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Possible Protective Effect of Diacerein on Doxorubicin-Induced Nephrotoxicity in Rats

机译:双醋瑞因对阿霉素诱导的大鼠肾毒性的可能的保护作用

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摘要

Nephrotoxicity is one of the limiting factors for using doxorubicin (DOX). Interleukin 1 has major role in DOX-induced nephrotoxicity, so we investigated the effect of interleukin 1 receptor antagonist diacerein (DIA) on DOX-induced nephrotoxicity. DIA (25 and 50 mg/kg/day) was administered orally to rats for 15 days, in the presence or absence of nephrotoxicity induced by a single intraperitoneal injection of DOX (15 mg/kg) at the 11th day. We measured levels of serum urea, creatinine, renal reduced glutathione (GSH), malondialdehyde (MDA), total nitrites (NOx), catalase, and superoxide dismutase (SOD). In addition, caspase-3, tumor necrosis factor alpha (TNFα), nuclear factor kappa B (NFκB) expressions, and renal histopathology were assessed. Our results showed that DOX-induced nephrotoxicity was ameliorated or reduced by both doses of DIA, but diacerein high dose (DHD) showed more improvement than diacerein low dose (DLD). This protective effect was manifested by significant improvement in all measured parameters compared to DOX treated group by using DHD. DLD showed significant improvement of creatinine, MDA, NOx, GSH, histopathology, and immunohistochemical parameters compared to DOX treated group.
机译:肾毒性是使用阿霉素(DOX)的限制因素之一。白介素1在DOX诱导的肾毒性中起主要作用,因此我们研究了白介素1受体拮抗剂双醋瑞因(DIA)对DOX诱导的肾毒性的影响。在第11天,通过一次腹膜内注射DOX(15μmg/ kg)诱导的肾毒性的存在或不存在,对大鼠口服DIA(25和50μg/ kg /天),持续15天。我们测量了血清尿素,肌酐,肾脏还原型谷胱甘肽(GSH),丙二醛(MDA),总亚硝酸盐(NOx),过氧化氢酶和超氧化物歧化酶(SOD)的水平。此外,还评估了caspase-3,肿瘤坏死因子α(TNFα),核因子κB(NFκB)的表达以及肾组织病理学。我们的结果表明,两种剂量的DIA均可改善或降低DOX诱导的肾毒性,但双醋瑞因高剂量(DHD)比双醋瑞因低剂量(DLD)表现出更大的改善。与使用DHD的DOX治疗组相比,所有测量参数的显着改善表明了这种保护作用。与DOX处理组相比,DLD显示肌酐,MDA,NOx,GSH,组织病理学和免疫组化参数有显着改善。

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