Suppr超能文献

曲马多与两种止吐药对小鼠伤害感受和胃肠转运的相互作用。

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

作者信息

Dürsteler Christian, Mases Anna, Fernandez Victor, Pol Olga, Puig Margarita M

机构信息

Department of Anaesthesiology, Hospital Universitario del Mar, Universidad Autónoma de Barcelona, Paseo Marítimo 25, 08003 Barcelona, Spain.

出版信息

Eur J Pain. 2006 Oct;10(7):629-38. doi: 10.1016/j.ejpain.2005.10.002. Epub 2005 Nov 21.

Abstract

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.

摘要

背景

临床研究表明,昂丹司琼可部分拮抗曲马多诱导的镇痛作用。

目的

研究曲马多与两种止吐药在小鼠抗伤害感受和胃肠转运方面的相互作用类型。

方法

我们评估了曲马多单独以及与昂丹司琼或氟哌利多联合使用时对雌性瑞士CD-1小鼠的抗伤害感受(乙酸扭体试验、足底试验)和抗转运(炭末)作用。采用等效线图和方差分析来确定相互作用类型。

结果

在扭体试验中,曲马多、昂丹司琼和氟哌利多各自均诱导了与剂量相关的伤害感受抑制。半数有效剂量(ED50)分别为:曲马多4.2±0.33mg/kg;昂丹司琼1.03±0.05mg/kg,氟哌利多1.00±0.14mg/kg。还获得了曲马多与昂丹司琼或氟哌利多按1:1固定比例联合使用时的剂量反应曲线。等效线图分析表明两种联合用药均存在拮抗作用。在足底试验中,曲马多的ED50为51.4±2.3mg/kg,但单独使用昂丹司琼或氟哌利多时无法获得剂量反应曲线。通过在固定剂量的昂丹司琼(0.1mg/kg)或氟哌利多(0.05mg/kg)存在的情况下对曲马多的剂量反应曲线来评估相互作用。结果显示曲马多 - 昂丹司琼之间存在拮抗作用(p<0.05),而曲马多 - 氟哌利多组合无相互作用。两种止吐药均拮抗了曲马多的抗转运作用。

结论

曲马多与昂丹司琼或氟哌利多在抗伤害感受方面的相互作用可能是拮抗或相加的,这取决于刺激类型。两种止吐药均拮抗曲马多的抗转运作用。结果表明曲马多与两种止吐药在镇痛和抑制胃肠转运方面存在拮抗作用,支持了先前的临床研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验