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可卡因行为敏化与兴奋性氨基酸

Cocaine behavioral sensitization and the excitatory amino acids.

作者信息

Karler R, Calder L D, Bedingfield J B

机构信息

Department of Pharmacology, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Psychopharmacology (Berl). 1994 Jul;115(3):305-10. doi: 10.1007/BF02245070.

Abstract

Studies were conducted to identify neuroeffector systems involved in behavioral sensitization to cocaine-induced stereotypy in mice, and to compare the results with those from our previous amphetamine studies. The effects of eight relatively selective neuroeffector agonists and antagonists were measured in mice in order to identify specific functional changes associated with the sensitization. In contrast to amphetamine, the only neuroeffector response altered by cocaine sensitization was a decrease in convulsive threshold to kainate. The persistence of the change in convulsive threshold correlated with the persistence of behavioral sensitization. The induction of sensitization was blocked by pretreatment with four different classes of drugs, represented by haloperidol, dizocilpine, diltiazem and DNQX. These results suggest that the mechanism of induction to cocaine is similar to that of amphetamine; both the glutamate and dopaminergic systems appear to be involved in induction. The expression of the sensitized cocaine response was blocked by haloperidol, CPP and diltiazem. These results differed from those obtained previously insofar as CPP did not affect the expression of sensitization to amphetamine. Furthermore, DNQX, in contrast to its antagonism of the expression of amphetamine sensitization, did not affect the expression of cocaine sensitization. The pharmacological data suggest that the mechanism of induction differs from that of expression, and that the mechanism of expression for cocaine sensitization differs from that for amphetamine.

摘要

开展了多项研究,以确定参与小鼠对可卡因诱导刻板行为产生行为敏化的神经效应系统,并将结果与我们之前对苯丙胺的研究结果进行比较。为了确定与敏化相关的特定功能变化,在小鼠中测量了八种相对选择性的神经效应激动剂和拮抗剂的作用。与苯丙胺不同,可卡因敏化改变的唯一神经效应反应是对海藻酸的惊厥阈值降低。惊厥阈值变化的持续时间与行为敏化的持续时间相关。用四种不同类别的药物(以氟哌啶醇、地佐环平、地尔硫卓和 DNQX 为代表)预处理可阻断敏化的诱导。这些结果表明,可卡因的诱导机制与苯丙胺相似;谷氨酸能和多巴胺能系统似乎都参与了诱导过程。氟哌啶醇、CPP 和地尔硫卓可阻断可卡因敏化反应的表达。这些结果与之前获得的结果不同,因为 CPP 不影响对苯丙胺敏化的表达。此外,与 DNQX 对苯丙胺敏化表达的拮抗作用相反,它不影响可卡因敏化的表达。药理学数据表明,诱导机制与表达机制不同,可卡因敏化的表达机制与苯丙胺的表达机制也不同。

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