Effect of N-acetylcysteine on gentamicin-mediated nephropathy in rats

被引:74
|
作者
Mazzon, E
Britti, D
De Sarro, A
Caputi, AP
Cuzzocrea, S
机构
[1] Univ Messina, Sch Med, Inst Pharmacol, I-98100 Messina, Italy
[2] Univ Messina, Dept Vet Med & Pharmacol, Messina, Italy
[3] Univ Messina, Sch Med, Dept Biomorphol, Messina, Italy
关键词
nitric oxide (NO); peroxynitrite; poly(ADP ribose)synthetase; gentamicin; renal injury;
D O I
10.1016/S0014-2999(01)01130-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies were performed on the mechanisms of the protective effects of free-radical scavengers against gentamicin-mediated nephropathy. Administration of gentamicin, 100 mg/kg s.c., for 5 days to rats induced marked renal failure, characterised by a significantly decreased creatinine clearance and increased blood creatinine levels, fractional excretion of sodium Na+, lithium Li+, urine gamma glutamyl transferase and daily urine volume. A significant increase in kidney myeloperoxidase activity and lipid peroxidation was observed in gentamicin-treated rats. Immunohistochemical localisation demonstrated nitrotyrosine formation and poly(ADP-ribose)synthase activation in the proximal tubule from gentamicin-treated rats. Renal histology examination confirmed the tubular necrosis. N-acetylcysteine (10 mg/kg i.p. for 5 days) caused normalisation of the above biochemical parameters. In addition, N-acetylcysteine treatment significantly prevents the gentamicin-induced tubular necrosis. These results suggest that (1) N-acetylcysteine has protective effects on gentamicin-mediated nephropathy, and (2) the mechanisms of the protective effects can be, at least in part, related to interference with peroxynitrite-related pathways. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:75 / 83
页数:9
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