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大鼠外侧隔区组胺能系统对焦虑样行为的调节作用

Histaminergic system of the lateral septum in the modulation of anxiety-like behaviour in rats.

作者信息

Zarrindast Mohammad-Reza, Valizadegan Farhad, Rostami Parvin, Rezayof Ameneh

机构信息

Department of Pharmacology and Iranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Eur J Pharmacol. 2008 Mar 31;583(1):108-14. doi: 10.1016/j.ejphar.2008.01.003. Epub 2008 Jan 26.

Abstract

The central histaminergic system is known to have modulatory influence on anxiety-related behaviour both in animals and humans through histamine H1 and/or H2 receptors. In the present study, the effects of intra-lateral septal microinjections of histaminergic agents on anxiety-related behaviours in male Wistar rats have been investigated. As a model of anxiety, the elevated plus-maze which is a useful test to investigate the effects of anxiogenic or anxiolytic drugs in rodents was used. Intra-lateral septal administration of histamine (0.5 and 1 microg/rat) decreased the percentage of open arm entries and open arm time but not locomotor activity, showing an anxiogenic response. The intra-lateral septal injections of different doses of the histamine H1 receptor antagonist, pyrilamine (5, 10 and 20 microg/rat) or the histamine H2 receptor antagonist, ranitidine (5, 10 and 20 microg/rat) could not significantly alter the anxiety-like parameters in the plus-maze test. However, intra-lateral septal injections of different doses of pyrilamine (10 and 20 microg/rat) or ranitidine (10 and 20 microg/rat) significantly reversed histamine (1 microg/rat)-induced anxiogenic effect. The results may indicate that the histaminergic system of lateral septum modulate anxiety-like behaviour through histamine H1 and H2 receptors.

摘要

已知中枢组胺能系统通过组胺H1和/或H2受体对动物和人类的焦虑相关行为具有调节作用。在本研究中,已对雄性Wistar大鼠进行了侧脑室间隔微量注射组胺能药物对焦虑相关行为影响的研究。作为焦虑模型,使用了高架十字迷宫,这是一种用于研究致焦虑或抗焦虑药物对啮齿动物影响的有用测试。侧脑室间隔注射组胺(0.5和1微克/只大鼠)降低了进入开放臂的百分比和在开放臂停留的时间,但不影响运动活性,显示出致焦虑反应。侧脑室间隔注射不同剂量的组胺H1受体拮抗剂吡苄明(5、10和20微克/只大鼠)或组胺H2受体拮抗剂雷尼替丁(5、10和20微克/只大鼠)在十字迷宫试验中不能显著改变焦虑样参数。然而,侧脑室间隔注射不同剂量的吡苄明(10和20微克/只大鼠)或雷尼替丁(10和20微克/只大鼠)可显著逆转组胺(1微克/只大鼠)诱导的致焦虑作用。结果可能表明,侧脑室间隔的组胺能系统通过组胺H1和H2受体调节焦虑样行为。

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