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通过泛化和交叉泛化实验证明的对麻醉药物提示特性敏感性的变化。

Changes of sensitivity to the cuing properties of narcotic drugs as evidenced by generalization and cross-generalization experiments.

作者信息

Colpaert F C, Niemegeers C J, Janssen P A

出版信息

Psychopharmacology (Berl). 1978 Jul 19;58(3):257-62. doi: 10.1007/BF00427388.

Abstract

With a discrete-trial, food-reward, two-lever procedure, rats were trained to discriminate 0.04 mg/kg fentanyl from saline. Individual threshold doses for generalization of fentanyl and for cross-generalization of morphine were determined repeatedly during a 17-week posttraining period. Threshold doses of both drugs almost continuously shifted in both the up- and downward direction. Shifts of fentanyl threshold doses covaried with those of morphine threshold doses. These shifts can best be described by a sustained oscillation, the mean amplitude of which amounts to a factor 3.65 of the dose-range for fentanyl, and to a factor 1.85 for morphine. The upper and lower limits of oscillation were symmetrical with respect to baseline. The oscillation can be described by a function expressing that the more distant a point along the function is from the baseline, the more it is susceptible to (positive/negative) acceleration along the intensity (i.e., dose) axis.

摘要

采用离散试验、食物奖励、双杠杆程序,训练大鼠区分0.04mg/kg芬太尼和生理盐水。在为期17周的训练后阶段,反复测定芬太尼泛化和吗啡交叉泛化的个体阈值剂量。两种药物的阈值剂量几乎持续上下波动。芬太尼阈值剂量的波动与吗啡阈值剂量的波动相关。这些波动最好用持续振荡来描述,其平均振幅相当于芬太尼剂量范围的3.65倍,吗啡的为1.85倍。振荡的上限和下限相对于基线是对称的。这种振荡可用一个函数来描述,该函数表示沿着函数离基线越远的点,就越容易在强度(即剂量)轴上产生(正/负)加速度。

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