Koshikawa N, Kitamura M, Kobayashi M, Cools A R
Department of Pharmacology, Nihon University, School of Dentistry, Tokyo, Japan.
Psychopharmacology (Berl). 1996 Aug;126(3):185-90. doi: 10.1007/BF02246447.
The goal of this study was to determine whether dopamine D2 and/or D1 receptors in the shell and the core of the nucleus accumbens of rats have a differential role in turning behaviour. Unilateral injection of a mixture of the dopamine D2 receptor agonist quinpirole (10 micrograms) and the dopamine D1 receptor agonist 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7, 8-diol (SKF 38393, 5 micrograms) into the shell of the nucleus accumbens produced contralateral turning, when doses which per se were ineffective were injected. This effect was far greater than that found after similar injections into the core of the nucleus accumbens. The effect elicited from the shell was significantly attenuated by prior administration of either the dopamine D2 receptor antagonist l-sulpiride (25 mg/0.5 microliters) or the dopamine D1 receptor antagonist (8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3-benzazepine-7-ol (SCH 23390, 0.5 micrograms/0.5 microliters) into the same region. These data together with the fact that l-sulpiride is known to be a valid tool to differentiate the involvement of distinct regions within the shell underlie the conclusion that dopamine D2 and D1 receptors in the shell, but not the core, of the nucleus accumbens play a critical role in the contralateral turning induced by unilateral injection of dopamine receptor agonists into this nucleus. The results are discussed in view of the known output pathways of the shell.
本研究的目的是确定大鼠伏隔核壳部和核心中的多巴胺D2和/或D1受体在旋转行为中是否具有不同作用。当注射本身无效的剂量时,向伏隔核壳部单侧注射多巴胺D2受体激动剂喹吡罗(10微克)和多巴胺D1受体激动剂1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓-7,8-二醇(SKF 38393,5微克)的混合物会产生对侧旋转。这种效应远大于向伏隔核核心进行类似注射后所发现的效应。预先向同一区域注射多巴胺D2受体拮抗剂L-舒必利(25毫克/0.5微升)或多巴胺D1受体拮抗剂(8-氯-2,3,4,5-四氢-3-甲基-5-苯基-1H-3-苯并氮杂卓-7-醇(SCH 23390,0.5微克/0.5微升)可显著减弱从壳部引发的效应。这些数据以及已知L-舒必利是区分壳部内不同区域参与情况的有效工具这一事实,共同支持了以下结论:伏隔核壳部而非核心中的多巴胺D2和D1受体在向该核单侧注射多巴胺受体激动剂所诱导的对侧旋转中起关键作用。结合壳部已知的输出通路对结果进行了讨论。