Geffe Sarah, Schindlbeck Katharina A, Mehl Arne, Jende Johann, Klostermann Fabian, Marzinzik Frank
Department of Neurology, Charité, University Medicine Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, 12203, Berlin, Germany.
Department of Neuroradiology, University Hospital Heidelberg, Heidelberg, Germany.
J Neural Transm (Vienna). 2016 Jun;123(6):601-10. doi: 10.1007/s00702-016-1557-y. Epub 2016 Apr 23.
Although dopamine is known to aggravate implicit learning, the exact impact on behaviour when feedback is unavailable remains unclear. Previous studies revealed that non-rewarded learning habits are affected in long-term dopaminergic treated patients with Parkinson's disease (PD). We studied the influence of a onetime levodopa intake on implicit learning in de novo, untreated PD patients. De novo PD patients (n = 22) before and after the single intake of levodopa and control subjects (n = 23) took part in a Go/NoGo paradigm. One stimulus was defined as target, which was first consistently preceded by one of three non-target stimuli (conditioning). This coupling was dissolved thereafter (deconditioning). In the 'Go version' subjects were asked to respond to the target by pressing a key, whereas in the 'NoGo version' response had to be inhibited. PD patients and controls (n = 14/n = 19) with an initial learning effect due to the target were included for further statistical analysis. Within the subgroup incorrect responses upon NoGo stimuli increased during the deconditioning phase. In contrast, the same patients failed to show any change after receiving 200 mg of levodopa. During the Go version, no change of the overall error rate between conditioning and deconditioning was detectable over all groups. Learning behaviour in untreated PD patients and healthy controls was indistinguishable. In contrast, the same patients varied in their implicit learning after one-time intake of levodopa, when actions had to be inhibited. Hence, the single intake of levodopa appears to modulate implicit learning behaviour in de novo PD patients.
尽管已知多巴胺会加重内隐学习,但在无法获得反馈时对行为的确切影响仍不清楚。先前的研究表明,长期接受多巴胺能治疗的帕金森病(PD)患者的无奖励学习习惯会受到影响。我们研究了一次左旋多巴摄入对初发、未治疗的PD患者内隐学习的影响。初发PD患者(n = 22)在单次摄入左旋多巴前后以及对照组(n = 23)参与了一个Go/NoGo范式。一种刺激被定义为目标刺激,它最初始终由三种非目标刺激之一作为先导(条件作用)。此后这种配对被解除(去条件作用)。在“Go版本”中,要求受试者通过按键对目标刺激做出反应,而在“NoGo版本”中则必须抑制反应。对因目标刺激而产生初始学习效应的PD患者和对照组(n = 14/n = 19)进行进一步的统计分析。在亚组中,NoGo刺激时的错误反应在去条件作用阶段增加。相比之下,同一组患者在接受200mg左旋多巴后未显示出任何变化。在Go版本中,所有组在条件作用和去条件作用之间的总体错误率均未检测到变化。未治疗的PD患者和健康对照组的学习行为没有差异。相比之下,同一组患者在单次摄入左旋多巴后,当必须抑制行动时,其内隐学习有所不同。因此,单次摄入左旋多巴似乎会调节初发PD患者的内隐学习行为。