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钙通道阻滞剂与行为敏化

Calcium channel blockers and behavioral sensitization.

作者信息

Karler R, Turkanis S A, Partlow L M, Calder L D

机构信息

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

出版信息

Life Sci. 1991;49(2):165-70. doi: 10.1016/0024-3205(91)90029-b.

Abstract

Behavioral sensitization to amphetamine-induced stereotypy was previously shown to consist of two separable phenomena, induction and expression, both of which involve the excitatory amino acids (EAA). In the present experiments, the calcium channel blockers (CCB), nifedipine, diltiazem and verapamil, were shown to block both phenomena; these results are similar to those reported earlier for DNQX, an antagonist of the non-N-methyl-D-aspartate receptors for the EAA. The CCB, like DNQX, affect only that percentage of the stereotypic response which results from the sensitization reaction, without affecting the quantitative portion of the response attributable to the acute effect of amphetamine. The results support previous conclusions that the sensitization response consists of two quantitative components, only one of which involves the EAA. The antagonism exhibited by the CCB suggests that behavioral sensitization involves Ca++ and L-type calcium channels.

摘要

先前的研究表明,对苯丙胺诱导的刻板行为的行为敏化由两种可分离的现象组成,即诱导和表达,这两种现象均涉及兴奋性氨基酸(EAA)。在本实验中,钙通道阻滞剂(CCB)硝苯地平、地尔硫䓬和维拉帕米被证明可阻断这两种现象;这些结果与先前报道的关于DNQX(一种EAA非N-甲基-D-天冬氨酸受体拮抗剂)的结果相似。与DNQX一样,CCB仅影响由敏化反应引起的刻板反应的百分比,而不影响归因于苯丙胺急性作用的反应的定量部分。这些结果支持了先前的结论,即敏化反应由两个定量成分组成,其中只有一个涉及EAA。CCB表现出的拮抗作用表明行为敏化涉及Ca++和L型钙通道。

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