Protection effects of taurine supplementation against cisplatin-induced nephrotoxicity in rats

被引:96
作者
Saad, SY
Al-Rikabi, AC
机构
[1] King Saud Univ, Coll Pharm, Dept Clin Pharm, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Coll Med, Dept Pathol, Riyadh 11451, Saudi Arabia
关键词
taurine; cisplatin; nephrotoxicity; lipid peroxidation;
D O I
10.1159/000048587
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Backgound. Taurine, which is the major intracellular free beta-amino acid, is known to be an antioxidant and a membrane-stabilizing agent. This study was designed to investigate the protective role of taurine supplementation against cisplatin-induced nephrotoxicity. Methods: Male Wistar rats were divided into six groups and treated as follows: (1) saline-treated control drinking tap water, (2) saline-treated plus taurine-supplemented (1.5% taurine in the drinking water), (3) saline-treated plus taurine-depleted (3% P-alanine in the drinking water), (4) cisplatin-treated, CDDP 6 mg/kg intraperitoneally, (5) taurine-supplemented plus CDDP-treated and (6) taurine-depleted plus CDDP-treated. Rats were sacrificed 7 days after CDDP treatment, and serum as well as kidneys were isolated and analyzed. Results: CDDP-treated rats showed increased kidney weight as a percentage of total body weight, serum creatinine and BUN levels and decreased serum albumin and calcium levels. Also, CDDP treatment resulted in a depletion of kidney GSH content, a reduction in the kidney glutathione peroxidase (GSH-Px) activity and increased kidney MDA production level. Taurine supplementation attenuated CDDP-induced nephrotoxicity which was manifested by jeopardizing the elevation in serum creatinine and BUN levels and the reduction in serum albumin and calcium levels. Moreover, taurine supplementation restored kidney GSH content and GSH-Px activity and reduced platinum accumulation and MDA production levels in the kidney tissue following CDDP treatment. Histopathological examination of the kidney of CDDF-treated rats revealed tubular atrophy, tubular necrosis and desquamation of renal tubular cells. However, taurine supplementation protected against CDDP-induced histopathological changes. Conclusions: The data suggest that taurine supplementation effectively attenuates the accumulation of platinum within kidney tissue and counteracts the deleterious effect of CDDP on the renal tubular function. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:42 / 48
页数:7
相关论文
共 37 条
[1]   Hyperlipidaemia in cisplatin-induced nephrotic rats [J].
Abdel-Gayoum, AA ;
El-Jenjan, KB ;
Ghwarsha, KA .
HUMAN & EXPERIMENTAL TOXICOLOGY, 1999, 18 (07) :454-459
[2]  
Antunes LMG, 2000, PHARMACOL RES, V41, P405, DOI 10.1006/phrs.1999.0600
[3]  
Badary OA, 1998, ONCOL RES, V10, P355
[4]   EFFECTS OF CISPLATIN ON URINARY THROMBOXANE B-2 EXCRETION [J].
BLOCHLDAUM, B ;
PEHAMBERGER, H ;
KURZ, C ;
KYRLE, PA ;
WAGNER, O ;
MULLER, M ;
MONITZER, B ;
EICHLER, HG .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 58 (04) :418-424
[5]  
BONSNES RW, 1945, J BIOL CHEM, V158, P581
[6]   The redox pathway of S-nitrosoglutathione, glutathione and nitric oxide in cell to neuron communications [J].
Chiueh, CC ;
Rauhala, P .
FREE RADICAL RESEARCH, 1999, 31 (06) :641-650
[7]   Effects of dietary taurine supplementation or deprivation in aged male Fischer 344 rats [J].
Dawson, R ;
Liu, S ;
Eppler, B ;
Patterson, T .
MECHANISMS OF AGEING AND DEVELOPMENT, 1999, 107 (01) :73-91
[8]  
DOYBAN DC, 1980, J PHARMACOL EXP THER, V213, P551
[9]   TISSUE SULFHYDRYL GROUPS [J].
ELLMAN, GL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) :70-77
[10]   The protective effect of taurine against gentamicin-induced acute tubular necrosis in rats [J].
Erdem, A ;
Gündogan, NÜ ;
Usubütün, A ;
Kilinç, K ;
Erdem, SR ;
Kara, A ;
Bozkurt, A .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2000, 15 (08) :1175-1182