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首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >A comparative study of the antidepressant effect of ondansetron and granisetron on Albino mice
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A comparative study of the antidepressant effect of ondansetron and granisetron on Albino mice

机译:恩丹西酮和格拉司琼对白化病小鼠抗抑郁作用的比较研究

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Background: Ondansetron and granisetron are selective 5-HT receptor antagonists used as antiemetics. The present study as aimed at comparing the antidepressant activity of ondansetron and granisetron in animal experimental models. Methods: The study was done after obtaining approval from the institutional animal ethical committee of JJM Medical college, Davangere and CPCSEA. A total of 24 mice of either sex and of weight between 20-40g were included in the study. The antidepressant activity of ondansetron and granisetron was evaluated in mice using forced swim test model (FST) and tail suspension test model (TST). In both the experimental models animals were divided into 4 groups and received the following drugs- Group 1 (control) - normal saline 10mg/kg i.p, Group 2 (standard)-fluoxetine 10mg/kg i.p, Group 3(test drug 1), ondansetron 2mg/kg i.p, Group 4 (test drug 2)- granisetron 0.5mg/kg i.p. The duration of immobility was noted and compared amongst the 4 groups in both the models 60 min after drug administration. The observations were analysed using ANOVA (one way) and post hoc Tukey’s test. Results: The test drugs showed significant reduction in duration of immobility in both the models. In FST and TST models, granisetron (0.5mg/kg i.p) showed a significant reduction in immobility period of 10.33 sec and 67 secs respectively when compared to ondansetron (2mg/kg i.p) and the standard drug fluoxetine (10mg/kg i.p). Conclusions: The results of study suggest that granisetron may be useful as a potential candidate for treatment of depression. Hence further animal studies with different model for depression and clinical studies should be conducted in order to choose the better drug for treatment PONV which is often associated with depression.
机译:背景:恩丹西酮和格拉司琼是用作止吐药的选择性5-HT受体拮抗剂。本研究旨在比较恩丹西酮和格拉司琼在动物实验模型中的抗抑郁活性。方法:本研究在获得JJM医学院,Davangere和CPCSEA的机构动物伦理委员会批准后进行。该研究共包括24只性别或体重在20-40g之间的小鼠。使用强迫游泳试验模型(FST)和尾部悬浮试验模型(TST)在小鼠中评估了昂丹司琼和Granisetron的抗抑郁活性。在这两个实验模型中,动物均分为4组,分别接受以下药物:第1组(对照组)-生理盐水10mg / kg ip,第2组(标准)-氟西汀10mg / kg ip,第3组(测试药物1),恩丹西酮2mg / kg ip,第4组(试验药物2)-格拉司琼0.5mg / kg ip在给药后60分钟,记录并比较两个模型中4组之间的不动时间。使用ANOVA(单向)和事后Tukey检验对观察结果进行了分析。结果:在两种模型中,测试药物的固定时间均显着减少。在FST和TST模型中,与昂丹西酮(2mg / kg i.p)和标准药物氟西汀(10mg / kg i.p)相比,格拉司琼(0.5mg / kg i.p)的固定期显着减少,分别为10.33秒和67秒。结论:研究结果表明,格拉司琼可能作为治疗抑郁症的潜在候选者。因此,应该选择具有不同模型的抑郁症进行进一步的动物研究,并进行临床研究,以便选择更好的药物来治疗常常与抑郁症相关的PONV。

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