Laviolette S R, van der Kooy D
Neurobiology Research Group, Department of Anatomy & Cell Biology, 1 King's College Circle, University of Toronto, Toronto, Canada, M5S 1A8.
Eur J Neurosci. 2001 Mar;13(5):1009-15. doi: 10.1046/j.1460-9568.2001.01458.x.
In the midbrain ventral tegmental area (VTA), both dopaminergic and nondopaminergic neural substrates mediate various behavioural reward phenomena. VTA GABAergic neurons are anatomically positioned to influence the activity of both the mesolimbic dopamine system and nondopamine efferents from the VTA. In order to examine the possible functional role of VTA GABA(A) receptors in neural reward processes, we performed discrete, bilateral microinjections of the GABA(A) receptor agonist, muscimol, or the GABA(A) receptor antagonist, bicuculline, into the VTA. Using a fully counterbalanced, unbiased conditioned place-preference paradigm, we demonstrate that activation of VTA GABA(A) receptors, with the GABA(A) receptor agonist muscimol (5--50 ng/microL), or inhibition of VTA GABA(A) receptors, with the GABA(A) receptor antagonist bicuculline (5--50 ng/microL), both produce robust rewarding effects. Furthermore, these rewarding effects can be pharmacologically dissociated: blockade of dopamine receptors with a dopamine receptor antagonist, alpha-flupenthixol (0.8 mg/kg; i.p.), or concurrent activation of VTA GABA(B) receptors with a GABA(B) receptor agonist, baclofen (70 ng/microL), blocked the rewarding properties of the GABA(A) receptor agonist, but had no effect on the rewarding properties of the GABA(A) receptor antagonist. These results suggest that, within the VTA, a single GABA(A) receptor substrate controls bidirectional reward signalling between dopaminergic and nondopaminergic brain reward systems.
在中脑腹侧被盖区(VTA),多巴胺能和非多巴胺能神经基质均介导各种行为奖赏现象。VTAγ-氨基丁酸(GABA)能神经元在解剖学上的位置能够影响中脑边缘多巴胺系统和VTA的非多巴胺传出神经的活动。为了研究VTAγ-氨基丁酸A(GABA(A))受体在神经奖赏过程中可能的功能作用,我们向VTA进行了离散的双侧微量注射GABA(A)受体激动剂蝇蕈醇或GABA(A)受体拮抗剂荷包牡丹碱。使用完全平衡、无偏倚的条件性位置偏好范式,我们证明用GABA(A)受体激动剂蝇蕈醇(5 - 50纳克/微升)激活VTA GABA(A)受体,或用GABA(A)受体拮抗剂荷包牡丹碱(5 - 50纳克/微升)抑制VTA GABA(A)受体,均产生强烈的奖赏效应。此外,这些奖赏效应在药理学上可分离:用多巴胺受体拮抗剂α-氟哌噻吨(0.8毫克/千克;腹腔注射)阻断多巴胺受体,或用GABA(B)受体激动剂巴氯芬(70纳克/微升)同时激活VTA GABA(B)受体,可阻断GABA(A)受体激动剂的奖赏特性,但对GABA(A)受体拮抗剂的奖赏特性无影响。这些结果表明,在VTA内,单一的GABA(A)受体底物控制着多巴胺能和非多巴胺能脑奖赏系统之间的双向奖赏信号传递。