Martin-Iverson M T, Ortmann R, Fibiger H C
Brain Res. 1985 Apr 15;332(1):59-67. doi: 10.1016/0006-8993(85)90389-0.
The role of central catecholaminergic systems in place preference conditioning produced by methylphenidate and nomifensine was investigated. Several doses of either methylphenidate or nomifensine produced alterations in place preferences, while desipramine (10 mg/kg), a relatively selective noradrenergic uptake inhibitor, was ineffective, Haloperidol (0.15-0.5 mg/kg) did not attenuate place preferences induced with methylphenidate (2.5 and 5.0 mg/kg) or nomifensine (5.0 mg/kg), although conditioning with methylphenidate (5.0 mg/kg) was blocked after injections of a high dose of haloperidol (1.0 mg/kg). Intraventricular injections of 6-hydroxydopamine had no effect on methylphenidate (2.5 mg/kg) induced place preferences. In contrast, pretreatment with haloperidol (0.2 mg/kg) or intraventricular injections of 6-hydroxydopamine attenuated locomotor activity induced by methylphenidate (5.0 mg/kg). These results suggest that methylphenidate and nomifensine produce place preferences via mechanisms that are either qualitatively or quantitatively distinct from their catecholamine-dependent stimulant actions.
研究了中枢儿茶酚胺能系统在哌醋甲酯和诺米芬辛所致位置偏爱条件反射中的作用。几种剂量的哌醋甲酯或诺米芬辛均可引起位置偏爱的改变,而相对选择性的去甲肾上腺素摄取抑制剂地昔帕明(10毫克/千克)则无效。氟哌啶醇(0.15 - 0.5毫克/千克)不能减弱由哌醋甲酯(2.5和5.0毫克/千克)或诺米芬辛(5.0毫克/千克)诱导的位置偏爱,尽管在注射高剂量氟哌啶醇(1.0毫克/千克)后,由哌醋甲酯(5.0毫克/千克)引起的条件反射被阻断。脑室内注射6 - 羟基多巴胺对哌醋甲酯(2.5毫克/千克)诱导的位置偏爱没有影响。相反,氟哌啶醇(0.2毫克/千克)预处理或脑室内注射6 - 羟基多巴胺可减弱哌醋甲酯(5.0毫克/千克)诱导的运动活性。这些结果表明,哌醋甲酯和诺米芬辛产生位置偏爱的机制在性质或数量上与其依赖儿茶酚胺的兴奋作用不同。