Volpato Chiara, Schiff Sami, Facchini Silvia, Silvoni Stefano, Cavinato Marianna, Piccione Francesco, Antonini Angelo, Birbaumer Niels
Department of Behavioural Neuroscience, IRCCS Fondazione Ospedale San Camillo Venice, Italy.
Department of Medicine-DIMED, University of Padua Padua, Italy.
Front Behav Neurosci. 2016 Oct 24;10:205. doi: 10.3389/fnbeh.2016.00205. eCollection 2016.
Dopamine systems mediate key aspects of reward learning. Parkinson's disease (PD) represents a valuable model to study reward mechanisms because both the disease process and the anti-Parkinson medications influence dopamine neurotransmission. The aim of this pilot study was to investigate whether the level of levodopa differently modulates learning from positive and negative feedback and its electrophysiological correlate, the error related negativity (ERN), in PD. Ten PD patients and ten healthy participants performed a two-stage reinforcement learning task. In the Learning Phase, they had to learn the correct stimulus within a stimulus pair on the basis of a probabilistic positive or negative feedback. Three sets of stimulus pairs were used. In the Testing Phase, the participants were tested with novel combinations of the stimuli previously experienced to evaluate whether they learned more from positive or negative feedback. PD patients performed the task both ON- and OFF-levodopa in two separate sessions while they remained on stable therapy with dopamine agonists. The electroencephalogram (EEG) was recorded during the task. PD patients were less accurate in negative than positive learning both OFF- and ON-levodopa. In the OFF-levodopa state they were less accurate than controls in negative learning. PD patients had a smaller ERN amplitude OFF- than ON-levodopa only in negative learning. In the OFF-levodopa state they had a smaller ERN amplitude than controls in negative learning. We hypothesize that high tonic dopaminergic stimulation due to the dopamine agonist medication, combined to the low level of phasic dopamine due to the OFF-levodopa state, could prevent phasic "dopamine dips" indicated by the ERN needed for learning from negative feedback.
多巴胺系统介导奖赏学习的关键方面。帕金森病(PD)是研究奖赏机制的一个有价值的模型,因为疾病过程和抗帕金森药物都会影响多巴胺神经传递。这项初步研究的目的是调查左旋多巴水平是否以不同方式调节帕金森病患者从正性和负性反馈中学习的过程及其电生理相关指标——错误相关负波(ERN)。10名帕金森病患者和10名健康参与者进行了一项两阶段强化学习任务。在学习阶段,他们必须根据概率性的正性或负性反馈在一对刺激中学习正确的刺激。使用了三组刺激对。在测试阶段,参与者用之前经历过的刺激的新组合进行测试,以评估他们是否从正性或负性反馈中学到更多。帕金森病患者在两个单独的时段分别在服用和未服用左旋多巴的情况下完成任务,同时他们继续接受多巴胺激动剂的稳定治疗。在任务过程中记录脑电图(EEG)。帕金森病患者在未服用和服用左旋多巴时,负性学习的准确性均低于正性学习。在未服用左旋多巴状态下,他们在负性学习中的准确性低于对照组。仅在负性学习中,帕金森病患者未服用左旋多巴时的ERN波幅小于服用左旋多巴时。在未服用左旋多巴状态下,他们在负性学习中的ERN波幅小于对照组。我们推测,多巴胺激动剂药物引起的高张力多巴胺能刺激,加上未服用左旋多巴状态下的低水平相位多巴胺,可能会阻止从负性反馈中学习所需的由ERN指示的相位性“多巴胺下降”。