Negus S S, Picker M J, Dykstra L A
Curriculum in Neurobiology, University of North Carolina, Chapel Hill 27599.
Psychopharmacology (Berl). 1990;102(4):465-73. doi: 10.1007/BF02247126.
The present study was designed to explore the nature of the interaction between mu and kappa opioid agonists in the rat drug discrimination procedure. In rats trained to discriminate the kappa agonist U50,488 (5.6 mg/kg) from water, the other kappa agonist bremazocine substituted completely for the U50,488 training stimulus, and the additional kappa agonist tifluadom substituted in three of five of rats tested. In contrast, the mu agonists morphine, fentanyl, and buprenorphine produced primarily vehicle-appropriate responding. When morphine, fentanyl, and buprenorphine were combined with the training dose of U50,488, all three mu agonists reduced U50,488-appropriate responding. In rats trained to discriminate the mu agonist morphine (10.0 mg/kg) from saline, the other mu agonists morphine and buprenorphine all substituted in a dose-dependent manner for the morphine training stimulus, whereas U50,488, bremazocine, and tifluadom produced primarily vehicle-appropriate responding. When combined with the training dose of morphine, bremazocine antagonized morphine's discriminative stimulus effects, whereas U50,488 and tifluadom had no effect. The barbiturate pentobarbital neither substituted for, nor antagonized, the discriminative stimulus effects of either U50,488 or morphine. These results suggest that mu agonists and kappa agonists produce interacting effects in the drug discrimination procedure in rats.
本研究旨在探讨μ和κ阿片类激动剂在大鼠药物辨别程序中的相互作用性质。在经过训练以区分κ激动剂U50,488(5.6毫克/千克)和水的大鼠中,另一种κ激动剂布马佐辛完全替代了U50,488训练刺激,并且另一种κ激动剂替氟朵在五只受试大鼠中的三只中产生了替代作用。相比之下,μ激动剂吗啡、芬太尼和丁丙诺啡主要产生与溶剂相符的反应。当吗啡、芬太尼和丁丙诺啡与U50,488的训练剂量合用时,所有三种μ激动剂均降低了与U50,488相符的反应。在经过训练以区分μ激动剂吗啡(10.0毫克/千克)和生理盐水的大鼠中,其他μ激动剂吗啡和丁丙诺啡均以剂量依赖性方式替代了吗啡训练刺激,而U50,488、布马佐辛和替氟朵主要产生与溶剂相符的反应。当与吗啡的训练剂量合用时,布马佐辛拮抗吗啡的辨别刺激作用,而U50,488和替氟朵则无作用。巴比妥类药物戊巴比妥既不能替代也不能拮抗U50,488或吗啡的辨别刺激作用。这些结果表明,μ激动剂和κ激动剂在大鼠药物辨别程序中产生相互作用。