Sansone M, Castellano C, Libri V
Istituto di Psicobiologia e Psicofarmacologia, CNR, Roma, Italy.
Psychopharmacology (Berl). 1988;95(2):176-9. doi: 10.1007/BF00174505.
The opioid agonist-antagonist pentazocine (1-30 mg/kg) and the partial agonist buprenorphine (0.05-0.25 mg/kg) were tested, alone or in combination with the histamine H1-receptor antagonist tripelennamine (1, 2.5, 5 or 10 mg/kg), on locomotor activity in mice of the CD-1 strain. When given alone, pentazocine produced slight and non-dose-related activity increments, while buprenorphine induced strong and dose-related locomotor stimulation. Tripelennamine slightly increased activity by itself and enhanced buprenorphine-, but not pentazocine-induced hyperactivity. The results are discussed in relation to the hypothesis that antihistaminic agents specifically interfere with locomotor effects of opioids.
对阿片类激动-拮抗剂喷他佐辛(1-30毫克/千克)和部分激动剂丁丙诺啡(0.05-0.25毫克/千克)进行了测试,它们单独使用或与组胺H1受体拮抗剂曲吡那敏(1、2.5、5或10毫克/千克)联合使用,以研究其对CD-1品系小鼠运动活性的影响。单独给药时,喷他佐辛产生轻微且与剂量无关的活性增加,而丁丙诺啡则诱导强烈且与剂量相关的运动刺激。曲吡那敏自身可轻微增加活性,并增强丁丙诺啡诱导的多动,但不增强喷他佐辛诱导的多动。本文根据抗组胺药特异性干扰阿片类药物运动效应这一假说对结果进行了讨论。