Morgan M J, Franklin K B
Department of Psychology, McGill University, Montreal, Quebec, Canada.
Pharmacol Biochem Behav. 1991 Oct;40(2):317-22. doi: 10.1016/0091-3057(91)90560-o.
The role played by dopamine D1 and D2 receptors in formalin test analgesia was explored by challenging D-amphetamine- and morphine-induced analgesia with mixed and selective D1 and D2 antagonists, and by examining the relative analgesic activity of mixed and selective D1 and D2 agonists. The mixed D1/D2 dopamine antagonist cis-flupenthixol (0.5 mg/kg), the D2 antagonist pimozide (0.5 mg/kg), and the D1 antagonist SCH 23390 (0.1 mg/kg) attenuated both D-amphetamine and morphine analgesia. The mixed D1/D2 agonist apomorphine and the selective D2 agonist quinpirole produced dose-dependent analgesia while the selective D1 agonist SKF 38393 was without effect. These data suggest that D1 receptors play an "enabling" role in D2 receptor-mediated analgesia in the formalin test.
通过用混合和选择性D1及D2拮抗剂挑战右旋苯丙胺和吗啡诱导的镇痛作用,并通过检测混合和选择性D1及D2激动剂的相对镇痛活性,来探究多巴胺D1和D2受体在福尔马林试验镇痛中的作用。混合D1/D2多巴胺拮抗剂顺式氟哌噻吨(0.5毫克/千克)、D2拮抗剂匹莫齐特(0.5毫克/千克)和D1拮抗剂SCH 23390(0.1毫克/千克)均减弱了右旋苯丙胺和吗啡的镇痛作用。混合D1/D2激动剂阿扑吗啡和选择性D2激动剂喹吡罗产生剂量依赖性镇痛,而选择性D1激动剂SKF 38393则无作用。这些数据表明,在福尔马林试验中,D1受体在D2受体介导的镇痛中起“促成”作用。