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在经过训练以检测可卡因辨别性刺激特性的大鼠中,食欲抑制药物的替代和交叉耐受情况。

Substitution and cross-tolerance profiles of anorectic drugs in rats trained to detect the discriminative stimulus properties of cocaine.

作者信息

Wood D M, Emmett-Oglesby M W

机构信息

Department of Pharmacology, Texas College of Osteopathic Medicine, Fort Worth 76107-2690.

出版信息

Psychopharmacology (Berl). 1988;95(3):364-8. doi: 10.1007/BF00181948.

Abstract

Rats were trained to discriminate cocaine, 10.0 mg/kg, using a two-lever operant procedure. Dose-effect data were determined for the substitution of cocaine, diethylpropion, methylphenidate, phenmetrazine, phentermine, and fenfluramine for the cocaine stimulus. All of these drugs, except fenfluramine, substituted fully for the cocaine stimulus. Subsequently, training was halted and cocaine, 20 mg/kg/8 h, was administered for 9 days, and dose-effect data were redetermined for all of these drugs on days 7-9 of chronic administration. Chronic administration of cocaine produced tolerance to the stimulus properties of cocaine, and cross-tolerance to the stimulus properties of methylphenidate, phenmetrazine, and phentermine, such that doses approximately two-fold higher than those used acutely were necessary to reproduce the original effect; the potency for the substitution of diethylpropion for the cocaine stimulus was decreased greater than four-fold; and fenfluramine still failed to substitute for the cocaine stimulus. These data suggest that 1) a common mechanism may mediate tolerance to the discriminative stimulus properties of cocaine, methylphenidate, phenmetrazine, and phentermine, and 2) tolerance in the drug discrimination procedure may have potential for establishing a comprehensive evaluation of dependence liability of CNS stimulants.

摘要

使用双杠杆操作性程序训练大鼠辨别10.0毫克/千克的可卡因。确定了可卡因、二乙丙胺苯丙酮、哌醋甲酯、苯甲吗啉、苯丁胺和芬氟拉明替代可卡因刺激的剂量效应数据。除芬氟拉明外,所有这些药物都能完全替代可卡因刺激。随后,停止训练并给予20毫克/千克/8小时的可卡因,持续9天,并在慢性给药的第7 - 9天重新确定所有这些药物的剂量效应数据。慢性给予可卡因会产生对可卡因刺激特性的耐受性,以及对哌醋甲酯、苯甲吗啉和苯丁胺刺激特性的交叉耐受性,以至于需要比急性使用时高约两倍的剂量才能重现原始效果;二乙丙胺苯丙酮替代可卡因刺激的效力降低超过四倍;并且芬氟拉明仍然不能替代可卡因刺激。这些数据表明:1)一种共同机制可能介导对可卡因、哌醋甲酯、苯甲吗啉和苯丁胺辨别刺激特性的耐受性,以及2)药物辨别程序中的耐受性可能有潜力用于建立对中枢神经系统兴奋剂依赖性的全面评估。

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