Refaie Marwa M M, Amin Entesar F, El-Tahawy Nashwa F, Abdelrahman Aly M
Department of Pharmacology, Faculty of Medicine, El-Minia University, El-Minia 61111, Egypt.
Department of Histology, Faculty of Medicine, El-Minia University, El-Minia 61111, Egypt.
J Toxicol. 2016;2016:9507563. doi: 10.1155/2016/9507563. Epub 2016 Jan 20.
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 (NO x ), 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, NO x , GSH, histopathology, and immunohistochemical parameters compared to DOX treated group.
肾毒性是使用阿霉素(DOX)的限制因素之一。白细胞介素1在DOX诱导的肾毒性中起主要作用,因此我们研究了白细胞介素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,给大鼠腹腔注射单次剂量的DOX(15mg/kg)诱导或不诱导肾毒性的情况下,口服给予DIA(25和50mg/kg/天),持续15天。我们测量了血清尿素、肌酐、肾还原型谷胱甘肽(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,还评估了半胱天冬酶-3、肿瘤坏死因子α(TNFα)、核因子κB(NFκB)的表达以及肾脏组织病理学。我们的结果表明,两种剂量的DIA均可改善或减轻DOX诱导的肾毒性,但双醋瑞因高剂量(DHD)组的改善效果优于双醋瑞因低剂量(DLD)组。与DOX治疗组相比,使用DHD组在所有测量参数上均有显著改善,这表明了其保护作用。与DOX治疗组相比,DLD组在肌酐、MDA、NOx、GSH、组织病理学和免疫组化参数方面有显著改善。