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抗抑郁药与右旋苯丙胺对可变间隔行为表现的相互作用。

Interaction between antidepressants and d-amphetamine on variable-interval performance.

作者信息

Shah K, Bradshaw C M, Szabadi E

机构信息

Department of Psychiatry, University of Manchester, UK.

出版信息

Psychopharmacology (Berl). 1990;100(4):548-54. doi: 10.1007/BF02244010.

Abstract

Four experiments were carried out investigating the interactions between some antidepressant drugs (imipramine, desipramine, fluvoxamine, trazodone (4 and 8 mg/kg) and d-amphetamine (0.1-3.2 mg/kg) on operant behaviour maintained under a variable-interval 80-s schedule of sucrose reinforcement; each experiment employed 12 rats. d-Amphetamine exerted a dose-related suppressant effect on response rate. Imipramine and desipramine given alone had no effect on response rate, whereas fluvoxamine (both doses) and the higher dose of trazodone produced significant increases in response rate. Pretreatment with imipramine, desipiramine or fluvoxamine significantly potentiated the suppressant effect of d-amphetamine on responding; pretreatment with trazodone had no significant effect. The potentiating effect of imipramine and desipramine may be related to their well known uptake blocking actions. The fact that fluvoxamine, a selective inhibitor of 5-hydroxytryptamine (5HT) uptake, also potentiated the effect of d-amphetamine suggests that the suppressant effect of d-amphetamine on operant behaviour may involve 5HT as well as catecholamine release. The lack of effect of trazodone may reflect its failure to influence uptake mechanisms. On the basis of a formal model couched in terms of Herrnstein's (1970) equation, it is suggested that imipramine, desipramine and fluvoxamine may have enhanced d-amphetamine's ability to reduce response capacity; it is suggested that the data do not provide evidence for an interaction between the antidepressants and the putative "motivation-enhancing" effect of d-amphetamine.

摘要

进行了四项实验,研究了一些抗抑郁药物(丙咪嗪、地昔帕明、氟伏沙明、曲唑酮(4和8毫克/千克))与右旋苯丙胺(0.1 - 3.2毫克/千克)之间对在可变间隔80秒蔗糖强化程序下维持的操作性行为的相互作用;每项实验使用12只大鼠。右旋苯丙胺对反应率产生剂量相关的抑制作用。单独给予丙咪嗪和地昔帕明对反应率没有影响,而氟伏沙明(两种剂量)和较高剂量的曲唑酮使反应率显著增加。用丙咪嗪、地昔帕明或氟伏沙明预处理显著增强了右旋苯丙胺对反应的抑制作用;用曲唑酮预处理没有显著影响。丙咪嗪和地昔帕明的增强作用可能与其众所周知的摄取阻断作用有关。5-羟色胺(5HT)摄取的选择性抑制剂氟伏沙明也增强了右旋苯丙胺的作用,这一事实表明,右旋苯丙胺对操作性行为的抑制作用可能涉及5HT以及儿茶酚胺的释放。曲唑酮缺乏作用可能反映了其未能影响摄取机制。基于以赫尔斯坦(1970)方程表述的形式模型,表明丙咪嗪、地昔帕明和氟伏沙明可能增强了右旋苯丙胺降低反应能力的能力;表明这些数据没有为抗抑郁药与右旋苯丙胺假定的“动机增强”作用之间的相互作用提供证据。

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