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氟哌啶醇对苯丙胺和哌甲酯诱导的条件性位置偏爱及运动活性的影响。

The effects of haloperidol on amphetamine- and methylphenidate-induced conditioned place preferences and locomotor activity.

作者信息

Mithani S, Martin-Iverson M T, Phillips A G, Fibiger H C

出版信息

Psychopharmacology (Berl). 1986;90(2):247-52. doi: 10.1007/BF00181251.

Abstract

Place preferences induced by the indirect dopamine (DA) receptor agonists amphetamine (AMP) and methylphenidate (MPD) were investigated using an unbiased compartment procedure. In this procedure, prior to drug conditioning, rats did not exhibit preferences for either of the two compartments in a shuttle box. Both stimulants produced place preferences. Repeated testing of the MPD conditioned animals revealed an extinction-like decrease in preferences, suggesting that place preferences produced by MPD result from conditioning of MPD's reinforcing properties to environmental cues. During conditioning, the DA receptor antagonist haloperidol was administered prior to drug (S+) treatments, or prior to both drug and vehicle (S-) treatments. Haloperidol pretreatment blocked place preferences induced by AMP but not by MPD. In contrast, haloperidol blocked locomotor activity stimulated by either AMP or MPD. These results suggest that the reinforcing properties of MPD and AMP may be mediated by different mechanisms, while the locomotor stimulant effects of the two drugs have common neural substrates.

摘要

采用无偏隔室程序研究了间接多巴胺(DA)受体激动剂苯丙胺(AMP)和哌醋甲酯(MPD)诱导的位置偏爱。在此程序中,在药物条件训练之前,大鼠在穿梭箱中对两个隔室均未表现出偏爱。两种兴奋剂均产生了位置偏爱。对经MPD条件训练的动物进行重复测试发现,偏爱出现了类似消退的下降,这表明MPD产生的位置偏爱是由于MPD的强化特性与环境线索形成条件反射所致。在条件训练期间,在给予药物(S +)处理之前,或在给予药物和溶剂(S-)处理之前,给予DA受体拮抗剂氟哌啶醇。氟哌啶醇预处理可阻断AMP诱导的位置偏爱,但不能阻断MPD诱导的位置偏爱。相反,氟哌啶醇可阻断由AMP或MPD刺激引起的运动活动。这些结果表明,MPD和AMP的强化特性可能由不同机制介导,而两种药物的运动刺激作用具有共同的神经基础。

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