Suppr超能文献

环氧化酶抑制剂与曲马多在醋酸诱导的小鼠扭体反应中相互作用的等效线图分析

Isobolographic analysis of interaction between cyclooxygenase inhibitors and tramadol in acetic acid-induced writhing in mice.

作者信息

Satyanarayana Padi S V, Jain Naveen K, Singh Amarjit, Kulkarni Shrinivas K

机构信息

Pharmacology Division, University Institute of Pharmaceutical Sciences, Panjab University, Chandigarh-160014, India.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2004 Jul;28(4):641-9. doi: 10.1016/j.pnpbp.2004.01.015.

Abstract

Non-steroidal anti-inflammatory drugs (NSAIDs) and opioids are the most commonly used analgesics in the management of acute and chronic pain. Combined use of NSAIDs and opioids has been indicated for achieving better analgesia with reduced side effects. The present study was aimed at evaluating the combination of different NSAIDs, which inhibit cyclooxygenase (COX) enzymes and tramadol against acetic acid-induced writhing in mice. The expected beneficial effect of combination regimen was analyzed by isobolographic analysis. The oral and intrathecally administered tramadol, a mu-opioid and naproxen, a nonselective COX inhibitor produced dose-dependent antinociception, however, rofecoxib, a selective COX-2 inhibitor lacked analgesic efficacy in writhing test. Isobolographic analysis showed synergistic or supra-additive interactions for the combinations of naproxen and tramadol after oral and intrathecal administration. However, similar interaction was not observed when tramadol was combined with rofecoxib. Pretreatment with naloxone partially reversed the antinociceptive effect of tramadol per se and its combination with naproxen without modifying the per se effect of NSAID. The results demonstrated marked synergistic interaction between naproxen and tramadol and such interaction involved opioid as well as non-opioid mechanisms of tramadol and inhibition of COX-1 but not COX-2 by naproxen.

摘要

非甾体抗炎药(NSAIDs)和阿片类药物是治疗急慢性疼痛最常用的镇痛药。NSAIDs与阿片类药物联合使用已被证明可在减少副作用的情况下实现更好的镇痛效果。本研究旨在评估不同的抑制环氧化酶(COX)的NSAIDs与曲马多联合使用对醋酸诱导的小鼠扭体反应的影响。通过等高线图分析来分析联合用药方案的预期有益效果。口服和鞘内注射曲马多(一种μ阿片类药物)和萘普生(一种非选择性COX抑制剂)可产生剂量依赖性的抗伤害感受作用,然而,选择性COX-2抑制剂罗非昔布在扭体试验中缺乏镇痛效果。等高线图分析显示,口服和鞘内注射后,萘普生与曲马多联合使用具有协同或超相加相互作用。然而,曲马多与罗非昔布联合使用时未观察到类似的相互作用。用纳洛酮预处理可部分逆转曲马多本身及其与萘普生联合使用时的抗伤害感受作用,而不改变NSAIDs本身的作用。结果表明萘普生与曲马多之间存在明显的协同相互作用,这种相互作用涉及曲马多的阿片类和非阿片类机制,以及萘普生对COX-1而非COX-2的抑制作用。

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