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三杆操作下咪达唑仑的药物辨别分析:I. 泛化和拮抗作用中的剂量依赖性差异

Drug discrimination analysis of midazolam under a three-lever procedure: I. Dose-dependent differences in generalization and antagonism.

作者信息

Sannerud C A, Ator N A

机构信息

Preclinical Pharmacology Laboratory, Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

J Pharmacol Exp Ther. 1995 Jan;272(1):100-11.

PMID:7815322
Abstract

Twelve rats were trained to discriminate two doses of midazolam, 0.32 and 3.2 mg/kg, from no drug under a three-lever, multiple-trials procedure (15-min time-out, 5-min fixed-ratio-10 schedule of food reinforcement). In tests, midazolam (0.0032-10 mg/kg), administered cumulatively within a session or acutely across sessions, produced dose-dependent increases in responding on the low-dose lever after 0.1 to 1.0 mg/kg and on the high-dose lever at higher doses in all rats. Flumazenil dose-dependently antagonized the discriminative stimulus effect of 3.2 mg/kg of midazolam in all rats but antagonism of the lower midazolam training dose was not obtained in all rats. Pentobarbital dose-dependently produced responding on the levers associated with the no-drug and 0.32-mg/kg midazolam conditions but not on the lever associated with 3.2 mg/kg of midazolam. These results differed from those that would have been predicted from studies in midazolam-trained rats in two-lever procedures. The muscle relaxant methocarbamol and nonsedative/anxiolytic drugs (morphine, caffeine and d-amphetamine) did not produce responding on the lever associated with either the low or high midazolam training dose. However, cocaine produced partial responding on the lever associated with the low midazolam dose. Thus, the discriminative stimulus effects of 3.2 mg/kg of midazolam were benzodiazepine-like and not a function of general sedative or muscle-relaxant effects. The 0.32-mg/kg midazolam training dose, in this context, appeared less specific than 3.2 mg/kg of midazolam. Taken together, the results suggest that not all differences among the training stimuli in this three-lever context reflect simple differences in dose.

摘要

采用三杆多重试验程序(15分钟超时,5分钟固定比率10食物强化程序),训练12只大鼠区分两种剂量的咪达唑仑(0.32和3.2毫克/千克)与无药物状态。在测试中,在一次实验内累积给予或跨实验急性给予咪达唑仑(0.0032 - 10毫克/千克),所有大鼠在0.1至1.0毫克/千克后,低剂量杆上的反应呈剂量依赖性增加,在更高剂量时高剂量杆上的反应呈剂量依赖性增加。氟马西尼在所有大鼠中剂量依赖性地拮抗3.2毫克/千克咪达唑仑的辨别刺激效应,但并非所有大鼠都能拮抗较低的咪达唑仑训练剂量。戊巴比妥在与无药物和0.32毫克/千克咪达唑仑条件相关的杆上剂量依赖性地产生反应,但在与3.2毫克/千克咪达唑仑相关的杆上不产生反应。这些结果与在双杆程序中对咪达唑仑训练大鼠的研究所预测的结果不同。肌肉松弛剂美索巴莫和非镇静/抗焦虑药物(吗啡、咖啡因和右旋苯丙胺)在与低或高咪达唑仑训练剂量相关的杆上均未产生反应。然而,可卡因在与低咪达唑仑剂量相关的杆上产生部分反应。因此,3.2毫克/千克咪达唑仑的辨别刺激效应类似苯二氮䓬类,并非一般镇静或肌肉松弛效应的作用。在此背景下,0.32毫克/千克咪达唑仑训练剂量似乎不如3.2毫克/千克咪达唑仑特异。综合来看,结果表明在这种三杆情境中,训练刺激之间的并非所有差异都反映剂量的简单差异。

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