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氟哌啶醇对芬太尼-生理盐水辨别两种指标的差异效应。

Differential haloperidol effect on two indices of fentanyl-saline discrimination.

作者信息

Colpaert F C, Niemegeers C J, Janssen P A

出版信息

Psychopharmacology (Berl). 1977 Jul 18;53(2):169-73. doi: 10.1007/BF00426488.

Abstract

Using a discrete-trial, two-lever, food-reward discrimination learning paradigm, we trained rats (n = 6) to discriminate 0.04 mg/kg fentanyl (s.c. t-30') from saline. Stimulus generalization experiments with an adequate dose range (0.01-0.04 mg/kg) of fentanyl revealed that the ED50 value for drug lever selection is 0.02 mg/kg, irrespective of whether the animals were pretreated (s.c., t-60') with either saline or 0.08 mg/kg haloperidol. With increasing doses of the haloperidol-fentanyl combination, the percentage of total responding on the selected lever progressively decreased, and reached the 50% level at the highest drug combination. It is concluded that this percentage is heavily contaminated by factors unrelated to the discrimination condition being studied; these factors seem to invalidate this percentage as a discrimination index under experimental conditions (e.g., behaviorally toxic doses of drugs) where they are likely to operate. The use of response selection as a discrimination index in drug discrimination research is further argued.

摘要

采用离散试验、双杠杆、食物奖励辨别学习范式,我们训练了6只大鼠区分皮下注射30分钟后0.04mg/kg的芬太尼和生理盐水。对芬太尼适当剂量范围(0.01-0.04mg/kg)进行的刺激泛化实验表明,无论动物是预先皮下注射60分钟生理盐水还是0.08mg/kg氟哌啶醇,药物杠杆选择的半数有效剂量(ED50)值均为0.02mg/kg。随着氟哌啶醇-芬太尼组合剂量的增加,所选杠杆上的总反应百分比逐渐降低,在最高药物组合时达到50%的水平。得出的结论是,该百分比受到与所研究的辨别条件无关的因素的严重影响;在实验条件(如行为毒性剂量的药物)下,这些因素可能会使该百分比作为辨别指标失效。文中进一步论证了在药物辨别研究中使用反应选择作为辨别指标的问题。

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