Department of Psychology, Vanderbilt University, Nashville, TN 37240, USA.
Science. 2010 Jul 30;329(5991):532. doi: 10.1126/science.1185778.
Dopamine (DA) has long been implicated in impulsivity, but the precise mechanisms linking human variability in DA signaling to differences in impulsive traits remain largely unknown. By using a dual-scan positron emission tomography approach in healthy human volunteers with amphetamine and the D2/D3 ligand [18F]fallypride, we found that higher levels of trait impulsivity were predicted by diminished midbrain D2/D3 autoreceptor binding and greater amphetamine-induced DA release in the striatum, which was in turn associated with stimulant craving. Path analysis confirmed that the impact of decreased midbrain D2/D3 autoreceptor availability on trait impulsivity is mediated in part through its effect on stimulated striatal DA release.
多巴胺(DA)长期以来一直与冲动有关,但将人类 DA 信号变化与冲动特质差异联系起来的精确机制在很大程度上仍然未知。通过在健康的人类志愿者中使用双重扫描正电子发射断层扫描方法,使用苯丙胺和 D2/D3 配体 [18F]氟拉必利,我们发现,较高的特质冲动性与纹状体中中脑 D2/D3 自身受体结合减少和更大的苯丙胺诱导的 DA 释放有关,这反过来又与兴奋剂渴望有关。路径分析证实,中脑 D2/D3 自身受体可用性减少对特质冲动性的影响部分是通过其对刺激纹状体 DA 释放的影响来介导的。