Imaging gene-substance interactions: The effect of the DRD2 TaqIA polymorphism and the dopamine agonist bromocriptine on the brain activation during the anticipation of reward

被引:74
作者
Kirsch, Peter
Reuter, Martin
Mier, Daniela
Lonsdorf, Tina
Stark, Rudolf
Gallhofer, Bernd
Vaitl, Dieter
Hennig, Juergen
机构
[1] Univ Giessen, Ctr Psychiat, D-35385 Giessen, Germany
[2] Univ Giessen, Dept Psychol, D-35385 Giessen, Germany
[3] Univ Giessen, Bender Inst Neuroimaging, D-35385 Giessen, Germany
关键词
dopamine; DRD2; reward; addiction; fMRI; genetics;
D O I
10.1016/j.neulet.2006.07.030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dopamine is known as the main neurotransmitter modulating the activation of the reward system of the brain. The DRD2 TaqIA polymorphism is associated with dopamine D2 receptor density which plays an important role in the context of reward. Persons carrying an A1 allele have a lower D2 receptor density and a higher risk to show substance abuse. The present study was designed to investigate the influence of the DRD2 Taq1A polymorphism and the selective D2 receptor agonist bromociptine on the activation of the reward system by means of functional magnetic resonance imaging (fMRI). In a double-blind crossover study with 24 participants we found an increase of reward system activation from placebo to bromocriptine only in subjects carrying the A1 allele. Furthermore, only A1 carrier showed an increase of performance under bromocriptine. The results are interpreted as reflecting a specific sensitivity for dopamine agonists in persons carrying an A1 allele and may complement actual data and theories of the development of addiction disorders postulating a higher genetic risk for substance abuse in carrier of the A I allele. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:196 / 201
页数:6
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