Fujimoto Atsushi, Elorette Catherine, Fujimoto Satoka H, Fleysher Lazar, Rudebeck Peter H, Russ Brian E
Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029
Lipschultz Center for Cognitive Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York 10029.
J Neurosci. 2025 Feb 5;45(6):e1301242024. doi: 10.1523/JNEUROSCI.1301-24.2024.
The neurotransmitter dopamine (DA) has a multifaceted role in healthy and disordered brains through its action on multiple subtypes of dopaminergic receptors. How the modulation of these receptors influences learning and motivation by altering intrinsic brain-wide networks remains unclear. Here, we performed parallel behavioral and resting-state functional MRI experiments after administration of two different DA receptor antagonists in male and female macaque monkeys. Systemic administration of SCH-23390 (D1 antagonist) slowed probabilistic learning when subjects had to learn new stimulus-reward associations and diminished functional connectivity (FC) in corticocortical and frontostriatal connections. In contrast, haloperidol (D2 antagonist) improved learning and broadly enhanced FC in cortical connections. Further comparisons between the effect of SCH-23390/haloperidol on behavioral and resting-state FC revealed specific cortical and subcortical networks associated with the cognitive and motivational effects of DA manipulation, respectively. Thus, we reveal distinct brain-wide networks that are associated with the dopaminergic control of learning and motivation via DA receptors.
神经递质多巴胺(DA)通过作用于多种多巴胺能受体亚型,在健康大脑和紊乱大脑中发挥多方面作用。这些受体的调节如何通过改变全脑固有网络来影响学习和动机仍不清楚。在此,我们在雄性和雌性猕猴中分别给予两种不同的多巴胺受体拮抗剂后,进行了并行的行为学和静息态功能磁共振成像实验。当受试者必须学习新的刺激 - 奖励关联时,系统性给予SCH - 23390(D1拮抗剂)会减缓概率学习,并减少皮质 - 皮质和额叶 - 纹状体连接中的功能连接(FC)。相比之下,氟哌啶醇(D2拮抗剂)则改善了学习,并广泛增强了皮质连接中的FC。对SCH - 23390/氟哌啶醇对行为和静息态FC的影响进行进一步比较后发现,分别有特定的皮质和皮质下网络与多巴胺操纵的认知和动机效应相关。因此,我们揭示了通过多巴胺受体与多巴胺对学习和动机的控制相关的不同全脑网络。