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(+)-奥沙普替林在大鼠中的辨别性刺激特性

Discriminative stimulus properties of (+)-oxaprotiline in rats.

作者信息

Filip M, Chojnacka-Wójcik E, Przegaliński E

机构信息

Institute of Pharmacology, Polish Academy of Sciences, Kraków.

出版信息

Pol J Pharmacol. 1993 Mar-Apr;45(2):151-6.

PMID:8401767
Abstract

Using a drug discrimination procedure on a fixed ratio (FR) 10 schedule of reinforcement, rats were trained to distinguish between the stimulus properties of the selective inhibitor of noradrenaline uptake (+)-oxaprotiline ((+)-OXA) and saline. Fifty per cent of the rats that learned to reliably discriminate (+)-OXA from saline, reached high discrimination accuracy. In substitution testing, maprotiline (MAP) and desipramine (DMI) produced dose-related responding on the (+)-OXA lever. (-)-OXA failed to show substitution. The results of our findings demonstrate that (+)-OXA may be used as a discriminative cue in rats. The NA uptake inhibition seems to be involved in the effect of this drug.

摘要

在固定比率(FR)10强化程序下使用药物辨别程序,训练大鼠区分去甲肾上腺素摄取选择性抑制剂(+)-奥沙普明((+)-OXA)和生理盐水的刺激特性。学会可靠区分(+)-OXA和生理盐水的大鼠中有50%达到了高辨别准确率。在替代测试中,马普替林(MAP)和地昔帕明(DMI)在(+)-OXA杆上产生了剂量相关反应。(-)-OXA未显示替代作用。我们的研究结果表明,(+)-OXA可用作大鼠的辨别线索。去甲肾上腺素摄取抑制似乎与该药物的作用有关。

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