Serra G, Collu M, Gessa G L
Eur J Pharmacol. 1986 Jan 21;120(2):187-92. doi: 10.1016/0014-2999(86)90539-x.
Yawning was induced in rats by the (+) enantiomer of 3PPP, while (-)-3PPP was inactive. Yawning was present 24, but not 1, 6 and 12 h after reserpine treatment. The (+)-3PPP-induced yawning was antagonized by haloperidol and sulpiride but not by domperidone. Reserpine-induced yawning was antagonized by sulpiride and by alpha-methyltyrosine suggesting that this behavior may be induced by endogenously released dopamine. Reserpine-pretreatment potentiated (+)-3PPP-induced yawning. The results argue against the view that yawning is the behavioural correlate of autoreceptor-mediated inhibition of DA transmission, and suggest that this behaviour is due to the stimulation of a special population of central postsynaptic DA receptors.
3PPP的(+)对映体可诱导大鼠打哈欠,而(-)-3PPP则无此作用。利血平处理后24小时出现打哈欠现象,但在1、6和12小时未出现。氟哌啶醇和舒必利可拮抗(+)-3PPP诱导的打哈欠,但多潘立酮无此作用。舒必利和α-甲基酪氨酸可拮抗利血平诱导的打哈欠,提示这种行为可能由内源性释放的多巴胺诱导。利血平预处理可增强(+)-3PPP诱导的打哈欠。这些结果与打哈欠是自受体介导的多巴胺传递抑制的行为相关这一观点相悖,并提示这种行为是由于刺激了特殊的中枢突触后多巴胺受体群体所致。