Ståhle L, Ungerstedt U
Eur J Pharmacol. 1984 Feb 17;98(2):307-10. doi: 10.1016/0014-2999(84)90608-3.
Yawning behaviour in rats was studied by direct observation. Apomorphine dose dependently induced yawning: 0.05 mg/kg was most effective, 0.2 mg/kg induced locomotor and sniffing behaviour but less yawning. Sulpinide (2 and 10 mg/kg) dose dependently blocked the apomorphine (0.05 mg/kg)-induced yawning. (+)-3-PPP (1-10 mg/kg) induced yawning in a manner similar to that of apomorphine but (-)-3-PPP (1-10 mg/kg) did so only weakly. Yawning induced by (+)-3-PPP was blocked by sulpiride 10 mg/kg. It is concluded that (+)-3-PPP but not (-)-3-PPP is at least as effective as apomorphine to induce yawning in rats, indicating that (+)-3-PPP, but not (-)-3-PPP, is a pure agonist on dopamine autoreceptors.
通过直接观察研究了大鼠的打哈欠行为。阿扑吗啡剂量依赖性地诱导打哈欠:0.05mg/kg最有效,0.2mg/kg诱导运动和嗅探行为,但打哈欠较少。舒必利(2和10mg/kg)剂量依赖性地阻断阿扑吗啡(0.05mg/kg)诱导的打哈欠。(+)-3-PPP(1-10mg/kg)以类似于阿扑吗啡的方式诱导打哈欠,但(-)-3-PPP(1-10mg/kg)诱导作用较弱。10mg/kg舒必利可阻断(+)-3-PPP诱导的打哈欠。结论是,(+)-3-PPP而非(-)-3-PPP在诱导大鼠打哈欠方面至少与阿扑吗啡一样有效,这表明(+)-3-PPP而非(-)-3-PPP是多巴胺自身受体上的纯激动剂。