在雄性和雌性C57BL/6J小鼠的强迫游泳试验中,雷替加宾促进氯胺酮的抗抑郁作用。

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Yixue Qin , Haoxuan Li , Yuqi Zhang , Jun-Li Cao , Wenxin Zhang , Hongxing Zhang
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引用次数: 0

摘要

氯胺酮在特定的临床环境中越来越多地被用作一种快速起效的抗抑郁药。然而,作为一种迷幻试剂,其潜在的生理和心理依赖性限制了其临床应用。在此,我们在雄性和雌性C57BL/6J小鼠的强迫游泳试验中,添加了一种KCNQ通道开放剂retigabine作为辅助治疗,以观察其对氯胺酮抗抑郁特性的影响。行为数据表明,在强迫游泳试验中,腹膜内注射氯胺酮对动物的不动性能表现出剂量依赖性影响。在用相对较低剂量的氯胺酮治疗的小鼠中,添加雷替加宾足以诱导显著的抗抑郁作用,单独给药时氯胺酮不能起到抗抑郁作用。当同时给予瑞加宾时,氯胺酮在强迫游泳试验中的抗抑郁作用显著增强,有效时间延长。总之,雄性和雌性小鼠的这些结果表明,雷替加宾的辅助治疗是促进氯胺酮抗抑郁作用的一种替代方案,因此有可能遇到其可能的生理和心理依赖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Retigabine promotes ketamine's antidepressant effect in the forced swim test in male and female C57BL/6J mice

Ketamine has been increasingly used as a rapid-onset antidepressant in specific clinical settings. However, as a psychedelic reagent, the potential of physical and psychological dependence limits its clinical use. Here, we added retigabine, a KCNQ channel opener, as an adjunctive treatment to observe its effect on ketamine's antidepressant property in a forced swim test in both male and female C57BL/6 J mice. Behavioral data demonstrated that intraperitoneal injection of ketamine exhibited a dose-dependent effect on animals' immobility performance in the forced swim test. Adding retigabine was sufficient to induce a remarkable antidepressant effect in mice treated with a relatively lower dose of ketamine which failed to be antidepressant when administrated separately. When simultaneously gave retigabine, ketamine's antidepressant effect in the forced swim test was significantly enhanced with a prolonged effective duration. Together, these results from both male and female mice indicated that adjunctive treatment with retigabine was an alternative to promote the antidepressant effect of ketamine, thus holding the possibility of encountering its possible physical and psychological dependence.

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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 Purely biochemical or toxicology studies will not be published.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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