Sufka K J, Hughes R A
Department of Psychology, Iowa State University, Ames 50011-3180.
Pharmacol Biochem Behav. 1992 Feb;41(2):349-53. doi: 10.1016/0091-3057(92)90109-s.
Recent research demonstrated that codeine produced hypoalgesia and morphine produced hyperalgesia against a noxious thermal stimulus in young domestic fowl. The bidirectional effects of these opiate agonists on nociception are inconsistent with the notion that codeine's algesic effects result through in vivo demethylation of codeine to yield morphine. In Experiment 1, the temporal pattern (15,30,60 and 120 min) of codeine (30 mg/kg) effects on thermal nociception and respiration were examined in 15-day-old cockerels. Codeine produced a time-dependent biphasic response: hypoalgesia at 15 min and hyperalgesia at 60 and 120 min. Respiration was depressed by codeine at all test intervals. To assess for opioid specificity, Experiment 2 examined the action of naloxone (5 mg/kg) on the temporal pattern (15 and 60 min) of codeine effects (30 mg/kg) on thermal nociception and respiration. Bidirectional codeine algesic effects were observed at the 15- and 60-min test intervals. Naloxone increased the codeine jump latency scores at the 15-min interval and decreased codeine jump latency scores at the 60-min interval. These results suggest that codeine engages opposed nonopioid-mediated hypoalgesic and opioid-mediated hyperalgesic nociceptive systems in this animal model. Codeine depressed respiration at both the 15- and 60-min test intervals and this respiratory depression was reversed by naloxone. These findings support the notion that codeine respiratory effects are mediated by opioid system activity.
近期研究表明,在雏鸡中,可待因对有害热刺激产生痛觉减退作用,而吗啡则产生痛觉过敏作用。这些阿片类激动剂对伤害感受的双向作用与可待因的镇痛作用是通过其在体内脱甲基生成吗啡这一观点不一致。在实验1中,研究了15日龄公鸡中可待因(30毫克/千克)对热伤害感受和呼吸作用的时间模式(15、30、60和120分钟)。可待因产生了时间依赖性的双相反应:15分钟时痛觉减退,60和120分钟时痛觉过敏。在所有测试时间间隔内,可待因均使呼吸受到抑制。为评估阿片类特异性,实验2研究了纳洛酮(5毫克/千克)对可待因(30毫克/千克)作用于热伤害感受和呼吸的时间模式(15和60分钟)的影响。在15分钟和60分钟的测试时间间隔均观察到了可待因的双向镇痛作用。纳洛酮在15分钟时间间隔时增加了可待因跳跃潜伏期分数,在60分钟时间间隔时降低了可待因跳跃潜伏期分数。这些结果表明,在该动物模型中,可待因激活了相反的非阿片类介导的痛觉减退和阿片类介导的痛觉过敏伤害感受系统。可待因在15分钟和60分钟测试时间间隔均抑制了呼吸,且这种呼吸抑制被纳洛酮逆转。这些发现支持了可待因的呼吸作用是由阿片类系统活性介导的这一观点。