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匹哌氮酯、右旋苯丙胺、可卡因、可卡因类似物、阿扑吗啡及其他药物与条件性强化作用的对比性相互作用。

Contrasting interactions of pipradrol, d-amphetamine, cocaine, cocaine analogues, apomorphine and other drugs with conditioned reinforcement.

作者信息

Robbins T W, Watson B A, Gaskin M, Ennis C

出版信息

Psychopharmacology (Berl). 1983;80(2):113-9. doi: 10.1007/BF00427952.

Abstract

The effects of various psychomotor stimulant drugs and drugs outside this class were examined on the efficacy of stimuli previously paired with reinforcement or reward (conditioned reinforcers, CR) in controlling responding. Pipradrol (5-45 mumol/kg), d-amphetamine (1.25-15.0 mumol/kg), and the cocaine analogues WIN 35,428 (0.1-30.0 mumol/kg) and in one of two determinations WIN 35,065-2 (0.1-29.0 mumol/kg) all generally increased responding on a lever providing CR, but did not change or decreased responding on a lever providing no CR (NCR). Cocaine (5-125 mumol/kg) and chlordiazepoxide (3.75-60.0 mumol/kg) had no significant effects. Morphine (3.2-32.0 mumol/kg) and alpha-flupenthixol (0.02-2.0 mumol/kg) generally reduced responding on both levers. Apomorphine (0.1-1.0 mumol/kg) generally increased responding on both levers. Neurochemical data showed that d-amphetamine was generally more potent than pipradrol in its effects on in vitro monoamine uptake and release.

摘要

研究了各种精神运动性兴奋药物以及该类以外的药物对先前与强化或奖励配对的刺激(条件性强化物,CR)控制反应的效果。匹哌氮酯(5 - 45微摩尔/千克)、右旋苯丙胺(1.25 - 15.0微摩尔/千克)、可卡因类似物WIN 35,428(0.1 - 30.0微摩尔/千克)以及在两次测定中的一次的WIN 35,065 - 2(0.1 - 29.0微摩尔/千克)通常都会增加在提供CR的杠杆上的反应,但不会改变或减少在不提供CR(NCR)的杠杆上的反应。可卡因(5 - 125微摩尔/千克)和氯氮卓(3.75 - 60.0微摩尔/千克)没有显著影响。吗啡(3.2 - 32.0微摩尔/千克)和α-氟哌噻吨(0.02 - 2.0微摩尔/千克)通常会减少在两个杠杆上的反应。阿扑吗啡(0.1 - 1.0微摩尔/千克)通常会增加在两个杠杆上的反应。神经化学数据表明,右旋苯丙胺在体外对单胺摄取和释放的影响通常比匹哌氮酯更有效。

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