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首页> 外文期刊>Indian Journal of Experimental Biology >Possible role of citalopram and desipramine against sleep deprivation-induced anxiety like-behavior alterations and oxidative damage in mice
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Possible role of citalopram and desipramine against sleep deprivation-induced anxiety like-behavior alterations and oxidative damage in mice

机译:西酞普兰和地昔帕明对睡眠剥夺引起的焦虑样行为改变和小鼠氧化损伤的可能作用

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摘要

Sleep is an essential physiological process for maintaining physical, mental, and emotional health. Sleep deprivation and associated disorders like depression and anxiety are one of the major problems now-days. The present study was designed to explore the neuroprotecitve effect of citalopram and desipramine on 72 hr sleep deprivation-induced behavioral alterations and oxidative damage in mice. Various behavioral tests (plus maze, zero maze, mirror chamber, actophotometer), body weight followed by oxidative parameters (malondialdehyde level, glutathione, catalase, nitrite and protein) were assessed. Treatment with citalopram (5 and 10 mg/kg, ip) and desipramine (10 and 20 mg/kg, ip) for 5 days significantly improved locomotor activity, anti-anxiety like behavior in all paradigms tasks (mirror chamber, plus maze, zero maze) as compared to control (72 hr sleep-deprived). Biochemically, citalopram and desipramine treatment significantly restored depleted reduced glutathione, catalase activity, attenuated raised lipid peroxidation and nitrite level as compared to control (72 hr sleep-deprived) animals. Results of present study suggest that citalopram (5 and 10mg/kg, ip) and desipramine (10 and 20 mg/kg, ip) have neuroprotective effect against sleep deprivation-induced behavior alteration and oxidative damage in mice.
机译:睡眠是维持身体,心理和情绪健康的重要生理过程。睡眠剥夺和相关的疾病,如抑郁和焦虑是当今的主要问题之一。本研究旨在探讨西酞普兰和地昔帕明对小鼠72小时睡眠剥夺引起的行为改变和氧化损伤的神经保护作用。评估了各种行为测试(加上迷宫,零迷宫,镜室,光度计),体重,然后评估了氧化参数(丙二醛水平,谷胱甘肽,过氧化氢酶,亚硝酸盐和蛋白质)。西酞普兰(5和10 mg / kg,腹膜内)和地昔帕明(10和20 mg / kg,腹膜内)治疗5天可显着改善运动能力,在所有范式任务中均表现出抗焦虑之类的行为(镜室,迷宫,零迷宫)与对照(72小时睡眠不足)相比。与对照(72小时睡眠剥夺)动物相比,西酞普兰和地昔帕明治疗在生化上可显着恢复枯竭的减少的谷胱甘肽,过氧化氢酶活性,减弱的脂质过氧化和亚硝酸盐水平。目前的研究结果表明,西酞普兰(5和10mg / kg,腹腔注射)和地昔帕明(10和20mg / kg,腹腔注射)对小鼠睡眠剥夺引起的行为改变和氧化损伤具有神经保护作用。

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