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美普他酚的镇痛活性取决于阿片类和胆碱能机制。

The antinociceptive activity of meptazinol depends on both opiate and cholinergic mechanisms.

作者信息

Bill D J, Hartley J E, Stephens R J, Thompson A M

出版信息

Br J Pharmacol. 1983 May;79(1):191-9. doi: 10.1111/j.1476-5381.1983.tb10512.x.

Abstract

1 Antinociceptive responses to meptazinol, morphine and oxotremorine and the effects of pretreatment with naloxone or scopolamine on these responses in mice and rats, were examined. 2 Meptazinol evoked larger increases in nociceptive thresholds in the mouse than in the rat, whereas morphine induced large increases in both species. Oxotremorine was both a more potent and a more effective antinociceptive agent in the mouse than in the rat. 3 Antinociceptive responses to meptazinol were consistently inhibited in animals pretreated with naloxone, whereas scopolamine attenuated the effects of meptazinol in some, particularly the mouse tail immersion test, but not in all of the procedures used. 4 Naloxone inhibited all antinociceptive responses to morphine, and scopolamine inhibited all responses to oxotremorine. However, there was no significant interaction between naloxone and oxotremorine or between scopolamine and various opioid analgesic agents. 5 These results indicate that meptazinol, unlike established opioid drugs, may induce antinociception by a dual action on opiate and cholinergic mechanisms.

摘要
  1. 研究了美普他酚、吗啡和氧化震颤素对小鼠和大鼠的抗伤害感受反应,以及用纳洛酮或东莨菪碱预处理对这些反应的影响。2. 美普他酚引起小鼠伤害感受阈值的升高幅度大于大鼠,而吗啡在两种动物中均引起大幅度升高。氧化震颤素在小鼠中是比在大鼠中更有效且更具效力的抗伤害感受剂。3. 用纳洛酮预处理的动物对美普他酚的抗伤害感受反应持续受到抑制,而东莨菪碱在某些情况下,特别是小鼠尾浸试验中减弱了美普他酚的作用,但并非在所使用的所有程序中都如此。4. 纳洛酮抑制对吗啡的所有抗伤害感受反应,东莨菪碱抑制对氧化震颤素的所有反应。然而,纳洛酮与氧化震颤素之间或东莨菪碱与各种阿片类镇痛药之间没有显著的相互作用。5. 这些结果表明,与已确立的阿片类药物不同,美普他酚可能通过对阿片和胆碱能机制的双重作用诱导抗伤害感受。

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