Deferoxamine pretreatment prevents Cr(VI)-induced nephrotoxicity and oxidant stress: Role of Cr(VI) chelation

被引:35
作者
Molina-Jijon, Eduardo [1 ]
Zarco-Marquez, Guillermo [1 ,2 ]
Noel Medina-Campos, Omar [1 ]
Lucia Zatarain-Barron, Zyanya [3 ]
Hernandez-Pando, Rogelio [3 ]
Pinzon, Enrique [4 ]
Marina Zavaleta, Rosa [1 ]
Tapia, Edilia [2 ]
Pedraza-Chaverri, Jose [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Chem, Dept Biol, University City 04510, DF, Mexico
[2] Natl Inst Cardiol Ignacio Chavez, Dept Nephrol, Secc 16, Mexico City 14080, DF, Mexico
[3] Natl Inst Med Sci & Nutr Salvador Zubiran, Expt Pathol Sect, Tlalpan 14000, DF, Mexico
[4] Univ Nacl Autonoma Mexico, Anim Care Unit, Fac Med, University City 04510, DF, Mexico
关键词
Nephrotoxicity; Renoprotective; Cr(VI) chelation; Potassium dichromate; Deferoxamine; N-ACETYLCYSTEINE; LIPID-PEROXIDATION; OXIDATIVE STRESS; DESFERRIOXAMINE; CHROMIUM; DAMAGE; CARCINOGENICITY; EFFICACY; FAILURE; IRON;
D O I
10.1016/j.tox.2011.11.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Deferoxamine (DFO) is a recognized iron chelator which has been shown to exert nephroprotection in models of toxic nephropathies. In the present work the potential protective effects of DFO against Cr(VI)-induced nephrotoxicity and oxidant stress were evaluated. Rats were injected with a single injection (15 mg/kg, s.c.) of potassium dichromate (K2Cr2O7). DFO was given as a single i.p. injection 30 min before K2Cr2O7 administration at three different doses (100, 200 and 400 mg/kg). It was found that DFO pretreatment attenuated, in a dose-dependent way, K2Cr2O7-induced renal dysfunction and structural alterations evaluated by serum creatinine, blood urea nitrogen, creatinine clearance, proteinuria, plasma glutathione peroxidase activity, urinary excretion of N-acetyl-beta-D-glucosaminidase and histological analyses. Furthermore. DFO prevented the K2Cr2O7-induced renal oxidant stress and the decrease in the activity of the antioxidant enzymes superoxide dismutase, glutathione reductase, glutathione peroxidase, glutathione-S-transferase and catalase. Finally it was found that DFO, at 400 mg/kg, decreases renal Cr(VI) content which prompted us to evaluate the potential Cr(VI) chelating properties of this compound. Indeed was found in an in vitro assay that DFO was an effective Cr(VI) chelator with an IC50 of 800 mu g. In additional groups of rats was found that DFO posttreatment was ineffective to attenuate K2Cr2O7-induced nephrotoxicity and renal oxidant stress. Furthermore, DFO was unable to modify urinary excretion of total chromium. The nephroprotective effect of DFO against Cr(VI)-induced nephrotoxicity and oxidant stress may be explained, at least partially, by the ability of DFO to chelate Cr(VI) and to attenuate renal Cr(VI) content. However, it cannot be excluded that the ability of DFO to chelate iron may also be involved in the protection observed in our study. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
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