Efficacy of some antioxidants supplementation in reducing oxidative stress post sodium tungstate exposure in male wistar rats

Journal of Trace Elements in Medicine and Biology

Volumn 28, Issue 2, 2014, Pages 233-239

  Sachdeva, S ^a   Flora, S J S ^a  

^a DEFENCE RESEARCH AND DEVELOPMENT ESTABLISHMENT   (India)

Author keywords

Antioxidant; Flavonoids; Oxidative stress; Rats; Sodium tungstate toxicity

Indexed keywords

ACETYLCYSTEINE; ANTIOXIDANT; CATALASE; GLUTATHIONE; GLUTATHIONE DISULFIDE; NARINGENIN; PORPHOBILINOGEN SYNTHASE; QUERCETIN; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; THIOCTIC ACID; TUNGSTATE SODIUM; TUNGSTEN; UNCLASSIFIED DRUG; INORGANIC COMPOUND; SODIUM TUNGSTATE; THIOBARBITURIC ACID REACTIVE SPECIES; SODIUM TUNGSTATE(VI); TUNGSTEN DERIVATIVE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG EFFICACY; DRUG MECHANISM; ENVIRONMENTAL EXPOSURE; ENZYME INHIBITION; LIVER LEVEL; LIVER PROTECTION; LIVER TOXICITY; MALE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT; SUPPLEMENTATION; WEIGHT REDUCTION; DIET SUPPLEMENTATION; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; HEAVY METAL POISONING; SIGNAL TRANSDUCTION; SODIUM TUNGSTATE TOXICITY; ANIMAL; BLOOD; BODY WEIGHT; DRUG EFFECTS; LIVER; PATHOLOGY; SPLEEN; TOXICITY; WISTAR RAT;

ANIMALIA; RATTUS; RATTUS NORVEGICUS;

ANIMALS; ANTIOXIDANTS; BODY WEIGHT; DIETARY SUPPLEMENTS; LIVER; MALE; OXIDATIVE STRESS; PORPHOBILINOGEN SYNTHASE; RATS, WISTAR; SPLEEN; TUNGSTEN COMPOUNDS;

EID: 84898044840     PISSN: 0946672X     EISSN: 18783252     Source Type: Journal    
DOI: 10.1016/j.jtemb.2014.01.004     Document Type: Article

References (47)

1. Kerley C.L., Easterly C.E., Eckerman K.F., Jones T.D., Legett R.W., Munro N.B. Environmental acceptability of high-performance alternatives for depleted uranium penetrators 1996, U.S. Dept of Energy, DE 97051265.
2. Koutsospyros A., Braida W., Christodoulatos C., Dermatas D., Strigul N. A review of tungsten. From environmental obscurity to scrutiny. J Hazard Mater 2006, 136:1-19.
3. Johnson D.R., Ang C., Bednar A.J., Inouye L.S. Tungsten effects on phosphate-dependent biochemical pathways are species and liver cell line dependent. Toxicol Sci 2010, 116(2):523-532.
4. Lagarde F., Leroy M. Metabolism and toxicity of tungsten in humans and animals. Met Ions Biol Syst 2002, 39:741-759.
5. Le Lamer S., Poucheret P., Cros G., de Richter R.K., Bonnet P.A., Bressolle F. Pharmacokinetics of sodium tungstate in rat and dog: a population approach. J Pharmacol Exp Ther 2000, 294(2):714-721.
6. Nakhaee A., Bokaeian M., Akbarzadeh A., Hashemi M. Sodium tungstate attenuate oxidative stress in brain tissue of streptozotocin-induced diabetic rats. Biol Trace Elem Res 2010, 136(2):221-231.
7. Zafra D., Nocito L., Domínguez J., Guinovart J.J. Sodium tungstate activates glycogen synthesis through a non-canonical mechanism involving G-proteins. FEBS Lett 2013, 587(3):291-296.
8. Sachdeva S., Kushwaha P., Flora S.J. Effects of sodium tungstate on oxidative stress enzymes in rats. Toxicol Mech Methods 2013, 23(7):519-527.
9. Guandalini G.S., Zhang L., Fornero E., Centeno J.A., Mokashi V.P., Ortiz P.A., et al. Tissue distribution of tungsten in mice following oral exposure to sodium tungstate. Chem Res Toxicol 2011, 24(4):488-493.
10. Flora S.J.S., Shrivastava R., Mittal M. Chemistry and pharmacological properties of some natural and synthetic antioxidants for heavy metal toxicity. Current Med Chem 2013, 20(36):4540-4574.
11. Flora S.J. Structural, chemical and biological aspects of antioxidants for strategies against metal and metalloid exposure. Oxid Med Cell Longev 2009, 2(4):191-206.
12. Yamamoto H., Watanabe T., Mizuno H., Endo K., Fukushige J., Hosokawa T., et al. The antioxidant effect of DL-alpha-lipoic acid on copper-induced acute hepatitis in Long-Evans Cinnamon (LEC) rats. Free Radic Res 2001, 34(1):69-80.
13. Gurer H., Ozgunes H., Oztezcan S., Ercal N. Antioxidant role of alpha-lipoic acid in lead toxicity. Free Radic Biol Med 1999, 27(1, 2):75-81.
14. Samuel S., Subathra M., Devi M.A., Panneerselvam C. Arsenic intoxication induced reduction of glutathione level and of the activity of related enzymes in rat brain regions: reversal by lipoic acid. Arch Toxicol 2005, 79:140-146.
15. Pande M., Flora S.J. Lead induced oxidative damage and its response to combined administration of alpha-lipoic acid and succimers in rats. Toxicology 2002, 15(177(2-3)):187-196.
16. Pande M., Mehta A., Pant B.P., Flora S.J. Combined administration of a chelating agent and an antioxidant in the prevention and treatment of acute lead intoxication in rats. Environ Toxicol Pharmacol 2001, 9(4):173-184.
17. Flora S.J.S., Pachauri V. Chelation in Metal Intoxication. Int J Environ Res Public Health 2010, 7(7):2745-2788.
18. Mishra D., Flora S.J. Quercetin administration during chelation therapy protects arsenic induced oxidative stress in mice. Biol Trace Elem Res 2008, 122(2):137-147.
19. Kanno S., Tomizawa A., Hiura T., Osanai Y., Shouji A., Ujibe M., et al. Inhibitory effects of naringenin on tumor growth in human cancer cell lines and sarcoma S-80-implanted mice. Biol Pharm Bull 2005, 28(3):527-530.
20. Hirai S., Kim Y.I., Goto T., Kang M.S., Yoshimura M., Obata A., et al. Inhibitory effect of naringenin chalcone on inflammatory changes in the interaction between adipocytes and macrophages. Life Sci 2007, 81(16):1272-1279.
21. Lee M.H., Yoon S., Moon J.O. The flavonoid naringenin inhibits dimethylnitrosamine induced liver damage in rats. Biol Pharm Bull 2004, 27:72-76.
22. Jain A., Yadav A., Bozhkov A.I., Padalko V.I., Flora S.J. Therapeutic efficacy of silymarin and naringenin in reducing arsenic-induced hepatic damage in young rats. Ecotoxicol Environ Saf 2011, 74(4):607-614.
23. Cohen H.J., Drew R.T., Johnson J.L., Rajagopalan K.V. Molecular basis of the biological function of molybdenum: the relationship between sulfite oxidase and the acute toxicity of bisulfite and SO2. Proc Natl Acad Sci USA 1973, 70(12):3655-3659.
24. Caylak E., Aytekin M., Halifeoglu I. Antioxidant effects of methionine, α-lipoic acid, Nacetylcysteine and homocysteine on lead-induced oxidative stress to erythrocytes in rats. Exp Toxicol Pathol 2008, 60(4-5):289-294.
25. Dwivedi N., Flora S.J.S. (2011). Dose dependent efficacy of quercetin in preventing arsenic induced oxidative stress in rat blood and liver. J Cell Tissue Res 2011, 11(1):2605-2611.
26. Steck T.L., Kant J.A. Preparation of impermeable ghosts and inside-out vesicles from human erythrocyte membranes. Method Enzymol 1974, 31:172-180.
27. Berlin A., Schaller K.H. European standardized method for the determination of delta aminolevulinic dehydratase in blood. Z. Klin. Chem. Klin. Biochem. 1974, 12:389-390.
28. Socci D.J., Bjugstad K.B., Jones H.C., Pattisapu J.V., Arendash G.W. Evidence that oxidative stress is associated with the pathophysiology of inherited hydrocephalus in the H-Tx rat model. Exp Neurol 1999, 155:109-117.
29. Ellman G.L. Tissue sulfhydryl groups. Arch Biochem 1959, 82:70-77.
30. Jollow D.J., Mitchell J.R., Zamppaglione Z., Gillette J.R. Bromobenzene induced liver necrosis. Protective role of glutathione and evidence for 3,4 -bromobenzene oxide as the hepatotoxic metabolites. Pharmacology 1974, 11:151.
31. Stocks J., Dormandy T.L. The autoxidation of human red cell lipids induced by hydrogen peroxide. Br J Haematol 1971, 20(1):95-111.
32. Ohkawa H., Onishi N., Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979, 95:351-358.
33. Hissin P.J., Hilf R. A fluorometric method for determination of oxidized and reduced glutathione in tissues. Anal Biochem 1974, 74:214-226.
34. Kakkar P., Das B., Viswanathan P.N. A modified spectrophotometric assay of superoxide dismutase. Ind J Biochem Biophys 1984, 21:130-132.
35. Sinha A.K. Colorimetric assay of catalase. Anal Biochem 1972, 47:389-394.
36. Strigul N. Does speciation matter for tungsten ecotoxicology?. Ecotoxicol Environ Saf 2010, 73(6):1099-1113.
37. Ferrali M., Signorini C., Ciccoli L., Bambagioni S., Rossi V., Pompella A., Comporti M. Protection of erythrocytes against oxidative damage and autologous immunoglobulin G (IgG) binding by iron chelator fluor-benzoil-pyridoxal hydrazone. Biochem Pharmacol 2000, 59(11):1365-1373.
38. Flora S.J., Chouhan S., Kannan G.M., Mittal M., Swarnkar H. Combined administration of taurine and monoisoamyl DMSA protects arsenic induced oxidative injury in rats. Oxid Med Cell Longev 2008, 1(1):39-45.
39. Flora S.J., Bhadauria S., Kannan G.M., Singh N. Arsenic induced oxidative stress and the role of antioxidant supplementation during chelation: a review. J Environ Biol 2007, 2:333-347.
40. Corpas I., Benito M.J., Marquina D., Castillo M., Lopez N., Antonio M.T. Gestational and lactational lead intoxication produces alterations in the hepatic system of rat pups. Ecotoxicol Environ Saf 2002, 51(1):35-43.
41. De Flora S., Cesarone C.F., Balansky R.M., Albini A., D'Agostini F., Bennicelli C. Chemo preventive properties and mechanisms of N-Acetylcysteine. The experimental background. J Cell Biochem 1995, 22:33-41.
42. Balcerzak M., Kopacz M., Kosiorek A., Swiecicka E., Kus S. Spectrophotometric studies of the interaction of noble metals with quercetin and quercetin-5'-sulfonic acid. Anal Sci 2004, 20(9):1333-1337.
43. Gurer H., Ercal N. Can antioxidants be beneficial in the treatment of lead poisoning?. Free Radic Biol Med 2000, 29(10):927-945.
44. Meyer A.J., Hell R. Glutathione homeostasis and redox-regulation by sulfhydryl groups. Photosynth Res 2005, 86(3):435-457.
45. Pastore A., Federici G., Bertini E., et al. Analysis of glutathione implication in redox and detoxification. Clin Chim Acta 2003, 333(1):19-39.
46. Schafer F.Q., Buettner G.R. Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Radic Biol Med 2001, 30(11):1191-1212.
47. Bors W., Heller W., Michel C., Saran M. Radical chemistry of flavonoid antioxidants. Adv Exp Med Biol 1990, 264:165-170.