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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Behavioural effects in mice of subchronic buspirone, ondansetron and tianeptine. II. The elevated plus-maze.
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Behavioural effects in mice of subchronic buspirone, ondansetron and tianeptine. II. The elevated plus-maze.

机译:亚慢性丁螺环酮,恩丹西酮和替尼汀对小鼠的行为影响。二。高架的迷宫。

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In follow-up to recent work on benzodiazepines (chlordiazepoxide) and selective monoamine reuptake inhibitors (maprotiline and fluvoxamine), the present study compares the effects of the 5-HT1A receptor partial agonist, buspirone (0.75-3.0 mg/kg), the 5-HT3 receptor antagonist, ondansetron (0.1-100 micrograms/kg), and the novel antidepressant, tianeptine (2.5-10.0 mg/kg), on the behaviour of mice in the elevated plus-maze test of anxiety. Compounds were administered daily for 21 days prior to testing, and an ethological scoring technique was used to generate comprehensive behavioural profiles. Results show that subchronic treatment with ondansetron failed to influence the behaviour of mice in the plus-maze, while the limited changes induced by buspirone could not be attributed to anxiety-related processes. In contrast, tianeptine produced unambiguous anxiogenic-like effects at the top dose tested (10.0 mg/kg), a profile that was not secondary to changes in general levels of locomotor activity or exploration. Data are discussed in relation to current pharmacotherapy of anxiety and depressive disorders, and the nature of anxiety induced by animal models.
机译:在对苯二氮卓类药物(氯二氮卓)和选择性单胺再摄取抑制剂(马普替林和氟伏沙明)的最新研究的后续研究中,本研究比较了5-HT1A受体部分激动剂丁螺环酮(0.75-3.0 mg / kg),5 -HT3受体拮抗剂恩丹西酮(0.1-100微克/千克)和新型抗抑郁药天肽(2.5-10.0毫克/千克)对高迷宫焦虑症小鼠行为的影响。在测试之前,化合物每天给药21天,然后使用一种行为学评分技术生成全面的行为特征。结果表明,使用恩丹西酮的亚慢性治疗不能影响正迷宫中小鼠的行为,而丁螺环酮诱导的有限变化不能归因于焦虑相关过程。相比之下,替丁汀在最高测试剂量(10.0 mg / kg)下产生了明确的类似焦虑的作用,这一特征并不随运动活动或探索的一般水平的变化而变化。讨论了与当前焦虑和抑郁症药物疗法以及动物模型引起的焦虑性质有关的数据。

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