Fidecka S
Department of Pharmacodynamics, Medical Academy, Lublin, Poland.
Pol J Pharmacol Pharm. 1987 Jan-Feb;39(1):33-40.
The effect of naloxone on the ketamine-induced anesthesia and analgesia, and the development of tolerance to ketamine and the cross-tolerance to morphine (measured by an analgesic effect) were investigated in the rat. Ketamine produced a dose-dependent analgesia. Naloxone, 1 mg/kg, significantly inhibited analgesia induced by ketamine, 100 mg/kg, but even in a dose of 4 mg/kg it did not affect the duration of anesthesia. A chronic administration of ketamine (100 mg/kg twice a day (b.i.d.) for 7 days) resulted in the development of tolerance to analgesic effects of ketamine. The analgesic action of morphine was attenuated in rats receiving ketamine chronically, while the analgesic effects of ketamine were significantly potentiated in morphine-dependent rats. Ketamine, 25 mg/kg, significantly attenuated the withdrawal signs evoked by naloxone in morphine-dependent rats. The results corroborate the suggestion about the participation of the central opioid neurotransmission in the mechanism of ketamine action.
在大鼠中研究了纳洛酮对氯胺酮诱导的麻醉和镇痛作用的影响,以及对氯胺酮耐受性的发展和对吗啡的交叉耐受性(通过镇痛作用测量)。氯胺酮产生剂量依赖性镇痛作用。1mg/kg的纳洛酮显著抑制100mg/kg氯胺酮诱导的镇痛作用,但即使剂量为4mg/kg,它也不影响麻醉持续时间。慢性给予氯胺酮(每天两次,每次100mg/kg,共7天)导致对氯胺酮镇痛作用产生耐受性。在长期接受氯胺酮的大鼠中,吗啡的镇痛作用减弱,而在吗啡依赖的大鼠中,氯胺酮的镇痛作用显著增强。25mg/kg的氯胺酮显著减轻了吗啡依赖大鼠中纳洛酮诱发的戒断症状。结果证实了关于中枢阿片类神经传递参与氯胺酮作用机制的推测。