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首页> 外文期刊>Neurochemical Research >Protective Effects of Lamotrigine, Aripiprazole and Escitalopram on Depression-induced Oxidative Stress in Rat Brain
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Protective Effects of Lamotrigine, Aripiprazole and Escitalopram on Depression-induced Oxidative Stress in Rat Brain

机译:拉莫三嗪,阿立哌唑和依西酞普兰对抑郁症诱导的大鼠脑氧化应激的保护作用

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摘要

We investigated the effects of lamotrigine, aripiprazole and escitalopram administration and experimental depression on lipid peroxidation (LP) and antioxidant levels in cortex of the brain in rats. Forty male wistar rats were randomly divided into five groups. First group was used as control although second group was depression-induced group. Aripiprazole, lamotrigine and escitalopram per day were orally supplemented to chronic mild stress (CMS) depression-induced rats constituting the third, fourth and fifth groups for 28 days, respectively. Depression resulted in significant decrease in the glutathione peroxidase (GSH-Px) activity, reduced glutathione and vitamin C of cortex of the brain although their levels and beta-carotene concentrations were increased by the three drugs administrations to the animals of CMS induced depression group. The LP levels in the cortex of the brain and plasma of depression group were elevated although their levels were decreased by the administrations. The increases of antioxidant values in lamotrigine group were higher according to aripiprazole and escitalopram supplemented groups. Vitamin A level did not change in the five groups. In conclusion, the experimental depression is associated with elevated oxidative stress although treatment with lamotrigine has most protective effects on the oxidative stress within three medicines.
机译:我们调查了拉莫三嗪,阿立哌唑和依他普仑的给药以及实验性抑郁症对大鼠大脑皮层脂质过氧化(LP)和抗氧化水平的影响。将四十只雄性Wistar大鼠随机分为五组。尽管第二组是抑郁症诱发的组,但第一组用作对照。每天向组成第三,第四和第五组的慢性轻度应激(CMS)抑郁诱导的大鼠口服阿立哌唑,拉莫三嗪和依他普仑,分别持续28天。抑郁导致CMS诱导的抑郁症组动物服用三种药物,谷胱甘肽过氧化物酶(GSH-Px)活性显着降低,谷胱甘肽和大脑皮质的维生素C降低,尽管它们的水平和β-胡萝卜素浓度增加。抑郁组的大脑皮质和血浆中的LP水平升高,尽管通过施用降低了它们的水平。补充阿立哌唑和依西酞普兰的组中,拉莫三嗪组抗氧化值的增加较高。五组中的维生素A水平没有变化。总之,尽管拉莫三嗪治疗对三种药物中的氧化应激具有最大的保护作用,但实验性抑郁症与氧化应激升高有关。

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