Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, VU University Amsterdam, De Boelelaan 1085, 1081 HV Amsterdam, The Netherlands.
Cereb Cortex. 2010 May;20(5):1064-70. doi: 10.1093/cercor/bhp167. Epub 2009 Aug 18.
A neuropsychological hallmark of attention deficit/hyperactivity disorder (ADHD) is the reduced ability to tolerate delay of reinforcement, leading to impulsive choice. Genetic association studies have implicated several genes involved in dopaminergic neurotransmission in ADHD. In this study, we investigated whether differences in the expression level of these dopamine-related genes of rats predict the individual level of impulsive choice. Among all frontostriatal brain regions tested, only in the medial prefrontal cortex (mPFC), we observed significant positive correlations between impulsive choice and transcript levels of the dopamine receptor D(1), the dopamine receptor D(5) and calcyon. Local mPFC infusions of the D(1)/D(5) receptor antagonist SCH 23390 and agonist SKF 38393 resulted in increased impulsive choice, in agreement with the idea that endogenous receptor D(1)/D(5) stimulation in the mPFC promotes the choice of large delayed rewards. Together, these data indicate that this class of dopamine receptors in the mPFC plays a pivotal role in impulsive choice, and aberrancies thereof might contribute to ADHD symptomatology.
注意缺陷多动障碍(ADHD)的神经心理学标志是对强化延迟的容忍能力降低,导致冲动选择。遗传关联研究表明,多巴胺能神经传递涉及 ADHD 中的几个基因。在这项研究中,我们研究了这些多巴胺相关基因在大鼠中的表达水平差异是否可以预测个体冲动选择的水平。在所有测试的额-纹状体脑区中,只有在内侧前额叶皮层(mPFC)中,我们观察到冲动选择与多巴胺受体 D1、多巴胺受体 D5 和钙调蛋白的转录水平之间存在显著正相关。局部 mPFC 输注多巴胺 D1/D5 受体拮抗剂 SCH 23390 和激动剂 SKF 38393 导致冲动选择增加,这与内源性 mPFC 中受体 D1/D5 刺激促进大延迟奖励选择的观点一致。综上所述,这些数据表明,mPFC 中的这一类多巴胺受体在冲动选择中起关键作用,其异常可能导致 ADHD 症状。