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苯丙醇胺光学异构体对(+)苯丙胺训练大鼠的刺激作用。

Stimulus effects of phenylpropanolamine optical isomers in (+)amphetamine-trained rats.

作者信息

Young R, Glennon R A

机构信息

Department of Medicinal Chemistry, School of Pharmacy, Box 980540, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

Pharmacol Biochem Behav. 2000 Jul;66(3):489-94. doi: 10.1016/s0091-3057(00)00173-8.

Abstract

There are eight phenylpropanolamine optical isomers related in structure to the central stimulants methamphetamine and amphetamine. Some of these are quite well known, such as (-)ephedrine, whereas others are relatively obscure, such as (-)cathine. Although certain of these phenylpropanolamines, such as (-)ephedrine and (+)cathine, retain central stimulant activity and are about 10- to 25-fold less potent than (+)amphetamine, the eight phenylpropanolamines have been compared only once before in drug discrimination studies. This latter study employed (-)ephedrine as the training drug. Because there are striking similarities between (-)ephedrine and (+)amphetamine as training drugs, it was of interest to determine and compare the effect of all eight phenylpropanolamines in (+)amphetamine trained animals. Using rats trained to discriminate 1 mg/kg of (+)amphetamine from saline vehicle under a variable interval 15-s (VI 15-s) schedule of reinforcement, the (+)amphetamine stimulus generalized only to (-)ephedrine (ED(50) = 4. 5 mg/kg) and (+)cathine (ED(50) = 8.0 mg/kg), and both agents were at least 10 times less potent that (+)amphetamine (ED(50) = 0.37 mg/kg). These results stand in contrast to those obtained with the (-)ephedrine-trained animals where the ephedrine stimulus generalized to all of the phenylpropanolamines except for (-)pseudoephedrine and (-)cathine. It is concluded that although there might be some similarity between the (-)ephedrine and (+)amphetamine stimuli, there are clear differences between them as determined in tests of stimulus generalization under the conditions employed.

摘要

有八种苯丙醇胺光学异构体,其结构与中枢兴奋剂甲基苯丙胺和苯丙胺相关。其中一些相当知名,如(-)麻黄碱,而其他一些则相对不太为人所知,如(-)去甲伪麻黄碱。尽管这些苯丙醇胺中的某些,如(-)麻黄碱和(+)去甲伪麻黄碱,保留了中枢兴奋活性,且效力比(+)苯丙胺低约10至25倍,但这八种苯丙醇胺此前仅在药物辨别研究中被比较过一次。后一项研究使用(-)麻黄碱作为训练药物。由于(-)麻黄碱和(+)苯丙胺作为训练药物有显著相似性,因此确定并比较所有八种苯丙醇胺对(+)苯丙胺训练动物的影响很有意义。使用在可变间隔15秒(VI 15 - s)强化程序下训练以区分1毫克/千克(+)苯丙胺和生理盐水载体的大鼠,(+)苯丙胺刺激仅泛化至(-)麻黄碱(ED50 = 4.5毫克/千克)和(+)去甲伪麻黄碱(ED50 = 8.0毫克/千克),且这两种药物的效力均比(+)苯丙胺(ED50 = 0.37毫克/千克)至少低10倍。这些结果与用(-)麻黄碱训练的动物所获得的结果形成对比,在后者中,麻黄碱刺激泛化至除(-)伪麻黄碱和(-)去甲伪麻黄碱之外的所有苯丙醇胺。结论是,尽管(-)麻黄碱和(+)苯丙胺刺激之间可能存在一些相似性,但在所采用条件下的刺激泛化测试中确定,它们之间存在明显差异。

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