Morelli M, Longoni R, Spina L, Di Chiara G
Psychopharmacology (Berl). 1986;89(2):259-60. doi: 10.1007/BF00310640.
The ability of apomorphine to induce yawning (YWG) in normal and reserpinized rats and its interaction with SCH 23390, a potent and specific D-1 receptor antagonist, was studied. Apomorphine was more potent in inducing YWG in reserpine-pretreated as compared to control rats. SCH 23390, in low doses (0.05 mg/kg SC), was able to significantly reduce the YWG evoked by apomorphine both in control and in reserpine-pretreated rats. The results indicate that D-1 receptors contribute to YWG elicited by apomorphine and contradict the idea that this effect is mediated by DA autoreceptors.
研究了阿扑吗啡在正常大鼠和利血平化大鼠中诱导打哈欠(YWG)的能力及其与强效特异性D-1受体拮抗剂SCH 23390的相互作用。与对照大鼠相比,阿扑吗啡在利血平预处理的大鼠中诱导YWG的效力更强。低剂量(0.05 mg/kg皮下注射)的SCH 23390能够显著减少阿扑吗啡在对照大鼠和利血平预处理大鼠中诱发的YWG。结果表明,D-1受体参与了阿扑吗啡诱发的YWG,这与该效应由多巴胺自身受体介导的观点相矛盾。