,相位性信号对于表达主观决策偏差是必要的;因为抑制该核内的活动会导致决策灾难性损害和随机选择行为模式。由于精神分裂症的特征是在使用正性和负性反馈来适当指导决策方面存在损害,这些发现表明,这些过程中的这些缺陷可能至少部分由紧张性和相位性多巴胺传递异常介导。