心氧烷和硒对大鼠脑和心脏脂质过氧化及多巴胺水平的影响

D. C. Guzmán, N. O. Brizuela, G. B. Mejía, H. Olguín, L. S. Reyes, Armando Valenzuela Pereza, N. L. Ruíz, D. S. Angel
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摘要

背景:Cardioxane已被用于晚期恶性肿瘤患者的心脏保护。硒是人体必需的微量元素,具有抗氧化等多种功能。本研究旨在探讨心氧烷(CDX)和硒(Se)对脑和心脏是否具有加性抗氧化保护作用,及其与多巴胺水平的关系。方法:雄性Wistar大鼠36只,每组6只,治疗方法为:G1,生理盐水溶液0.9%(对照组);G2, CDX 100 mg/kg;G3, 60 μg/kg硒;G4、3-硝基丙酸(3NP) 20 mg/kg;G5, 3NP + CDX和G6, 3NP + Se. 3NP作为氧化应激诱导剂。腹腔给药5天。在治疗的最后一天处死动物,提取大脑和心脏,测定脂质过氧化、多巴胺、谷胱甘肽(GSH)、atp酶、钙和H2O2。结果:G2和G5大鼠大脑皮层和纹状体多巴胺减少,心脏、大脑皮层和小脑/延髓GSH升高。2、3、5、6组大鼠心脏和皮质atp酶活性升高。3NP处理动物的皮质脂质过氧化和H2O2增加。结论:CDX增加了大脑和心脏的抗氧化能力,而硒则通过3NP产生自由基的能力来促进多巴胺代谢的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Cardioxane and Selenium on Lipoperoxidation and Levels of Dopamine in Rat Brain and Heart
Background: Cardioxane has been probed in patients with advanced malignancies to protect the heart. Selenium, an essential micronutrient exerts varieties of functions such as antioxidant. The aim of this study was to test if cardioxane (CDX) and selenium (Se) have additive antioxidant protective effect on brain and heart, and their relation with dopamine levels. Methods: Thirty-six male Wistar rats divided in groups of 6 animals each, were treated as follows: G1, saline solution 0.9% (control); G2, 100 mg/kg of CDX; G3, 60 μg/kg of Se; G4, 20 mg/kg of 3-nitropropionic acid (3NP); G5, 3NP + CDX and G6, 3NP + Se. 3NP was used as an oxidative stress inducer. Drugs were administered intraperitoneally for 5 days. The animals were sacrificed on the last day of treatment and the brain and heart were extracted and used to measure lipid peroxidation, dopamine, glutathione (GSH), ATPase, calcium, and H2O2. Results: In G2 and G5, dopamine decreased in cortex and striatum while GSH increased in heart, cortex and cerebellum/medulla oblongata. ATPase activity increased in heart and cortex of groups 2, 3, 5 and 6. Lipoperoxidation and H2O2 increased in cortex of animals treated with 3NP. Conclusion: These results suggest that CDX increases antioxidant capacity in the brain and heart while selenium promotes alteration in dopamine metabolism in view of the capacity of 3NP to generate free radicals.
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