The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
Neuropsychopharmacology. 2023 Dec;48(13):1849-1858. doi: 10.1038/s41386-023-01615-2. Epub 2023 Jun 3.
Catecholamine-enhancing psychostimulants, such as methylphenidate have long been argued to undermine creative thinking. However, prior evidence for this is weak or contradictory, stemming from studies with small sample sizes that do not consider the well-established large variability in psychostimulant effects across different individuals and task demands. We aimed to definitively establish the link between psychostimulants and creative thinking by measuring effects of methylphenidate in 90 healthy participants on distinct creative tasks that measure convergent and divergent thinking, as a function of individuals' baseline dopamine synthesis capacity, indexed with F-FDOPA PET imaging. In a double-blind, within-subject design, participants were administered methylphenidate, placebo or selective D2 receptor antagonist sulpiride. The results showed that striatal dopamine synthesis capacity and/or methylphenidate administration did not affect divergent and convergent thinking. However, exploratory analysis demonstrated a baseline dopamine-dependent effect of methylphenidate on a measure of response divergence, a creativity measure that measures response variability. Response divergence was reduced by methylphenidate in participants with low dopamine synthesis capacity but enhanced in those with high dopamine synthesis capacity. No evidence of any effect of sulpiride was found. These results show that methylphenidate can undermine certain forms of divergent creativity but only in individuals with low baseline dopamine levels.
儿茶酚胺增强型精神兴奋剂,如哌甲酯,长期以来一直被认为会破坏创造性思维。然而,这方面的证据之前很薄弱或相互矛盾,源于样本量小的研究,这些研究没有考虑到不同个体和任务需求之间已经确立的精神兴奋剂效应的巨大可变性。我们旨在通过使用正电子发射断层扫描成像(PET)测量 90 名健康参与者的基础多巴胺合成能力,来确定哌甲酯与创造性思维之间的联系,这些参与者接受了不同的创造性任务,以衡量聚合思维和发散思维,这些任务衡量了集中和发散思维。在一项双盲、自身对照的设计中,参与者接受了哌甲酯、安慰剂或选择性 D2 受体拮抗剂舒必利的治疗。结果表明,纹状体多巴胺合成能力和/或哌甲酯的给药并不影响发散思维和聚合思维。然而,探索性分析表明,在一项衡量反应发散性的创造力衡量标准中,存在一种与基线多巴胺有关的哌甲酯的作用,该衡量标准衡量反应的可变性。在多巴胺合成能力较低的参与者中,哌甲酯会降低反应发散性,而在多巴胺合成能力较高的参与者中,哌甲酯会增强反应发散性。没有发现舒必利的任何作用的证据。这些结果表明,哌甲酯可以破坏某些形式的发散性创造力,但仅在基线多巴胺水平较低的个体中。