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大鼠的新奇诱导位置偏爱行为:阿片类药物和多巴胺能药物的作用

Novelty-induced place preference behavior in rats: effects of opiate and dopaminergic drugs.

作者信息

Bardo M T, Neisewander J L, Pierce R C

机构信息

Department of Psychology, University of Kentucky, Lexington 40506.

出版信息

Pharmacol Biochem Behav. 1989 Mar;32(3):683-9. doi: 10.1016/0091-3057(89)90018-x.

Abstract

In Experiment 1, adult male rats were given eight 30-min exposures to one of two distinct environments. Control animals received either four exposures to each environment or were not exposed to either environment. When given free-choice access to both environments simultaneously, animals spent significantly more time in the novel environment relative to the familiar environment. In these same animals, horizontal and vertical activity rates were lower in the novel environment than in the familiar environment. In Experiments 2-5, animals were assessed for novelty preference behavior under the influence of either morphine (0, 0.1, 0.3, 1.0 or 3.0 mg/kg), naltrexone (0, 0.1, 0.3 or 1.0 mg/kg), amphetamine (0, 0.1, 0.3 or 1.0 mg/kg) or haloperidol (0, 0.03, 0.1, 0.3 or 1.0 mg/kg). Haloperidol produced a dose-dependent disruption in novelty preference behavior, while all other drugs tested were without effect. Haloperidol also disrupted the novelty-induced decrease in horizontal and vertical activity rates. These results suggest that haloperidol blocks the reinforcing and locomotor-depressant effects of a novel environment in a free-choice preference test.

摘要

在实验1中,成年雄性大鼠在两种不同环境之一中接受了八次每次30分钟的暴露。对照动物对每种环境各接受四次暴露,或者不暴露于任何一种环境。当给予动物同时自由选择进入两种环境的机会时,相对于熟悉环境,动物在新环境中花费的时间显著更多。在这些相同的动物中,新环境中的水平和垂直活动率低于熟悉环境。在实验2至5中,评估动物在吗啡(0、0.1、0.3、1.0或3.0毫克/千克)、纳曲酮(0、0.1、0.3或1.0毫克/千克)、苯丙胺(0、0.1、0.3或1.0毫克/千克)或氟哌啶醇(0、0.03、0.1、0.3或1.0毫克/千克)影响下的新奇偏好行为。氟哌啶醇对新奇偏好行为产生剂量依赖性破坏,而测试的所有其他药物均无作用。氟哌啶醇还破坏了新奇诱导的水平和垂直活动率的降低。这些结果表明,在自由选择偏好测试中,氟哌啶醇阻断了新环境的强化和运动抑制作用。

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