Tupala Erkki, Hall Håkan, Mantere Tuija, Räsänen Pirkko, Särkioja Terttu, Tiihonen Jari
Department of Forensic Psychiatry, Niuvanniemi Hospital, University of Kuopio, Finland.
Neuroimage. 2003 May;19(1):145-55. doi: 10.1016/s1053-8119(03)00060-0.
The role of the dopamine system in brain reward mechanisms and development of substance abuse is well-established with nucleus accumbens as a key structure in mediating these effects. Several studies on alcoholism have indicated defects in dopaminergic neurotransmission and alterations in dopamine receptor densities. However, it has remained unclear if the substance abuse-related dopaminergic defect is specifically associated with a certain receptor subtype. The aim of this study was to compare putative alterations of dopamine D(1,) D(2), and D(3) receptors in nucleus accumbens, amygdala, and substantia nigra among alcoholics and controls. We studied the densities of dopamine D(1) and D(3) receptors in brains of 9 type 1 alcoholics, 8 type 2 alcoholics, and 10 healthy controls by using postmortem human whole hemisphere autoradiography. The mean densities of dopamine D(1) and D(3) receptors were at the same level in all study groups. Combining these with our previous results, our data suggest that among type 1 alcoholics dopamine transporters are lower in nucleus accumbens and dopamine D(2), but not D(1) or D(3) receptors in nucleus accumbens and amygdala. Further, the densities of all these dopamine-binding sites among type 2 alcoholics are at the level of healthy controls. The results suggest that lower dopamine receptor density is specific for D(2) receptor and for type 1 alcoholism, which supports Cloninger's neurogenetic model of two alcoholic subtypes, and indicates the importance of classifying these subgroups separately when issues related to dopaminergic activity are studied.
多巴胺系统在大脑奖赏机制及药物滥用发展中的作用已得到充分证实,伏隔核是介导这些作用的关键结构。多项关于酒精中毒的研究表明多巴胺能神经传递存在缺陷,且多巴胺受体密度发生改变。然而,与药物滥用相关的多巴胺能缺陷是否与特定受体亚型存在特异性关联仍不明确。本研究旨在比较酗酒者与对照组伏隔核、杏仁核及黑质中多巴胺D(1)、D(2)和D(3)受体的假定改变。我们通过死后人类全脑半球放射自显影术研究了9例1型酗酒者、8例2型酗酒者及10名健康对照者大脑中多巴胺D(1)和D(3)受体的密度。所有研究组中多巴胺D(1)和D(3)受体的平均密度处于同一水平。结合我们之前的研究结果,我们的数据表明,在1型酗酒者中,伏隔核中的多巴胺转运体较低,伏隔核和杏仁核中的多巴胺D(2)受体较低,但D(1)或D(3)受体并非如此。此外,2型酗酒者中所有这些多巴胺结合位点的密度与健康对照者处于同一水平。结果表明,多巴胺受体密度降低是D(2)受体和1型酒精中毒所特有的,这支持了克隆宁格关于两种酒精中毒亚型的神经遗传学模型,并表明在研究与多巴胺能活性相关的问题时,分别对这些亚组进行分类的重要性。