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Effect of Metformin and Sitagliptin on Doxorubicin-Induced Cardiotoxicity in Rats: Impact of Oxidative Stress Inflammation and Apoptosis

机译:二甲双胍和西他列汀对阿霉素诱导的大鼠心脏毒性的影响:氧化应激炎症和细胞凋亡的影响。

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摘要

Doxorubicin (DOX) is a widely used antineoplastic drug whose efficacy is limited by its cardiotoxicity. The aim of this study was to investigate the possible protective role of the antidiabetic drugs metformin (250 mg/kg dissolved in DW p.o. for seven days) and sitagliptin (10 mg/kg dissolved in DW p.o. for seven days) in a model of DOX-induced (single dose 15 mg/kg i.p. at the fifth day) cardiotoxicity in rats. Results of our study revealed that pretreatment with metformin or sitagliptin produced significant (P < 0.05) cardiac protection manifested by a significant decrease in serum levels of LDH and CK-MB enzymes and cardiac MDA and total nitrites and nitrates levels, a significant increase in cardiac SOD activity, and remarkable improvement in the histopathological features as well as a significant reduction in the immunohistochemical expression of COX-2, iNOS, and caspase-3 enzymes as compared to DOX group. These results may suggest using metformin and/or sitagliptin as preferable drugs for diabetic patients suffering from cancer and receiving DOX in their chemotherapy regimen.
机译:阿霉素(DOX)是一种广泛使用的抗肿瘤药,其疗效受到心脏毒性的限制。这项研究的目的是在DOX模型中研究抗糖尿病药物二甲双胍(250μg/ kg溶于DW po 7天)和西他列汀(10μmg/ kg溶于DW po 7天)的可能的保护作用。诱导的大鼠(第五天单剂量15μmg/ kg ip)心脏毒性。我们的研究结果表明,用二甲双胍或西他列汀进行预处理可产生显着的(P <0.05)心脏保护作用,其表现为血清LDH和CK-MB酶水平,心脏MDA和总亚硝酸盐和硝酸盐水平显着降低,而心脏的显着增加与DOX组相比,SOD活性,组织病理学特征显着改善以及COX-2,iNOS和caspase-3酶的免疫组织化学表达显着降低。这些结果可能建议使用二甲双胍和/或西他列汀作为患有癌症并在其化疗方案中接受DOX的糖尿病患者的优选药物。

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