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血清素能调节对与重复使用苯丙胺治疗相关的行为敏化和去抑制作用的影响。

Effects of serotonergic manipulations on the behavioral sensitization and disinhibition associated with repeated amphetamine treatment.

作者信息

Olausson P, Engel J A, Söderpalm B

机构信息

Department of Pharmacology, Institute of Physiology and Pharmacology, Göteborg University, Box 431, SE-405 30, Göteborg, Sweden.

出版信息

Pharmacol Biochem Behav. 2000 May;66(1):211-20. doi: 10.1016/s0091-3057(00)00228-8.

DOI:10.1016/s0091-3057(00)00228-8
PMID:10837863
Abstract

This study investigated the effects of repeated amphetamine treatment on locomotor activity and behavioral inhibition in the elevated plus-maze, and the influence of serotonin (5-HT) neurotransmission on these behaviors. Acute administration of amphetamine (1.0 mg/kg subcutaneously [SC]) stimulated locomotor activity, which was attenuated by acute citalopram (5.0 mg/kg SC) pretreatment. Repeated daily treatment with amphetamine (15 days) sensitized the rats to the amphetamine-induced locomotor stimulation. Acute pretreatment with the 5-HT precursor l-5-hydroxytryptophan (5-HTP; 25 mg/kg IP) or chronic treatment with the selective 5-HT reuptake inhibitor citalopram (5.0 mg/kg SC, twice daily), did not alter the expression of amphetamine-induced locomotor sensitization. In the elevated plus-maze, animals subjected to repeated amphetamine treatment expressed behavioral disinhibition after amphetamine exposure (1.0 mg/kg SC; -35 min), which was antagonized both by acute 5-HTP and chronic citalopram treatment. In summary, these findings suggest that behavioral sensitization to amphetamine is associated with amphetamine-induced behavioral disinhibition, and that acute 5-HTP as well as chronic citalopram treatment counteract the expression of amphetamine-induced behavioral disinhibition, but not locomotor sensitization. It appears likely that the antagonistic effects of 5-HTP and citalopram on behavioral disinhibition derive from a drug-induced facilitation of brain 5-HT neurotransmission.

摘要

本研究调查了重复给予苯丙胺对高架十字迷宫中运动活动和行为抑制的影响,以及血清素(5-羟色胺,5-HT)神经传递对这些行为的影响。急性给予苯丙胺(皮下注射1.0毫克/千克)可刺激运动活动,而急性西酞普兰(皮下注射5.0毫克/千克)预处理可减弱这种刺激。每天重复给予苯丙胺(持续15天)使大鼠对苯丙胺诱导的运动刺激产生敏感化。用5-HT前体L-5-羟色氨酸(5-HTP;腹腔注射25毫克/千克)进行急性预处理或用选择性5-HT再摄取抑制剂西酞普兰(皮下注射5.0毫克/千克,每日两次)进行慢性治疗,均未改变苯丙胺诱导的运动敏感化的表达。在高架十字迷宫中,接受重复苯丙胺治疗的动物在接触苯丙胺(皮下注射1.0毫克/千克;-35分钟)后表现出行为去抑制,急性5-HTP和慢性西酞普兰治疗均可拮抗这种现象。总之,这些发现表明,对苯丙胺的行为敏感化与苯丙胺诱导的行为去抑制有关,急性5-HTP以及慢性西酞普兰治疗可抵消苯丙胺诱导的行为去抑制的表达,但不能抵消运动敏感化。5-HTP和西酞普兰对行为去抑制的拮抗作用似乎源于药物诱导的脑5-HT神经传递的促进作用。

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