利眠宁(Chlordiazepoxide)可减少青少年小鼠高架迷宫中的焦虑样行为:药理验证研究

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Anapaula Themann, Minerva Rodriguez, Joselynn Reyes-Arce, Sergio D. Iñiguez
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引用次数: 0

摘要

本报告评估了氯地西泮对幼鼠高架迷宫(EPM)表现的影响,氯地西泮是一种苯二氮卓类药物,通常用于治疗青少年/儿童焦虑症。之所以采用这种方法,是因为氯氮卓在成年啮齿类动物的多种模型中都能产生类似抗焦虑的效果,但对这种苯二氮卓在幼鼠中的行为影响却知之甚少。因此,我们对出生后第35天的雄性C57BL/6小鼠腹腔注射一次氯氮卓(0、5或10毫克/千克)。30分钟后,让小鼠探索EPM 5分钟。我们发现,经氯地西泮(5毫克/千克和10毫克/千克)处理的小鼠在EPM的开放臂上探索的时间更长。两组小鼠的探索速度(厘米/秒)和距离(厘米)均无差异。这些结果表明,氯氮卓可诱导青春期雄性小鼠产生抗焦虑相关行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chlordiazepoxide reduces anxiety-like behavior in the adolescent mouse elevated plus maze: A pharmacological validation study

This report evaluates the effects of chlordiazepoxide, a benzodiazepine commonly prescribed to manage anxiety-related disorders in adolescent/pediatric populations, on elevated plus maze (EPM) performance in juvenile mice. This approach was taken because chlordiazepoxide produces anxiolytic-like effects in multiple models in adult rodents, however, less is known about the behavioral effects of this benzodiazepine in juveniles. Thus, we administered a single intraperitoneal injection of chlordiazepoxide (0, 5, or 10 mg/kg) to postnatal day 35 male C57BL/6 mice. Thirty minutes later, mice were allowed to explore the EPM for 5-min. We found that chlordiazepoxide-treated mice (5 and 10 mg/kg) spent more time exploring the open arms of the EPM. No differences in velocity (cm/s) or distance traveled (cm) were observed between the groups. These results indicate that chlordiazepoxide induces anxiolytic-related behavior in adolescent male mice.

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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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