Schindler C W, White M F, Goldberg S R
NIDA Addiction Research Center, Baltimore, MD 21224.
Psychopharmacology (Berl). 1990;101(2):172-7. doi: 10.1007/BF02244122.
Locomotor activity was studied in the rabbit following injections of morphine, ethylketocyclazocine and N-allylnormetazocine. All three drugs produced only depression of activity. The opioid antagonist naloxone antagonized the effects of both morphine and ethylketocyclazocine. Naloxone (0.1 mg/kg) did not antagonize the effects of N-allylnormetazocine. Naloxone alone depressed locomotor activity at doses above 0.3 mg/kg. This effect of naloxone was partially antagonized by 0.1 mg/kg ethylketocyclazocine, but not by 0.1 mg/kg morphine. The GABA agonist muscimol (0.1 and 1.0 mg/kg) also did not antagonize the effect of naloxone on locomotor activity. Finally, amphetamine did not produce a great deal of locomotor activation in the rabbit, which may indicate that increasing activity in the rabbit by drug intervention may be inherently difficult. These results indicate that the opioids have effects in the rabbit that are clearly different from those observed in rodents, where morphine and N-allylnormetazocine have been reported to produce locomotor activation, and naloxone typically has little effect. In addition, the effects of the opioids on locomotor activity were clearly distinguishable from their effects on learning in the rabbit. While morphine and ethylketocyclazocine were approximately equipotent in depressing locomotor activity, morphine is much less potent than ethylketocyclazocine in retarding acquisition of the classically conditioned nictitating membrane response in the rabbit.
研究了家兔注射吗啡、乙基酮环唑辛和N-烯丙基去甲左啡诺后的运动活动。这三种药物均只引起活动抑制。阿片类拮抗剂纳洛酮可拮抗吗啡和乙基酮环唑辛的作用。纳洛酮(0.1毫克/千克)不能拮抗N-烯丙基去甲左啡诺的作用。单独使用纳洛酮时,剂量高于0.3毫克/千克会抑制运动活动。纳洛酮的这种作用可被0.1毫克/千克的乙基酮环唑辛部分拮抗,但不能被0.1毫克/千克的吗啡拮抗。γ-氨基丁酸(GABA)激动剂蝇蕈醇(0.1和1.0毫克/千克)也不能拮抗纳洛酮对运动活动的作用。最后,苯丙胺在家兔中并未产生大量的运动激活,这可能表明通过药物干预增加家兔的活动可能本来就很困难。这些结果表明,阿片类药物在家兔中的作用明显不同于在啮齿动物中观察到的作用,在啮齿动物中,据报道吗啡和N-烯丙基去甲左啡诺会产生运动激活,而纳洛酮通常作用很小。此外,阿片类药物对运动活动的作用明显不同于它们对家兔学习的作用。虽然吗啡和乙基酮环唑辛在抑制运动活动方面大致等效,但在延缓家兔经典条件反射性瞬膜反应的获得方面,吗啡的效力远低于乙基酮环唑辛。