Suppr超能文献

纳布啡可降低曲马多诱导的小鼠奖赏效应,同时增强其镇痛作用。

Nalbuphine could decrease the rewarding effect induced by tramadol in mice while enhancing its antinociceptive activity.

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Zagazig University, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Zagazig University, Egypt; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tabuk University, Saudi Arabia.

出版信息

Eur J Pharmacol. 2015 Jul 5;758:11-5. doi: 10.1016/j.ejphar.2015.03.062. Epub 2015 Apr 3.

Abstract

Nalbuphine, a kappa-opioid agonist and mu-opioid partial agonist, has been used as an analgesic or an adjuvant with morphine to attenuate the development of morphine dependence and rewarding effect. In this study, we investigated the effect of nalbuphine on tramadol rewarding effect and antinociception. Using the conditioned place preference (CPP) paradigm in mice, we demonstrated that co-administration of nalbuphine (7mg/kg, s.c.) with tramadol (70mg/kg, s.c.) during conditioning completely blocked the CPP induced by tramadol. Co-administration of nalbuphine blocked the increase in dopamine level in the nucleus accumbens induced by tramadol. These actions were accompanied by an increase rather than attenuation of the antinociceptive effect of tramadol. These results suggest that nalbuphine could have a great potential as a pharmacotherapy for tramadol abuse.

摘要

纳布啡是一种κ阿片受体激动剂和μ阿片受体部分激动剂,已被用作镇痛剂或与吗啡合用的辅助药物,以减轻吗啡依赖和奖赏效应的发展。在这项研究中,我们研究了纳布啡对曲马多奖赏效应和镇痛作用的影响。使用小鼠条件性位置偏爱(CPP)范式,我们证明,在条件作用期间,纳布啡(7mg/kg,sc)与曲马多(70mg/kg,sc)共同给药完全阻断了曲马多引起的 CPP。纳布啡共同给药阻断了曲马多诱导的伏隔核多巴胺水平的增加。这些作用伴随着曲马多镇痛作用的增强而不是减弱。这些结果表明,纳布啡可能是治疗曲马多滥用的一种有前途的药物治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验