Galizio M., Robinson E.G., Ordronneau C.
Department of Psychology, University of North Carolina at Wilmington, Wilmington, NC 28403, USA.
Behav Pharmacol. 1994 Apr;5(2):125-130. doi: 10.1097/00008877-199404000-00003.
The effects of µ agonists fentanyl, methadone and morphine and kappa agonist U50,488 on behavior maintained by negative reinforcement were determined. Rats were trained on concurrent schedules in which pressing one lever postponed shock on a Sidman avoidance schedule and pressing the other lever produced signaled periods of timeout from avoidance on variable-ratio schedules. All of the µ agonists decreased responding maintained by timeout from avoidance at doses that increased or did not affect avoidance rates. The kappa agonist U50,488 decreased response rates in some rats, but increased responding in others. In no case was a selective reduction in responding on the timeout lever produced by U50,488. Thus, the previously reported selective decreases in timeout responding by morphine are also produced by µ agonists fentanyl and methadone, but not by kappa agonist U50, 488.
研究了μ阿片受体激动剂芬太尼、美沙酮和吗啡以及κ阿片受体激动剂U50,488对由负强化维持的行为的影响。对大鼠进行了并发程序训练,其中按压一个杠杆可在西德曼回避程序中推迟电击,按压另一个杠杆则在可变比率程序中产生有信号的回避超时时段。所有μ阿片受体激动剂在增加或不影响回避率的剂量下,都会降低由回避超时维持的反应。κ阿片受体激动剂U50,488在一些大鼠中降低了反应率,但在另一些大鼠中增加了反应。U50,488从未导致对超时杠杆的反应选择性降低。因此,先前报道的吗啡对超时反应的选择性降低,也可由μ阿片受体激动剂芬太尼和美沙酮产生,但κ阿片受体激动剂U50,488则不会。