Effect of melatonin, curcumin, quercetin, and resveratrol on acute ferric nitrilotriacetate (Fe-NTA)-induced renal oxidative damage in rats

被引:29
作者
Eybl, V. [1 ]
Kotyzova, D. [1 ]
Cerna, P. [1 ]
Koutensky, J. [1 ]
机构
[1] Charles Univ Prague, Fac Med Pilsen, Dept Pharmacol & Toxicol, Plzen 30166, Czech Republic
关键词
curcumin; ferric nitrilotriacetate; resveratrol; renal oxidative damage; melatonin; quercetin;
D O I
10.1177/0960327108094508
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The influence of melatonin, curcumin, quercetin, and resveratrol pretreatment on ferric nitrilotriacetate (FeNTA)-induced oxidative renal damage was studied. Male Wistar rats were treated orally once daily for 3 days with melatonin (10 mg/kg), curcumin (50 mg/kg), quercetin (15 mg/kg), and resveratrol (10 mg/kg). One hour after the last dose of antioxidants, a single dose of Fe-NTA was administered (8 mg of Fe/kg body weight, i.p.) to pre-treated animals. Twenty-four hours after FeNTA administration, the lipid peroxidation (LP), reduced glutathione (GSH), catalase (CAT), and glutathione peroxidase (GSH-Px) were estimated in kidney homogenates. Iron, zinc, and copper concentrations were estimated in kidney tissue. Administration of Fe-NTA to rats induced renal LP (170%, P < 0.001) and inhibited catalase (78%, P < 0.05) in the kidney. The oral pretreatment with melatonin, curcumin, quercetin, and resveratrol each one was effective in decreasing the Fe-NTA-induced LP (P < 0.001); however, it did not influence the FeNTA-induced inhibition of renal CAT activity. No changes were found in renal GSH level and GSH-Px activity compared to control animals. The pretreatment with antioxidants did not affect the increase in renal iron content, blood urea nitrogen/creatinine ratio, and relative kidney weight of FeNTA-intoxicated rats. The results indicate that the pretreatment with natural antioxidants, curcumin, melatonin, quercetin, and resveratrol, significantly and equally suppressed lipid peroxidation induced by Fe-NTA but had no effect on other markers of FeNTA nephrotoxicity and iron deposition in kidneys.
引用
收藏
页码:347 / 353
页数:7
相关论文
共 49 条
[1]  
Aggarwal BB, 2005, CRC SER MOD NUTR SCI, P349
[2]  
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[3]  
AWAI M, 1979, AM J PATHOL, V95, P663
[4]   HEPATIC LIPID-PEROXIDATION INVIVO IN RATS WITH CHRONIC IRON OVERLOAD [J].
BACON, BR ;
TAVILL, AS ;
BRITTENHAM, GM ;
PARK, CH ;
RECKNAGEL, RO .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (03) :429-439
[5]  
Bahnemann R, 1998, TOXICOL SCI, V46, P166
[6]   Resveratrol, a component of wine and grapes, in the prevention of kidney disease [J].
Bertelli, AAE ;
Migliori, M ;
Panichi, V ;
Origlia, N ;
Filippi, C ;
Das, DK ;
Giovannini, L .
ALCOHOL AND WINE IN HEALTH AND DISEASE, 2002, 957 :230-238
[7]   Protective effect of resveratrol, a polyphenolic phytoalexin on glycerol-induced acute renal failure in rat kidney [J].
Chander, V ;
Chopra, K .
RENAL FAILURE, 2006, 28 (02) :161-169
[8]   Resveratrol, a polyphenolic phytoalexin protects against cyclosporine-induced nephrotoxicity through nitric oxide dependent mechanism [J].
Chander, V ;
Tirkey, N ;
Chopra, K .
TOXICOLOGY, 2005, 210 (01) :55-64
[9]   Nephrotoxicity and its prevention by catechin in ferric nitrilotriacetate promoted oxidative stress in rats [J].
Chopra, K ;
Singh, D ;
Chander, V .
HUMAN & EXPERIMENTAL TOXICOLOGY, 2004, 23 (03) :137-143
[10]   Resveratrol-associated renal toxicity [J].
Crowell, JA ;
Korytko, PJ ;
Morrissey, RL ;
Booth, TD ;
Levine, BS .
TOXICOLOGICAL SCIENCES, 2004, 82 (02) :614-619