David V, Durkin T P, Cazala P
Laboratoire de Neurosciences Comportementales et Cognitives, CNRS URA 339, Université de Bordeaux I, Talence, France.
Eur J Neurosci. 1998 Apr;10(4):1394-402. doi: 10.1046/j.1460-9568.1998.00150.x.
In order to study the functional role of the trans-synaptic neuronal interaction between glutamatergic afferents and mesolimbic dopaminergic neurons in internal reward processes, BALB/c male mice were unilaterally implanted with a guide-cannula, the tip of which was positioned 1.5 mm above the ventral tegmental area (VTA). On each day of the following experimental period, a stainless steel injection cannula was inserted into the VTA in order to study the eventual self-administration behaviour of either the competitive N-methyl-D-aspartate antagonist, D(-)-2-amino-7-phosphonoheptanoic acid (AP-7) or the alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid antagonist, 6,7-dinitroquinoxaline-2,3-dione (DNQX) (3 ng/50 nL) using a spatial discrimination task in a Y maze. Mice rapidly discriminated between the arm enabling a microinjection of either of these glutamatergic antagonists and the neutral arm of the maze, and a robust self-administration of either of these compounds was observed from the first session of acquisition. These data provide strong evidence that the intra-VTA microinjection of either of these subclasses of glutamatergic antagonist produces an effect which is interpreted centrally by the experimental subjects as being highly rewarding. Once the self-administration response had been fully acquired by the experimental subjects, preinjection of the dopaminergic D2 antagonist, sulpiride (50 mg/kg i.p.), 30 min before the test, produced a rapid extinction of the self-administration response. This latter result demonstrates the dopaminergic D2 receptor dependence of this intra-VTA self-administration of both of these subclasses of glutamatergic antagonist. We conclude that the different glutamatergic afferent neuronal inputs to the VTA globally exert, in vivo, via the mediation of interposed endogenous GABAergic interneurons, a tonic trans-synaptic inhibitory regulation of neuronal activity in the mesolimbic dopaminergic pathway and that this complex neuronal interaction in the VTA plays a significant functional part in the modulation of internal reward processes.
为了研究谷氨酸能传入神经与中脑边缘多巴胺能神经元之间的跨突触神经元相互作用在内在奖赏过程中的功能作用,将BALB/c雄性小鼠单侧植入引导套管,其尖端位于腹侧被盖区(VTA)上方1.5毫米处。在接下来的实验期间的每一天,插入一根不锈钢注射套管到VTA,以便使用Y迷宫中的空间辨别任务研究竞争性N-甲基-D-天冬氨酸拮抗剂D(-)-2-氨基-7-磷酸庚酸(AP-7)或α-氨基-3-羟基-5-甲基异恶唑-4-丙酸拮抗剂6,7-二硝基喹喔啉-2,3-二酮(DNQX)(3纳克/50纳升)最终的自我给药行为。小鼠能够迅速区分允许微量注射这些谷氨酸能拮抗剂之一的臂和迷宫的中性臂,并且从第一次习得训练开始就观察到对这些化合物中任何一种的强烈自我给药行为。这些数据提供了强有力的证据,表明在VTA内微量注射这些谷氨酸能拮抗剂的任何一个亚类都会产生一种效应,实验对象在中枢将其解释为极具奖赏性。一旦实验对象完全习得自我给药反应,在测试前30分钟腹腔注射多巴胺能D2拮抗剂舒必利(50毫克/千克)会使自我给药反应迅速消退。后一结果证明了VTA内这两个谷氨酸能拮抗剂亚类自我给药对多巴胺能D2受体的依赖性。我们得出结论,不同的谷氨酸能传入神经对VTA的神经元输入在体内通过中间内源性GABA能中间神经元的介导,对中脑边缘多巴胺能通路中的神经元活动进行紧张性跨突触抑制调节,并且VTA中这种复杂的神经元相互作用在内在奖赏过程的调节中发挥重要的功能作用。