Ding Zheng-Ming, Liu Wen, Engleman Eric A, Rodd Zachary A, McBride William J
Indiana University School of Medicine, Institute of PsychiatricResearch, 791 Union Drive, Indianapolis, IN 46202-4887, USA.
Pharmacol Biochem Behav. 2009 May;92(3):404-12. doi: 10.1016/j.pbb.2009.01.004.
Previous findings indicated differences in neuronal circuitries mediating drug reinforcement between the anterior and posterior ventral tegmental area (VTA). The objective of the present study was to examine the effects of the dopamine D2 antagonist sulpiride and the GABA(A) antagonist picrotoxin administered in the anterior and posterior VTA on the activity of mesoaccumbal dopamine neurons in female Wistar rats. Sulpiride and picrotoxin were administered in the anterior and posterior VTA. Extracellular dopamine levels were measured in sub-regions of the VTA and nucleus accumbens (ACB). Reverse-microdialysis of sulpiride (100 microM) into the posterior VTA increased extracellular dopamine levels locally (80% above baseline) and in the ACB shell and core (70% above baseline), whereas reverse-microdialysis into the anterior VTA produced a much smaller effect locally (30% above baseline) and in the ACB shell and core. In contrast, microinjection of picrotoxin (80 and 160 microM) into the anterior, but not posterior VTA, increased dopamine release in the ACB shell. The results suggest that dopamine neurons in the posterior VTA, compared to the anterior VTA, may be under greater D2 receptor-mediated tonic inhibition, whereas dopamine neurons in the anterior VTA, compared to the posterior VTA, may be under greater GABA(A) receptor-mediated tonic inhibition.
先前的研究结果表明,腹侧被盖区(VTA)前部和后部之间介导药物强化作用的神经回路存在差异。本研究的目的是检测多巴胺D2拮抗剂舒必利和GABA(A)拮抗剂印防己毒素分别注入雌性Wistar大鼠VTA前部和后部后,对中脑伏隔核多巴胺能神经元活性的影响。将舒必利和印防己毒素分别注入VTA前部和后部。在VTA和伏隔核(ACB)的亚区域测量细胞外多巴胺水平。将舒必利(100微摩尔)反向微透析至VTA后部,可使局部细胞外多巴胺水平升高(比基线高80%),并使ACB壳核和核心区域的细胞外多巴胺水平升高(比基线高70%);而将舒必利反向微透析至VTA前部,局部和ACB壳核及核心区域产生的影响要小得多(比基线高30%)。相反,将印防己毒素(80和160微摩尔)注入VTA前部而非后部,可增加ACB壳核中的多巴胺释放。结果表明,与VTA前部相比,VTA后部的多巴胺能神经元可能受到更强的D2受体介导的紧张性抑制;而与VTA后部相比,VTA前部的多巴胺能神经元可能受到更强的GABA(A)受体介导的紧张性抑制。