Antidepressant like activity of Buspirone but not ondensetron in combination with Fluoxetine or Desipramine in mice

V. Verma, Biswadeep Banerjee, A. Mehta
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Abstract

Background: The involvement of one or more 5-HT receptor sub-types in the pathophysiology of depression is still unclear. The study was performed to investigate the effect of ondansetron and buspirone on depression, and their interaction with fluoxetine or desipramine.Methods: The mice were administered ondansetron, buspirone alone and in combinations with fluoxetine or desipramine for 21 days, and the antidepressant effect was assessed by the immobility period and the sucrose consumption, on the tail suspension test (TST) and the chronic mild stress (CMS) models, respectively.Results: Both ondansetron and buspirone when given alone demonstrated slight non-significant decrease in the immobility time. Ondensetron when given in combination with fluoxetine (10 mg/kg; i.p.) and desipramine (15 mg/kg; i.p.), showed significant decrease in immobility time in comparison to the control group only. On the other hand, both the combinations of buspirone, either with fluoxetine or desipramine showed significant decrease in the immobility time when compared to the respective group. In CMS, the fluoxetine, desipramine, ondansetron, and buspirone showed gradual increase in the sucrose consumption, at the end of 4th, 5th, and 6th week, but the significant effect was observed only at the end of 6th week, as compared to the control. The combination of buspirone with desipramine but not with fluoxetine showed significant increase in sucrose consumption when compared to respective group.Conclusions: Therefore, the study indicates that both buspirone and ondansetron have a potential antidepressant like action, although buspirone has shown better antidepressant activity than ondansetron as observed in various combination groups.
丁螺环酮与氟西汀或地西帕明联合在小鼠体内具有抗抑郁活性,而非致密司琼
背景:一种或多种5-HT受体亚型参与抑郁症的病理生理尚不清楚。本研究旨在探讨昂丹司琼和丁螺环酮对抑郁症的影响,以及它们与氟西汀或地西帕明的相互作用。方法:小鼠单用昂丹司琼、丁螺环酮及与氟西汀、地西帕明联合给药21 d,分别采用悬尾试验(TST)和慢性轻度应激(CMS)模型,以静止时间和蔗糖消耗量评价其抗抑郁效果。结果:单独给药昂丹司琼和丁螺环酮均能明显减少静止时间。奥登司琼与氟西汀合用时(10mg /kg;静脉滴注)和地西帕明(15mg /kg;i.p.),与对照组相比,静止时间显着减少。另一方面,丁螺环酮与氟西汀或地西帕明的两种组合相比,各自组的固定时间均显着减少。在CMS组中,氟西汀、地西帕明、昂丹司琼和丁螺环酮在第4、5、6周末蔗糖消耗量逐渐增加,但仅在第6周末与对照组相比才有显著效果。丁螺环酮与地西帕明联合使用而不与氟西汀联合使用时,与各自组相比,蔗糖消耗量显著增加。结论:本研究提示丁螺环酮和昂丹司琼均具有潜在的类抗抑郁作用,尽管在各联合组中观察到丁螺环酮表现出比昂丹司琼更好的抗抑郁活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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