Meyer M E
Department of Psychology, University of Florida, Gainesville 32611.
Pharmacol Biochem Behav. 1993 Aug;45(4):843-7. doi: 10.1016/0091-3057(93)90130-l.
The present study examined the effects of the dopamine D1 and D5 subtype receptors agonist, R(+)-1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepine-7,8-diol (SK&F38393), and antagonist, R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-ben zaz epine (SCH23390), on locomotor activities after bilateral microinjection into the nucleus accumbens (Acb). SK&F38393 (0.1-10.0 micrograms) significantly potentiated and SCH23390 (0.01-1.0 microgram) significantly attenuated locomotor activity as measured by horizontal distance in cm. The data were supportive of the hypothesis that dose-related locomotor activities induced by microinjections of SK&F38393 into the Acb are independently mediated by D1 and D5 subtype receptors.
本研究检测了多巴胺D1和D5亚型受体激动剂R(+)-1-苯基-2,3,4,5-四氢-(1H)-3-苯并氮杂卓-7,8-二醇(SK&F38393)以及拮抗剂R(+)-7-氯-8-羟基-3-甲基-1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓(SCH23390)双侧微量注射入伏隔核(Acb)后对运动活动的影响。通过以厘米为单位的水平距离测量,SK&F38393(0.1 - 10.0微克)显著增强了运动活动,而SCH23390(0.01 - 1.0微克)显著减弱了运动活动。这些数据支持以下假设:向伏隔核微量注射SK&F38393所诱导的与剂量相关的运动活动是由D1和D5亚型受体独立介导的。