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Interaction between tramadol and two anti-emetics on nociception and gastrointestinal transit in mice.

机译:曲马多和两种止吐药对小鼠的伤害感受和胃肠道转运的相互作用。

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BACKGROUND: Clinical studies suggest that tramadol-induced analgesia is partially antagonized by ondansetron. AIMS: To investigate the type of interaction between tramadol and two anti-emetics on antinociception and gastrointestinal transit in mice. METHODS: We assessed the antinociceptive (acetic acid writhing test, plantar test) and antitransit (charcoal meal) effects of tramadol individually, and combined with ondansetron or droperidol in female Swiss CD-1 mice. Isobolograms and analysis of variance were used to determine the type of interaction. RESULTS: In the writhing test, tramadol, ondansetron and droperidol, each induced dose-related inhibition of nociception. The ED(50)'s were: tramadol 4.2+/-0.33 mg kg(-1); ondansetron 1.03+/-0.05 mg kg(-1), and droperidol 1.00+/-0.14 mg kg(-1). Dose-response curves were also obtained with tramadol combined with ondansetron or droperidol at 1:1 fixed ratios. The isobolographic analysis demonstrated antagonism for both combinations. In the plantar test, the ED(50) for tramadol was 51.4+/-2.3 mg kg(-1), but no dose-response curves could be obtained with ondansetron or droperidol individually. The interaction was assessed from dose-response curves to tramadol in the presence of a fixed dose of ondansetron (0.1 mg kg(-1)) or droperidol (0.05 mg kg(-1)). The results show antagonism between tramadol-ondansetron (p<0.05) and no interaction for the tramadol-droperidol combination. Both anti-emetics antagonized the antitransit effects of tramadol. CONCLUSIONS: The interaction of tramadol with ondansetron or droperidol on antinociception can be antagonistic or additive, depending on the type of stimuli. Both anti-emetics antagonize the anti-transit effects of tramadol. The results demonstrate antagonism between tramadol and the two anti-emetics for analgesia and inhibition of gastrointestinal transit, supporting previous clinical studies.
机译:背景:临床研究表明,曲马多所致的镇痛作用被恩丹西酮部分拮抗。目的:研究曲马多和两种止吐药之间在小鼠抗伤害感受和胃肠道转运中的相互作用类型。方法:我们分别评估了曲马多的抗伤害性(乙酸扭体试验,足底试验)和抗转运(木炭粉)作用,并与雌性瑞士CD-1小鼠中的恩丹西酮或氟哌啶联用。等效线图和方差分析被用来确定相互作用的类型。结果:在扭体试验中,曲马多,恩丹西酮和氟哌利多分别诱导剂量相关的伤害感受抑制作用。 ED(50)为:曲马多4.2 +/- 0.33 mg kg(-1);恩丹西酮1.03 +/- 0.05 mg kg(-1)和氟哌啶1.00 +/- 0.14 mg kg(-1)。曲马多与恩丹西酮或氟哌利多以1:1固定比例联合使用也可得到剂量反应曲线。等效线描记法分析显示了两种组合的拮抗作用。在足底试验中,曲马多的ED(50)为51.4 +/- 2.3 mg kg(-1),但单独使用恩丹西酮或氟哌朵无法获得剂量反应曲线。在固定剂量的恩丹西酮(0.1 mg kg(-1))或氟哌啶(0.05 mg kg(-1))存在下,从对曲马多的剂量反应曲线评估相互作用。结果显示,曲马多-恩丹西酮之间有拮抗作用(p <0.05),曲马多-氟哌利多组合没有相互作用。两种止吐药均能拮抗曲马多的抗转运作用。结论:曲马多与恩丹西酮或氟哌利多在抗伤害感受性上的相互作用可能是拮抗性或加性的,具体取决于刺激的类型。两种止吐药均能拮抗曲马多的反转运作用。结果表明曲马多与两种止吐药之间有拮抗作用,用于镇痛和抑制胃肠道运输,支持先前的临床研究。

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