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帕罗西汀是一种具有抗抑郁特性的选择性5-羟色胺摄取抑制剂,在啮齿动物的操作性药物辨别生物测定中缺乏苯丙胺样的刺激特性。

Paroxetine, a selective 5-hydroxytryptamine uptake inhibitor with antidepressant properties, lacks amphetamine-like stimulus properties in an operant drug discrimination bioassay in rodents.

作者信息

Goudie A J, Dubicki W, Leathley M

机构信息

Psychology Department, Liverpool University, UK.

出版信息

J Pharm Pharmacol. 1988 Mar;40(3):192-6. doi: 10.1111/j.2042-7158.1988.tb05217.x.

Abstract

To evaluate whether the novel antidepressant paroxetine has any possible amphetamine-like actions, rats were trained to discriminate (+)-amphetamine sulphate in a standard two lever operant drug discrimination (DD) procedure using a fixed ratio 10 schedule of food reinforcement with a quantal, lever selection, index of the amphetamine stimulus. The 'training' dose of amphetamine was 1 mg kg-1, i.p. Rats trained with this dose of amphetamine (n = 15) learned the drug discrimination rapidly over 30 training sessions and discriminative performance in these animals was subsequently maintained at a high level of accuracy (90% correct) over a prolonged time. In tests in these trained animals, amphetamine itself and the antidepressant agents nomifensine and tranylcypromine all produced clear, unequivocal dose-related generalization to amphetamine with ED50s of 0.2, 0.5 and 1.6 mg kg-1 respectively (as determined by probit analyses). In tests with paroxetine hydrochloride it was established that, over the dose range 0.3 to 10 mg kg-1, no evidence was seen of generalization to the amphetamine stimulus. These data confirm earlier studies which suggested that some antidepressants may possess abuse potential because of their ability to induce amphetamine-like internal states. In contrast, paroxetine is devoid of such properties.

摘要

为评估新型抗抑郁药帕罗西汀是否具有任何类似苯丙胺的作用,使用固定比率10的食物强化程序和苯丙胺刺激的定量杠杆选择指标,在标准的双杠杆操作性药物辨别(DD)程序中训练大鼠辨别硫酸(+)-苯丙胺。苯丙胺的“训练”剂量为1mg/kg,腹腔注射。用该剂量苯丙胺训练的大鼠(n = 15)在30次训练过程中迅速学会了药物辨别,并且这些动物的辨别性能随后在很长一段时间内保持在较高的准确度水平(90%正确)。在对这些经过训练的动物进行的测试中,苯丙胺本身以及抗抑郁药诺米芬辛和反苯环丙胺均产生了与苯丙胺明显、明确的剂量相关的泛化,其ED50分别为0.2、0.5和1.6mg/kg(通过概率分析确定)。在用盐酸帕罗西汀进行的测试中确定,在0.3至10mg/kg的剂量范围内,未发现对苯丙胺刺激有泛化的证据。这些数据证实了早期的研究,这些研究表明一些抗抑郁药可能因其诱导类似苯丙胺的内部状态的能力而具有滥用潜力。相比之下,帕罗西汀没有此类特性。

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