Eruca sativa seeds possess antioxidant activity and exert a protective effect on mercuric chloride induced renal toxicity.

Mercuric chloride (HgCl(2)) is a well-known nephrotoxic agent. Increasing number of evidences suggest the role of oxidative stress in HgCl(2) induced nephrotoxicity. Eruca sativa is widely used in folklore medicines and has a good reputation as a remedy of renal ailments. In the present study, the antioxidant potential of ethanolic extract of E. sativa seeds was determined and its protective effect on HgCl(2) induced renal toxicity was investigated. The extract was found to possess a potent antioxidant effect, with a large amount of polyphenols and a high reducing ability. HPLC analysis of the extract revealed glucoerucin and flavonoids to be the major antioxidants present in it. E. sativa extract significantly scavenged several reactive oxygen species (ROS) and reactive nitrogen species (RNS). Feeding of the extract to rats afforded a significant protection against HgCl(2) induced renal toxicity. Subcutaneous administration of 4 mg/kg body weight HgCl(2) induced renal injury evident as a marked elevation in serum creatinine and blood urea nitrogen levels, and histopathological changes such as necrosis, oedema and congestion of stroma and glomeruli. Oxidative modulation of renal tissues following HgCl(2) exposure was evident from a significant elevation in lipid peroxidation and attenuation in glutathione (GSH) contents and activities of antioxidant enzymes viz., catalase (CAT), glutathione peroxidase (GPX), superoxide dismutase (SOD) and glutathione reductase (GR). Oral administration of E. sativa extract to rats at a dose regimen: 50-200 mg/kg body weight for 7 days prior to HgCl(2) treatment significantly and dose dependently protected against alterations in all these diagnostic parameters. The data obtained in the present study suggests E. sativa seeds to possess a potent antioxidant and renal protective activity and preclude oxidative damage inflicted to the kidney.

[1]  M. Athar,et al.  Potassium bromate (KBrO3) induces renal proliferative response and damage by elaborating oxidative stress. , 1999, Cancer letters.

[2]  G. Duggin,et al.  Differential distribution of glutathione and glutathione-related enzymes in rabbit kidney. Possible implications in analgesic nephropathy. , 1984, Biochemical pharmacology.

[3]  G. Şener,et al.  Melatonin protects against mercury(II)-induced oxidative tissue damage in rats. , 2003, Pharmacology & toxicology.

[4]  J. S. Woods,et al.  Studies on Hg(II)-induced H2O2 formation and oxidative stress in vivo and in vitro in rat kidney mitochondria. , 1993, Biochemical pharmacology.

[5]  H. Kappus,et al.  Cellular toxicity and lipid peroxidation in response to mercury. , 1982, Toxicology and applied pharmacology.

[6]  N. Hogg Free Radicals in Disease , 1998, Seminars in reproductive endocrinology.

[7]  T. Dinis,et al.  Action of phenolic derivatives (acetaminophen, salicylate, and 5-aminosalicylate) as inhibitors of membrane lipid peroxidation and as peroxyl radical scavengers. , 1994, Archives of biochemistry and biophysics.

[8]  O. Wada,et al.  Inducible nitric oxide synthase expression in mercury chloride-induced acute tubular necrosis. , 1998, Industrial health.

[9]  G. Duggin,et al.  Low activities of glutathione-related enzymes as factors in the genesis of urinary bladder cancer. , 1984, Cancer research.

[10]  P. Poronnik,et al.  Role of oxidative stress in age-associated chronic kidney pathologies. , 2005, Advances in chronic kidney disease.

[11]  L. M. Perry,et al.  Medicinal Plants of East and Southeast Asia: Attributed Properties and Uses , 1980 .

[12]  I. Fridovich,et al.  Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. , 1971, Analytical biochemistry.

[13]  M. Athar,et al.  Glyceryl trinitrate, a nitric oxide donor, abrogates ferric nitrilotriacetate-induced oxidative stress and renal damage. , 2003, Archives of biochemistry and biophysics.

[14]  J. Pedraza-Chaverri,et al.  Protective effect of diallyl sulfide on oxidative stress and nephrotoxicity induced by gentamicin in rats , 2003, Molecular and Cellular Biochemistry.

[15]  J. Sedlák,et al.  Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. , 1968, Analytical biochemistry.

[16]  T. Behrens,et al.  Renal oxidant injury and oxidant response induced by mercury. , 1996, Kidney international.

[17]  J. Klaunig,et al.  Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea. , 1989, Carcinogenesis.

[18]  J. Fahey,et al.  Antioxidant functions of sulforaphane: a potent inducer of Phase II detoxication enzymes. , 1999, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[19]  T. H. Lin,et al.  Lipid peroxidation in rats administrated with mercuric chloride , 1996, Biological Trace Element Research.

[20]  O. Aruoma,et al.  Action of hypochlorous acid on the antioxidant protective enzymes superoxide dismutase, catalase and glutathione peroxidase. , 1987, The Biochemical journal.

[21]  M. Athar,et al.  Attenuation of iron-nitrilotriacetate (Fe-NTA)-mediated renal oxidative stress, toxicity and hyperproliferative response by the prophylactic treatment of rats with garlic oil. , 1998, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[22]  N. Vaziri Roles of oxidative stress and antioxidant therapy in chronic kidney disease and hypertension , 2004, Current opinion in nephrology and hypertension.

[23]  M. Athar,et al.  Ferric nitrilotriacetate promotes N-diethylnitrosamine-induced renal tumorigenesis in the rat: implications for the involvement of oxidative stress. , 1998, Carcinogenesis.

[24]  M. Oyaizu Studies on products of browning reaction--antioxidative activities of products of browning reaction prepared from glucosamine , 1986 .

[25]  D. Miller,et al.  Mercury-induced H2O2 production and lipid peroxidation in vitro in rat kidney mitochondria. , 1991, Biochemical pharmacology.

[26]  M. Paller Free radical scavengers in mercuric chloride-induced acute renal failure in the rat. , 1985, The Journal of laboratory and clinical medicine.

[27]  Z. Yaniv,et al.  Tradition, uses and Biodiversity of rocket (Eruca Sativa, Brassicaceae) in Israel , 1998, Economic Botany.

[28]  M. D. de Broe,et al.  Time course of growth factor expression in mercuric chloride acute renal failure. , 1995, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[29]  R. Hare,et al.  Endogenous Creatinine in Serum and Urine.∗ † , 1950, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[30]  M. Nava,et al.  Melatonin attenuates acute renal failure and oxidative stress induced by mercuric chloride in rats. , 2000, American journal of physiology. Renal physiology.

[31]  K. Javed,et al.  Effect of Rheum emodi (Revand Hindi) on renal functions in rats. , 2005, Journal of ethnopharmacology.

[32]  C. Cho,et al.  A major inducer of anticarcinogenic protective enzymes from broccoli: isolation and elucidation of structure. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[33]  J. S. Woods,et al.  Stimulation of porphyrinogen oxidation by mercuric ion. II. Promotion of oxidation from the interaction of mercuric ion, glutathione, and mitochondria-generated hydrogen peroxide. , 1990, Molecular pharmacology.

[34]  J. Fahey,et al.  Comprehensive chromatographic and spectroscopic methods for the separation and identification of intact glucosinolates. , 1996, Analytical biochemistry.

[35]  P. R. Miles,et al.  Cytosolic factors which affect microsomal lipid peroxidation in lung and liver. , 1981, Archives of biochemistry and biophysics.

[36]  B. Halliwell,et al.  Nitric oxide and peroxynitrite. The ugly, the uglier and the not so good: a personal view of recent controversies. , 1999, Free radical research.

[37]  Rudolfs K. Zalups,et al.  Molecular interactions with mercury in the kidney. , 2000, Pharmacological reviews.

[38]  Gow-Chin Yen,et al.  Antioxidant activity of various tea extracts in relation to their antimutagenicity , 1995 .

[39]  P. Kroon,et al.  Ontogenic profiling of glucosinolates, flavonoids, and other secondary metabolites in Eruca sativa (salad rocket), Diplotaxis erucoides (wall rocket), Diplotaxis tenuifolia (wild rocket), and Bunias orientalis (Turkish rocket). , 2006, Journal of agricultural and food chemistry.

[40]  W. Pfaller,et al.  Glutathione depletion and in vitro lipid peroxidation in mercury or maleate induced acute renal failure. , 1983, Biochemical pharmacology.

[41]  L. Valgimigli,et al.  Direct antioxidant activity of purified glucoerucin, the dietary secondary metabolite contained in rocket (Eruca sativa Mill.) seeds and sprouts. , 2005, Journal of agricultural and food chemistry.

[42]  M. Athar,et al.  Nordihydroguairetic acid is a potent inhibitor of ferric-nitrilotriacetate-mediated hepatic and renal toxicity, and renal tumour promotion, in mice. , 1999, Carcinogenesis.

[43]  M. Silvia Taga,et al.  Chia seeds as a source of natural lipid antioxidants , 1984 .

[44]  Chang-Beohm Ahn,et al.  Effects of Juglans sinensis Dode extract and antioxidant on mercury chloride-induced acute renal failure in rabbits. , 2002, Journal of Ethnopharmacology.

[45]  J. C. Uphof Dictionary of Economic Plants , 1968 .

[46]  D. Jollow,et al.  Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. , 1974, Pharmacology.

[47]  S. Aslam,et al.  Nitric oxide, oxidative stress, and progression of chronic renal failure. , 2004, Seminars in nephrology.