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大鼠焦虑改良社交互动模型的药理学特征

Pharmacological characterisation of a modified social interaction model of anxiety in the rat.

作者信息

Guy A P, Gardner C R

出版信息

Neuropsychobiology. 1985;13(4):194-200. doi: 10.1159/000118187.

Abstract

Social interaction (SI) between two unfamiliar male rats in a dimly lit, familiar environment has been investigated as a model of anxiety, where novelty of the partner remains as the principal anxiogenic stimulus. A range of centrally acting drugs have been tested in this situation. Chlordiazepoxide, nitrazepam, flunitrazepam, and flurazepam all increase SI, as does buspirone, CL 218872, suriclone, sodium valproate, and nicotinamide in the model described. Anxiogenic agents FG 7142 and yohimbine reduced SI without significant modification of motor activities. However, the stimulant amphetamine increased all behaviours in this condition. Amphetamine also increased all behaviours when rats were tested with their cagemates, when the desire for SI is largely satiated. CL 218872 also increased SI in this second situation, and it is suggested that this agent may have a non-specific component in its action in this test. Additionally, caffeine, theophylline, and piracetam may also have non-specific behavioural actions in this model.

摘要

在光线昏暗的熟悉环境中,对两只陌生雄性大鼠之间的社交互动(SI)进行了研究,以此作为焦虑模型,其中伙伴的新奇性仍是主要的致焦虑刺激因素。已经在这种情况下测试了一系列中枢作用药物。在所述模型中,氯氮卓、硝西泮、氟硝西泮和氟西泮均能增加社交互动,丁螺环酮、CL 218872、舒立克隆、丙戊酸钠和烟酰胺也有此作用。致焦虑剂FG 7142和育亨宾可减少社交互动,而对运动活动无明显影响。然而,兴奋剂苯丙胺在这种情况下会增加所有行为。当大鼠与同笼伙伴进行测试时,苯丙胺也会增加所有行为,此时对社交互动的需求在很大程度上已得到满足。CL 218872在第二种情况下也会增加社交互动,有人认为该药物在该测试中的作用可能有非特异性成分。此外,咖啡因、茶碱和吡拉西坦在该模型中可能也有非特异性行为作用。

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