首页> 外文期刊>International Journal of Pharmacology >Losartan and/or Naringenin Ameliorates Doxorubicin Induced Cardiac, Hepatic and Renal Toxicities in Rats
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Losartan and/or Naringenin Ameliorates Doxorubicin Induced Cardiac, Hepatic and Renal Toxicities in Rats

机译:氯沙坦和/或柚皮苷可减轻阿霉素诱导的大鼠的心脏,肝和肾毒性

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Background and Objective: Doxorubicin (DOX) is conventional chemotherapy for several types of malignancies although it induces considerable oxidative damage in different physiological systems. The present study aimed to examine whether the co-administration of naringenin (NG) and losartan (LOS) can produce additional protective effects against DOX-induced cardiac, hepatic and renal toxicities in rats. Materials and Methods: The LT and/or NG 2 week’s pre-treated animals were challenged with intraperitoneal DOX (15 mg kgsup?1/sup). One week later, cardiac, hepatic and renal tissues along with serum were collected for biochemical and histopathological evaluations. Results: The altered histological architecture of the cardiac, hepatic and renal by DOX were restored by LT and NG treatments. Combining both compounds showed augmented protective effects. The LT and NG combination significantly ameliorated DOX associated elevation in serum inflammatory cytokines. In addition, DOX challenge induced cardiac, hepatic and renal toxicities along with disturbances in the biological oxidative defense capabilities manifested by elevated lipid peroxidation products, lowered glutathione levels and inhibited antioxidant enzymes activities. Co-administration of LT and NG markedly improved oxidative stress biomarkers and shifted the serum aminotransferases, creatinine, urea, lactate dehydrogenase and creatine kinases to their normal levels. Conclusion: Merging LT and NG therapies revealed significant advantages over single therapy with regards to their antioxidant and anti-inflammatory actions, which suggested a synergistic value of their combination.
机译:背景与目的:阿霉素(DOX)是用于多种类型恶性肿瘤的常规化学疗法,尽管在不同的生理系统中会引起相当大的氧化损伤。本研究旨在研究柚皮苷(NG)和氯沙坦(LOS)的共同给药是否可以产生额外的保护作用,以抵抗DOX诱导的大鼠心脏,肝脏和肾脏毒性。材料和方法:对经过2周预处理的LT和/或NG的动物进行腹膜内DOX(15 mg kg ?1 )攻击。一周后,收集心脏,肝和肾组织以及血清进行生化和组织病理学评估。结果:通过LT和NG处理可以恢复DOX改变的心脏,肝和肾的组织学结构。两种化合物的组合显示出增强的保护作用。 LT和NG组合可明显改善血清炎症细胞因子与DOX相关的升高。此外,DOX挑战诱发的心脏,肝脏和肾脏毒性,以及生物氧化防御能力的紊乱,表现为脂质过氧化产物升高,谷胱甘肽水平降低和抗氧化酶活性受到抑制。 LT和NG的共同给药可显着改善氧化应激生物标志物,并将血清氨基转移酶,肌酐,尿素,乳酸脱氢酶和肌酸激酶恢复至正常水平。结论:LT和NG疗法的合并在抗氧化和抗炎作用方面显示出优于单一疗法的显着优势,这表明它们的组合具有协同价值。

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