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喷他佐辛与曲吡那敏相互作用的表征:药物辨别及μ受体结合测定

Characterization of the interaction of pentazocine and tripelennamine: drug discrimination and mu-receptor binding assay.

作者信息

Shook J E, Kallman M J, Martin B R, Dewey W L

出版信息

Pharmacol Biochem Behav. 1984 Dec;21(6):877-81. doi: 10.1016/s0091-3057(84)80068-4.

Abstract

Abuse of the combination of pentazocine (P) and tripelennamine (T) reputedly produces an opiate-like euphoria not obtainable from either drug alone. To determine if this effect is related to interactions at the behavioral or receptor levels we tested this combination in rats trained to discriminate morphine from saline and in mu-receptor binding assays. Displacement of 3H-DHM was compared in morphine-naive, dependent and withdrawn states to determine the importance of prior morphine exposure. The morphine training cue (3 mg/kg) generalized to P but not to T. Combinations of T (0.3 and 1.0 mg/kg) with "no effect" doses of P (1 and 3 mg/kg) resulted in greater than additive increases in morphine-like responding. 3H-DHM was displaced by P but not T in naive, dependent and withdrawn states. Specific dose combinations of T (1 nM) with P (1 nM, 10 nM, 100 nM) resulted in enhanced displacement of 3H-DHM and was not related to prior morphine exposure. We conclude that the addition of T to P increases the mu-like subjective effects of P and this effect may be due to enhanced affinity of P for the mu-receptor.

摘要

据报道,喷他佐辛(P)和曲吡那敏(T)联用会产生一种单独使用任何一种药物都无法获得的类阿片欣快感。为了确定这种效应是否与行为或受体水平的相互作用有关,我们在经过训练能够区分吗啡和生理盐水的大鼠以及μ受体结合试验中对这种联用进行了测试。在未接触吗啡、吗啡依赖和戒断状态下比较3H-DHM的置换情况,以确定先前接触吗啡的重要性。吗啡训练提示剂量(3mg/kg)可泛化至P,但不能泛化至T。T(0.3和1.0mg/kg)与“无效应”剂量的P(1和3mg/kg)联用导致吗啡样反应的增加大于相加效应。在未接触吗啡、吗啡依赖和戒断状态下,3H-DHM可被P置换,但不能被T置换。T(1nM)与P(1nM、10nM、100nM)的特定剂量组合导致3H-DHM的置换增强,且与先前接触吗啡无关。我们得出结论,在P中添加T会增加P的类μ主观效应,这种效应可能是由于P对μ受体的亲和力增强所致。

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