Zingiber officinale Roscoe alone and in combination with α-tocopherol protect the kidney against cisplatin-induced acute renal failure

Food and Chemical Toxicology

Volumn 45, Issue 6, 2007, Pages 921-927

  Ajith, T A ^a   Nivitha, V ^a   Usha, S ^a  

^a AMALA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Antioxidant; Free radicals; Nephrotoxicity; Zingiber officinale

Indexed keywords

ALCOHOL; ALPHA TOCOPHEROL; CATALASE; CISPLATIN; CREATININE; EVION 400; GINGER EXTRACT; GLUTATHIONE; GLUTATHIONE PEROXIDASE; MALONALDEHYDE; REACTIVE OXYGEN METABOLITE; SCAVENGER; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG; UREA; XENOBIOTIC AGENT;

ACUTE KIDNEY FAILURE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CREATININE BLOOD LEVEL; DOSE RESPONSE; DRUG DOSE COMPARISON; ENZYME ACTIVITY; GINGER; MALE; MOUSE; NEPHROTOXICITY; NONHUMAN; OXIDATIVE STRESS; RENAL PROTECTION; SINGLE DRUG DOSE; UREA BLOOD LEVEL;

ALPHA-TOCOPHEROL; ANIMALS; ANTINEOPLASTIC AGENTS; CATALASE; CISPLATIN; CREATININE; GINGER; GLUTATHIONE; GLUTATHIONE PEROXIDASE; KIDNEY; KIDNEY DISEASES; MALE; MALONDIALDEHYDE; MICE; PLANT EXTRACTS; RHIZOME; SUPEROXIDE DISMUTASE; UREA;

ANIMALIA; MUS; ZINGIBER OFFICINALE;

EID: 33947719629     PISSN: 02786915     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fct.2006.11.014     Document Type: Article

References (38)

1. Ajith T.A., Jose N., and Janardhanan K.K. Amelioration of cisplatin induced nephrotoxicity in mice by ethyl acetate extract of a polypore fungus, Phellinus rimosus. J. Exp. Clin. Cancer. Res. 21 (2002) 487-491
2. Anderson M.E., Naganuma A., and Meister A. Protection against cisplatin toxicity by administration of glutathione ester. FASEB. J. 4 (1990) 3451-4355
3. Arfeen Z., Owen H., Plummer J.L., Ilsley A.H., Sorby-Adams R.A., and Doecke C.J. A double blind randomized controlled trial of ginger for the prevention of postoperative nausea and vomiting. Anaesth. Intensive Care. 23 (1995) 449-452
4. Babu E., Gopalkrishnan V.K., Sriganth N.P., Gopalkrishnan R., and Sakthisekharan D. Cisplatin induced nephrotoxicity and the modulating effect of glutathione ester. Mol. Cell Biochem. 144 (1995) 7-11
5. Beers R.F., and Sizer I.W. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem. 195 (1952) 133-140
6. Boogaard P.J., Lempers E.L., Mulder G.J., and Meerman J.H.N. 4-methylthiobenzoic acid reduces cisplatin nephrotoxicity in rats without compromising anti-tumor activity. Biochem. Pharmacol. 41 (1991) 1997-2003
7. Cetin R., Devrim E., Kilicoglu B., Avei A., Candir O., and Durak I. Cisplatin impairs antioxidant system and causes oxidation in rat kidney tissues: possible protective roles of natural antioxidant foods. J. Appl. Toxicol. 26 (2006) 42-46
8. Conney A.H. Induction of microsomal enzymes by foreign chemicals and carcinogenesis by polycyclic aromatic hydrocarbons: GHA Clowers Memorial Lecture. Cancer Res. 42 (1982) 4875-4917
9. DeWoskin R.S., and Riviere J.E. Cisplatin-induced loss of kidney copper and nephrotoxicity is ameliorated by single dose diethyldithiocarbamate, but not mesna. Toxicol. Appl. Pharmacol. 112 (1992) 182-189
10. Gandara D.R., Perez E.A., Wiebe V., and De Gregorio M.W. Cisplatin chemoprotection and rescue. Pharmacologic modulation of toxicity. Semin. Oncol. 18 (1991) 49-55
11. Grant K.L., and Lutz R.B. Ginger. Am. J. Health Syst. Pharm. 57 (2000) 945-947
12. Hafemann D.G., Sunde R.A., and Houestra W.G. Effect of diatary selenium on erythrocyte and liver glutathione peroxidase in the rat. J. Nutr. 104 (1974) 580-584
13. Halliwell B., and Cross C.E. Oxygen-derived species: Their relation to human disease and environmental stress. Environ. Health Perspect. 102 (1994) 5-12
14. Hamers F.P.T., Gispen W.H., and Neijit J.P. Neurotoxic side effects of cisplatin. Eur. J. Cancer 27 (1991) 372-376
15. Hamers F.P.T., Brakkee J.H., Cavalletti E., and Tedeschi L. Reduced glutathione protects against cisplatin-induced neurotoxicity in rats. Cancer Res. 53 (1993) 544-549
16. Jollow D.J., Mitchell J.R., Zampaglione N., and Gillete J.R. Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacol. 11 (1974) 151-154
17. Kikuzaki H., and Nakatani N. Antioxidant effect of some ginger constituents. J. Food Sci. 58 (1993) 1407-1410
18. Kikuzaki H., Usuguchi J., and Nakatani N. Constituents of zingiberaceae. Diarylheptanoids from the rhizomes of ginger (Zingiber officinale Roscoe). Chem. Pharm. Bull. 39 (1991) 120-122
19. Langner E., Greifenberg S., and Gruenwald J. Ginger: History and use. Adv. Ther. 15 (1998) 25-30
20. Leonetti C., Biroccio A., and Gabellini C. α-Tocopherol protects against cisplatin-induced toxicity without interfering with antitumor efficacy. Int. J. Cancer 104 (2003) 243-250
21. Lowry O.H., Rosebrough N.J., Farr A.L., and Randall R.J. Protein measurement with Folin phenol reagent. J. Biol. Chem. 193 (1951) 265-275
22. Masuda Y., Kikuzaki H., Hisamoto M., and Nakatani N. Antioxidant properties of gingerol related compounds from ginger. Biofactors. 21 (2004) 293-296
23. Mc Cord J.M., and Fridovich I. Superoxide dismutase, an enzymatic function for erythrocuprein. J. Biol. Chem. 244 (1969) 6049-6055
24. Mitchell J.R., Jollow D.J., Potter W.Z., Gillette J.R., and Brodie B.B. Acetaminophen induced hepatic necrosis. Protective role of glutathione. J. Pharmacol. Exp. Ther. 187 (1973) 211-215
25. Moron M.A., Depierre J.W., and Mannervik B. Levels of glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochemica et Biophysica Acta 582 (1979) 67-78
26. Naziroglu M., Karaoglu A., and Aksoy A.O. Selenium and high dose vitamin E administration protects cisplatin-induced oxidative damage to renal and lens tissue in rats. Toxicol. 195 (2004) 221-230
27. Ohkawa H., Ohishi N., and Yagi K. Assay for lipid peroxide in animal tissues by thiobarbituric acid reaction. Annal. Biochem. 95 (1979) 351-358
28. Phillips S., Ruggier R., and Hutchinson S.E. Zingiber officinale (ginger): an antiemetic for day case surgery. Anaesthesia 48 (1993) 715-717
29. Polasa K., and Nirmala K. Ginger: Its role in xenobiotic metabolism. ICMR Bull. 33 (2003) 58-63
30. Rana S.V.S., Allen T., and Singh R. Inevitable glutathione, then and now. Ind. J. Exp. Biol. 40 (2002) 706-716
31. Ravi R.S., Somini S.M., and Rybak L.P. Mechanism of cisplatin ototoxicity. Antioxidant system. Pharmacol. Toxicol. 76 (1995) 386-394
32. Rybak L.P., Ravi P.R., and Somani S.M. Mechanism of protection by diethyldithiocarbamate against cisplatin ototoxicity: antioxidant system. Fund. Appl. Toxicol. 26 (1995) 293-300
33. Sharma R.P. Interactions of cisplatin with cellular zinc and copper in liver and kidney tissues. Pharmacol. Res. Commun. 17 (1985) 197-206
34. Sharma S.S., and Gupta Y.K. Reversal of cisplatin-induced delay in gastric emptying in rats by ginger (Zingiber officinale). J. Ethnopharmacol. 62 (1998) 49-55
35. Simic M.G., and Jovanovic S.V. Free radical mechanism of DNA base damage. In: Simic M.G., Grossman L., and Upton A.G. (Eds). Mechanism of DNA damage and repair (1986), Plenum Press, New York 39-49
36. Vutyavanich T., Kraisarin T., and Ruangsri R. Ginger for nausea and vomiting in pregnancy: randomized, double-masked, placebo-controlled trial. Obstet. Gynecol. 97 (2001) 577-582
37. Walum E. Oral acute toxicity. Environ. Health Perspect. 106 (1998) 497-503
38. Wolfgang G.H.I., Dominic M.A., Walsh K.M., Hoescheli J.D., and Pegg D.G. Comparative nephrotoxicity of a novel platinum compound, cisplatin and carboplatin in male Wistar rats. Toxicol. Sci. 22 (1994) 73-79