Morin R A, Lyness W H
Pharmacol Biochem Behav. 1983 Jun;18(6):885-9. doi: 10.1016/s0091-3057(83)80010-0.
Pretreatment with uricosuric agents probenecid or sulfinpyrazone potentiate the analgesic effects of morphine sulfate as ascertained using the phenylquinone (PQ)-induced writhing test. Doses of either uricosuric agent at 50 mg/kg had no effect on the number of PQ-induced writhes in test animals while potentiating the analgesic effects of morphine. High doses of probenecid or sulfinpyrazone alone did produce decreases in PQ-induced writing. Probenecid (50 mg/kg) did not alter hot water tail flick latency nor did it influence morphine analgesia. Attempts to uncover the underlying mechanisms in the uricosuric agent plus morphine attenuation of PQ-induced writhing were directed towards a possible displacement of morphine from plasma binding sites. However, administration of N-methyl-H3-morphine and estimation of plasma and brain morphine concentrations indicate no differences in the uricosuric drug pretreated groups compared to controls. The conflicting results in the PQ writhing test vs. hot water tail flick might indicate a false positive response in the former test. On the other hand this might be indicative of differing analgesic mechanisms for different types of pain. If the latter is true, this drug interaction may prove clinically useful.
使用苯醌(PQ)诱发扭体试验确定,用促尿酸排泄剂丙磺舒或磺吡酮进行预处理可增强硫酸吗啡的镇痛效果。丙磺舒或磺吡酮剂量为50mg/kg时,对试验动物PQ诱发的扭体次数没有影响,但可增强吗啡的镇痛作用。单独使用高剂量的丙磺舒或磺吡酮确实会减少PQ诱发的扭体反应。丙磺舒(50mg/kg)既不改变热水甩尾潜伏期,也不影响吗啡镇痛效果。为揭示促尿酸排泄剂加吗啡减轻PQ诱发扭体反应的潜在机制,研究方向是探究其是否可能使吗啡从血浆结合位点上被置换出来。然而,给予N-甲基-H3-吗啡并测定血浆和脑内吗啡浓度后发现,与对照组相比,促尿酸排泄剂预处理组并无差异。PQ扭体试验与热水甩尾试验结果相互矛盾,这可能表明前一试验存在假阳性反应。另一方面,这可能表明不同类型疼痛的镇痛机制不同。如果后者属实,这种药物相互作用可能具有临床应用价值。