Pinardi G, Sierralta F, Miranda H F
Pharmacology Program, ICBM, Faculty of Medicine, University of Chile, Santiago.
Inflammation. 2001 Aug;25(4):233-9. doi: 10.1023/a:1010923820109.
The interaction between the antinociceptive activity of ketoprofen and adrenergic agents was evaluated in the writhing test of mice. Dose-response curves were obtained for systemic and intrathecal antinociceptive effects of ketoprofen, phenylephrine, clonidine, desipramine, and prazosin; and ED50 were calculated. The interactions were evaluated by isobolographic analysis of the systemic or intrathecal co-administration of fixed-ratio combinations of ketoprofen with each adrenergic agent. The intraperitoneal combinations of ketoprofen with phenylephrine, clonidine, and prazosin showed supra-additivity, indicating that activation of alpha1 and alpha2 adrenoceptors play a role in nociceptive transmission at supraspinal levels. The same combinations given intrathecal were only additive. Desipramine intraperitoneal was also supra-additive: however, when ketoprofen was administered intrathecally with desipramine, only an additive interaction was obtained. The supra-additive interactions suggest that complementary mechanisms of antinociception have been activated, related with interference with the multiplicity of receptors and systems involved in the transmission of the nociceptive information. Racemic ketoprofen has an antinociceptive activity which is probably not only due to COX inhibition but also involves noradrenergic systems at spinal and supraspinal levels.
在小鼠扭体试验中评估了酮洛芬的抗伤害感受活性与肾上腺素能药物之间的相互作用。获得了酮洛芬、去氧肾上腺素、可乐定、地昔帕明和哌唑嗪全身及鞘内抗伤害感受作用的剂量-反应曲线,并计算了半数有效剂量(ED50)。通过对酮洛芬与每种肾上腺素能药物固定比例组合进行全身或鞘内联合给药的等效应线图分析来评估相互作用。酮洛芬与去氧肾上腺素、可乐定和哌唑嗪的腹腔内组合显示出超相加性,表明α1和α2肾上腺素能受体的激活在脊髓上水平的伤害性感受传递中起作用。鞘内给予相同组合仅具有相加性。腹腔内地昔帕明也具有超相加性:然而,当酮洛芬与地昔帕明鞘内联合给药时,仅获得相加性相互作用。超相加性相互作用表明已激活了抗伤害感受的互补机制,这与干扰伤害性信息传递中涉及的多种受体和系统有关。消旋酮洛芬具有抗伤害感受活性,这可能不仅归因于环氧化酶(COX)抑制,还涉及脊髓和脊髓上水平的去甲肾上腺素能系统。