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首页> 外文期刊>Pharmacological reports: PR >Enhancement of the anti-immobility action of antidepressants by risperidone in the forced swimming test in mice
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Enhancement of the anti-immobility action of antidepressants by risperidone in the forced swimming test in mice

机译:利培酮在小鼠强制游泳试验中提高抗抑郁药的抗抗抗抗性作用

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The aim of the present study was to examine the effect of antidepressants (ADs) belonging to different pharmacological groups and risperidone (an atypical antipsychotic drug), given separately or jointly, on immobility time in the forced swimming test in male C57BL/6J mice. The antidepressants: citalopram, fluvoxamine, sertraline, reboxetine, milnacipran (5 and 10 mg/kg), or risperidone in low doses (0.05 and 0.1 mg/kg) given alone did not change the immobility time ofmice in the forced swimming test. Co-treatment with reboxetine or milnacipran (10 mg/kg) and risperidone in a lower dose of 0.05 mg/kg or with sertraline, reboxetine (5 and 10 mg/kg), citalopram, fluvoxamine, milnacipran (10 mg/kg) and risperidone in a higher dose of 0.1 mg/kg produced antidepressant- like effect in the forced swimming test.WAY100635 (a 5-HT 1A receptor antagonist) inhibited the effects induced by coadministration of ADs and risperidone. Active behavior in the forced swimming test was not a consequence of an increased general activity, since the combined treatment with ADs and risperidone failed to enhance the locomotor activity of mice. The obtained results indicate that a low dose of risperidone enhances the activity of ADs in an animal model of depression, and that, among other mechanisms, 5-HT 1A receptors may play a role in these effects.
机译:本研究的目的是检测属于不同药理学基团的抗抑郁药物(ADS)和立体酮(非典型抗精神病药)的影响,单独或共同给出,对雄性C57BL / 6J小鼠的强迫游泳试验中的不可动脉时间。抗抑郁药:单独给予的低剂量(0.05和0.1mg / kg)的抗抑郁药:氟哌莫胺,塞拉葡萄酒,雷布葡萄酒,米兰哌啶素(5和10mg / kg)在强制游泳试验中没有改变造成的不动度时间。用Reboxetine或MilnaCipran(10mg / kg)和氯化酮的含量为0.05mg / kg或塞拉司胺,再甲酰胺(5和10mg / kg),西酞普兰,氟戊胺,MilnaCipran(10 mg / kg)和林蛙在强制游泳试验中产生0.1 mg / kg的抗抑郁效果较高剂量的抗抑郁效果(5-HT 1A受体拮抗剂)抑制了ADS和Risperidone的共同诱导的作用。强制游泳试验中的活性行为不是一般性活性增加的结果,因为与ADS和Risperidone的结合治疗未能增强小鼠的运动活性。所得结果表明,低剂量的立酮增强了抑郁症的动物模型中的广告的活性,并且在其他机制中,5-HT 1A受体可能在这些效果中发挥作用。

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