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Subeffective doses of dexketoprofen trometamol enhance the potency and duration of fentanyl antinociception

机译:亚有效剂量的右酮洛芬曲美他莫可增强芬太尼抗伤害感受的效力和持续时间

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摘要

The combination of classic non-steroidal antiinflammatory drugs (NSAIDs) with opiates induces more analgesia than the summed effect of each drug given separately. No studies have been performed using new generation NSAIDs and fentanyl nor on the duration of this effect.We have studied the analgesic effect of fentanyl alone and after the administration of subeffective doses of dexketoprofen trometamol in rat nociceptive responses. The responses were evoked by noxious mechanical stimulation and were recorded as single motor units in male Wistar rats anaesthetized with α-chloralose.The effective dose 50 (ED50) observed with fentanyl was 22.4±1.5 μg kg−1 and full recovery was apparent 20 min later. The administration of a total dose of 40 μg kg−1 of dexketoprofen trometamol did not induce any significant effect on the nociceptive responses. In the presence of dexketoprofen trometamol, the ED50 for fentanyl was 5 fold lower than before: 3.8±1.1 μg kg−1 and no significant recovery was observed 45 min later. The opioid antagonist naloxone (200 μg kg−1) did not reverse the effect, although in control experiments the same dose was able to prevent any action of fentanyl given alone.We conclude that the combination of fentanyl and subeffective doses of dexketoprofen trometamol induces a more potent and longer lasting analgesic effect than that observed with fentanyl alone, and that this is not an opioid mediated action.
机译:经典的非甾体类抗炎药(NSAIDs)与鸦片类药物的组合比单独使用每种药物的总和能产生更多的镇痛作用。尚未使用新一代非甾体抗炎药和芬太尼对这种作用的持续时间进行任何研究。在有毒的机械刺激下引起反应,并以α-氯醛麻醉的雄性Wistar大鼠记录为单个运动单位。芬太尼观察到的有效剂量50(ED50)为22.4±1.5μgkg-1,完全恢复可见20 min。后来。给予总剂量为40μg/ kg-1的右酮洛芬特罗美他莫不会对伤害感受产生明显影响。在右旋酮洛芬的存在下,芬太尼的ED50比以前降低了5倍:3.8±1.1μg/ kg-1,45分钟后未见明显恢复。阿片拮抗剂纳洛酮(200μg/ kg-1)不能逆转这种作用,尽管在对照实验中,相同剂量的芬太尼可以单独预防芬太尼的任何作用。我们得出的结论是,芬太尼和亚有效剂量的右酮洛芬特罗美他酚联合使用可诱导比单独使用芬太尼观察到的镇痛作用更有效,更持久,这不是阿片类药物介导的作用。

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