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丁螺环酮对对照小鼠和应激小鼠行为的影响。

The effects of buspirone on the behaviour of control and stressed mice.

作者信息

Pokk P, Zharkovsky A

机构信息

Department of Pharmacology, University of Tartu, Estonia.

出版信息

J Physiol Pharmacol. 1998 Mar;49(1):175-85.

PMID:9594420
Abstract

The effects of buspirone on the locomotor activity and behaviour in the plus-maze and hole-board tests were studied in control and small platform stressed mice. Small platform stress for 24 hours increased the locomotor activity of mice and induced anxiolytic-like effect in the plus-maze and hole-board tests. Administration of buspirone either did not affect (2.0 and 4.0 mg/kg) or inhibited (8.0 mg/kg) locomotions in control animals. The inhibition of locomotor activity by buspirone was greater in small platform stressed mice. In control mice buspirone in doses 2.0 and 4.0 mg/kg exerted anxiolytic effect in the plus-maze and hole board test that was reflected by an increase in the percentage of entries onto and the percentage of time spent on the open arms of the plus-maze and increased number of head-dippings in the hole-board test. In contrast, in small platform stressed mice, buspirone did not induce anxiolytic action in the plus-maze and hole-board tests at any dose tested. In doses 2.0 and 4.0 mg/kg buspirone produced a sedative effect that was reflected by a decrease in the total number of entries made onto the open and into the closed arms of the plus-maze and a decrease in the number of head-dippings and rearings in the hole-board test. These data suggest that small platform stress induces a sensitization of mice to the motor depressant effect of buspirone. At the same time small platform stress induces hyposensitivity to the anxiolytic effect of buspirone. It is proposed that these changes might be due to alterations in the serotonergic transmission or to changes in the release of corticosterone.

摘要

在对照小鼠和小平台应激小鼠中研究了丁螺环酮对自发活动以及在十字迷宫和洞板试验中行为的影响。24小时的小平台应激增加了小鼠的自发活动,并在十字迷宫和洞板试验中诱导出抗焦虑样效应。给予丁螺环酮后,对照动物的自发活动要么未受影响(2.0和4.0mg/kg),要么受到抑制(8.0mg/kg)。丁螺环酮对自发活动的抑制在小平台应激小鼠中更强。在对照小鼠中,2.0和4.0mg/kg剂量的丁螺环酮在十字迷宫和洞板试验中发挥了抗焦虑作用,这表现为进入十字迷宫开放臂的百分比增加、在开放臂上花费时间的百分比增加,以及在洞板试验中头部探入次数增加。相反,在小平台应激小鼠中,丁螺环酮在任何测试剂量下均未在十字迷宫和洞板试验中诱导出抗焦虑作用。2.0和4.0mg/kg剂量的丁螺环酮产生了镇静作用,这表现为进入十字迷宫开放臂和封闭臂的总次数减少,以及在洞板试验中头部探入次数和竖毛次数减少。这些数据表明,小平台应激诱导小鼠对丁螺环酮的运动抑制作用敏感化。同时,小平台应激诱导对丁螺环酮的抗焦虑作用低敏。有人提出,这些变化可能是由于5-羟色胺能传递的改变或皮质酮释放的变化所致。

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