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Role of Aspirin and Dexamethasone against Experimentally Induced Depression in Rats

机译:阿司匹林和地塞米松对大鼠实验性抑郁的作用

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摘要

A large number of current studies indicate that inflammatory mediators may contribute to depression in experimental models as well as in human beings. Nevertheless, the subject, whether anti-inflammatory treatments can prevent depression still remains controversial. In the present study, a chronic mild stress (CMS) model of male Sprague Dawley rats was used to investigate the role of anti-inflammatory drugs in the treatment of depression. All the animals in different groups, except the normal control group, were exposed to CMS procedure for 28 days and concurrently treated with aspirin (10 mg/kg, p.o.), dexamethasone (1 mg/kg p.o.) and amitriptyline (10 mg/kg p.o., reference standard), respectively. Amitriptyline was also used in combination with aspirin and dexamethasone to inspect any synergistic effects. Tests performed towards the end of the study included sucrose preference test, behavioural tests like forced swim test, elevated plus-maze, light/dark box, locomotor activity and biochemical estimations like serum cortisol and brain neurotransmitters. Disease control group (CMS-treated) produced significant depressive behaviour in rats. The animals treated with aspirin showed increased sucrose preference, decreased immobility time in forced swim test, decreased serum cortisol and increased brain serotonin levels signifying antidepressant action. In contrast, there was aggravation of depressive behaviour in rats treated with dexamethasone. Together, these findings suggest that aspirin can serve as a potential antidepressant both individually and as adjunctive agent in the treatment of depression. Inhibition of the inflammatory mediators during stress procedures or any other potential physiological and biochemical mechanisms may be involved in its antidepressant effect.
机译:当前的大量研究表明,炎症介质可能在实验模型以及人类中导致抑郁。然而,该受试者是否使用抗炎药可以预防抑郁症仍存在争议。在本研究中,使用雄性Sprague Dawley大鼠的慢性轻度应激(CMS)模型研究抗炎药在治疗抑郁症中的作用。除正常对照组外,不同组中的所有动物均暴露于CMS程序28天,并同时接受阿司匹林(10 mg / kg,口服),地塞米松(1 mg / kg口服)和阿米替林(10 mg / kg)处理po,参考标准)。阿米替林还与阿司匹林和地塞米松联合使用以检查任何协同作用。在研究结束时进行的测试包括蔗糖偏爱测试,行为测试(如强迫游泳测试),高迷宫测试,明/暗盒,运动活动以及生化评估(如血清皮质醇和脑神经递质)。疾病对照组(经CMS处理)在大鼠中产生了明显的抑郁行为。用阿司匹林治疗的动物表现出增加的蔗糖偏爱性,在强迫游泳试验中减少的不动时间,减少的血清皮质醇和增加的脑5-羟色胺水平,表明抗抑郁作用。相反,地塞米松治疗的大鼠的抑郁行为有所加重。这些发现共同表明,阿司匹林既可以单独用作潜在的抗抑郁药,又可以作为治疗抑郁症的辅助剂。在应激过程中抑制炎症介质或任何其他潜在的生理和生化机制可能与其抗抑郁作用有关。

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