Expression of hepatic antioxidant genes in l-thyroxine-induced hyperthyroid rats: Regulation by vitamin E and curcumin

Chemico-Biological Interactions

Volumn 183, Issue 2, 2010, Pages 304-316

  Subudhi, Umakanta ^a   Chainy, Gagan B N ^a  

^a UTKAL UNIVERSITY   (India)

Author keywords

Antioxidant gene expression; Curcumin; Rat liver; Thyroid hormone; Vitamin E

Indexed keywords

ALPHA TOCOPHEROL; CATALASE; COPPER ZINC SUPEROXIDE DISMUTASE; CURCUMIN; GLUTATHIONE PEROXIDASE 1; GLUTATHIONE REDUCTASE; LEVOTHYROXINE; LIVER ENZYME; MANGANESE SUPEROXIDE DISMUTASE; MESSENGER RNA; MITOCHONDRIAL ENZYME; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; CYTOSOL; DRUG EFFECT; DRUG MECHANISM; ENZYME ACTIVITY; ENZYME INHIBITION; GENE EXPRESSION REGULATION; HYPERTHYROIDISM; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATIVE STRESS; RAT;

ANIMALS; ANTIOXIDANTS; CATALASE; CURCUMIN; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; HYPERTHYROIDISM; LIVER; MALE; OXIDATIVE STRESS; OXIDOREDUCTASES; RATS; SUPEROXIDE DISMUTASE; THYROXINE; VITAMIN E;

RATTUS;

EID: 72149116692     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2009.11.004     Document Type: Article

References (63)

1. Yen P.M. Physiological and molecular basis of thyroid hormone action. Physiol. Rev. 81 (2001) 1097-1142
2. Gulcelik M.A., Gulcelik N.E., Dinc S., Kuru B., Camlibel M., and Alagol H. The incidence of hyperthyroidism in patients with thyroid cancer in an area of iodine deficiency. J. Surg. Oncol. 94 (2006) 35-39
3. Das K., and Chainy G.B.N. Modulation of rat liver antioxidant defence system by thyroid hormone. Biochim. Biophys. Acta 1537 (2001) 1-13
4. Chattopadhyay S., Sahoo D.K., Subudhi U., and Chainy G.B.N. Differential expression profiles of antioxidant enzymes and glutathione redox status in hyperthyroid rats: a temporal analysis. Comp. Biochem. Physiol. C 146 (2007) 383-391
5. Subudhi U., Das K., Paital B., Bhanja S., and Chainy G.B.N. Alleviation of enhanced oxidative stress and oxygen consumption of l-thyroxine induced hyperthyroid rat liver mitochondria by vitamin E and curcumin. Chem. Biol. Interact. 173 (2008) 105-114
6. Majima T., Komatsu Y., Doi K., Takagi C., Shigemoto M., Fukao A., Morimoto T., Corners J., and Nakao K. Clinical significance of risedronate for osteoporesis in the initial treatment of male patients with Graves' disease. J. Bone Miner. Metab. 24 (2006) 105-113
7. Roffi M., Cattaneo F., and Brandle M. Thyrotoxicosis and the cardiovascular system. Miner. Endocrinol. 30 (2005) 47-58
8. Fadel B.M., Ellahham S., Ringel M.D., Lindsay Jr. J., Wartofsky L., and Burman K.D. Hyperthyroid heart disease. Clin. Cardiol. 23 (2000) 402-408
9. Venditti P., and Di Meo S. Thyroid hormone-induced oxidative stress. Cell. Mol. Life Sci. 63 (2006) 414-434
10. Pereira B., Rosa L.F., Safi D.A., Bechara E.J., and Curi R. Control of superoxide dismutase, CAT and glutathione peroxidase activities in rat lymphoid organs by thyroid hormones. J. Endocrinol. 140 (1994) 73-77
11. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine. 3rd ed. (2001), Oxford University Press, New York
12. Kehrer J.P. Free radicals as mediators of tissue injury and disease. Crit. Rev. Toxicol. 23 (1993) 21-48
13. Videla L.A. Energy metabolism, thyroid calorigenesis, and oxidative stress: functional and cytotoxic consequences. Redox Report 5 (2000) 265-275
14. Huang Y., He T., and Domann F.E. Decreased expression of manganese superoxide dismutase in transformed cells is associated with increased cytosine methylation of the SOD2 gene. DNA Cell Biol. 18 (1999) 643-652
15. Sato K., Ito K., Kohara H., Yamaguchi Y., Adachi K., and Endo H. Negative regulation of catalase gene expression in hepatoma cells. Mol. Cell. Biol. 12 (1992) 2525-2533
16. Skrzycki M., Scibior D., Podsiad M., and Czeczot H. Activity and protein level of CuZn SOD and Mn SOD in benign and malignant liver tumors. Clin. Biochem. 41 (2008) 91-96
17. Mates J.M., Perez-Gomez C., and Nunez de Castro I. Antioxidant enzymes and human diseases. Clin. Biochem. 32 (1999) 595-603
18. Verma I.M., and Somia N. Gene therapy: promises, problems and prospects. Nature 389 (1997) 239-242
19. Aggarwal B.B., and Harikumar K.B. Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases. Int. J. Biochem. Cell Biol. 41 (2009) 40-59
20. Zingg J.M. Vitamin E: an overview of major research directions. Mol. Aspects Med. 28 (2007) 400-422
21. Subudhi U., Das K., Paital B., Bhanja S., and Chainy G.B.N. Supplementation of curcumin and vitamin E enhances oxidative stress, but restores hepatic histoarchitecture in hypothyroid rats. Life Sci. 84 (2009) 372-379
22. Hatcher H., Planalp R., Cho J., Torti F.M., and Torti S.V. Curcumin: from ancient medicine to current clinical trials. Cell. Mol. Life Sci. 65 (2008) 1631-1652
23. Das K., Samanta L., and Chainy G.B.N. A modified spectrophotometric assay of superoxide dismutase using nitrite formation of superoxide radicals. Indian J. Biochem. Biophys. 37 (2000) 201-204
24. Okado-Matsumoto A., and Fridovich I. Subcellular distribution of superoxide dismutase (SOD) in rat liver: CuZn-SOD in mitochondria. J. Biol. Chem. 276 (2001) 38388-38393
25. Inarrea P., Moini H., Rettori D., Han D., Martinez J., Garcia I., Fernandez-Vizarra E., Iturralde M., and Cadenas E. Redox activation of mitochondrial intermembrane space Cu Zn-superoxide dismutase. Biochem. J. 387 (2005) 203-209
26. Cohen G., Dembiec D., and Marcus J. Measurement of catalase activity in tissue extracts. Anal. Biochem. 34 (1970) 30-38
27. Carmagnol F., Sinet P.M., and Jerome H. Selenium-dependent and non-selenium-dependent glutathione peroxidases in human tissue extracts. Biochim. Biophys. Acta 759 (1983) 49-57
28. Massey V., and Williams C.H. On the reaction mechanism of yeast glutathione reductase. J. Biol. Chem. 240 (1965) 4470-4481
29. Griffith O.W. Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal. Biochem. 106 (1980) 207-212
30. Olsvik P.A., Kristensen T., Waagbo R., Rosseland B.O., Tollefsen K.E., Baeverfjord G., and Berntssen M.H.G. mRNA expression of antioxidant enzymes (SOD, CAT and GSH-Px) and lipid peroxidative stress in liver of Atlantic salmon (Salmo salar) exposed to hyperoxic water during smoltification. Comp. Biochem. Physiol. C 141 (2005) 314-323
31. Sen C.K., and Packer L. Antioxidant and redox regulation of gene transcription. FASEB J. 10 (1996) 709-720
32. Mayo J.C., Sainz R.M., Antoli I., Herrera F., Martin V., and Rodriguez C. Melatonin regulation of antioxidant enzyme gene expression. Cell. Mol. Life Sci. 59 (2002) 1706-1713
33. Guidot D.M., Rapine J.E., Kitlowski A.D., Flores S.C., Nelson S.K., Wright R.M., and McCord J.M. Mitochondrial respiration scavenges extramitochondrial superoxide anion via a nonenzymatic mechanism. J. Clin. Invest. 96 (1995) 1131-1136
34. Erdamar H., Demirci H., Yaman H., Erbil M.K., Yakar T., Sancak B., Elbeg S., Biberoglu G., and Yetkin I. The effect of hypothyroidism, hyperthyroidism and their treatment on parameters of oxidative stress and antioxidant status. Clin. Chem. Lab. Med. 46 (2008) 1004-1010
35. Fernandez V., Tapia G., Varela P., Castillo I., Mora C., Moya F., Orellana M., and Videla L.A. Redox up-regulated expression of rat liver manganese superoxide dismutase and Bcl-2 by thyroid hormone is associated with inhibitor of κB-α phosphorylation and nuclear factor-κB activation. J. Endocrinol. 186 (2005) 539-547
36. Chung D.J., Wright A.E., and Clerch L.B. The 3′ untranslated region of manganese superoxide dismutase RNA contains a translational enhancer element. Biochemistry 37 (1998) 16298-16306
37. Santiard D. Inactivation of Cu, Zn-superoxide dismutase by free radicals derived from ethanol metabolism: a gamma radiolysis study. Free Radic. Biol. Med. 19 (1995) 121-127
38. Abe J., and Berk B.C. Fyn and JAK2 mediate Ras activation by reactive oxygen species. J. Biol. Chem. 274 (1999) 21003-21010
39. Valko M., Rhodes C.J., Moncol J., Izakovic M., and Mazur M. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem. Biol. Interact. 160 (2006) 1-40
40. Fernandez V., Tapia G., Varela P., Romanque P., Cartier-Ugarte D., and Videla L.A. Thyroid hormone-induced oxidative stress in rodents and humans: a comparative view and relation to redox regulation of gene expression. Comp. Biochem. Physiol. C 142 (2006) 231-239
41. Ho Y., Xiong Y., Ma W., Spector A., and Ho D.S. Mice lacking catalase develop normally but show differential sensitivity to oxidant tissue injury. J. Biol. Chem. 279 (2004) 32804-32812
42. Remmen H.V., Williams M.D., Yang H., Walter C.A., and Richardson A. Analysis of the transcriptional activity of the 5′-flanking region of the rat catalase gene in transiently transfected cells and in transgenic mice. J. Cell Physiol. 174 (1998) 18-26
43. Allen R.G., and Tresini M. Oxidative stress and gene regulation. Free Radic. Biol. Med. 28 (2000) 463-499
44. Cao C., Leng Y., and Kufe D. Catalase activity is regulated by c-Abl and Arg in the oxidative stress response. J. Biol. Chem. 278 (2003) 29667-29675
45. Cao C., Leng Y., Liu X., Yi Y., Li P., and Kufe D. Catalase is regulated by ubiquitination and proteosomal degradation. Role of the c-Abl and Arg tyrosine kinases. Biochemistry 42 (2003) 10348-10353
46. Cao C., Leng Y., and Kufe D. Functional interaction between the c-Abl and Arg protein tyrosine kinases in the oxidative stress response. J. Biol. Chem. 278 (2003) 12961-12967
47. Sadi G., Yilmaz O., and Guray T. Effect of vitamin C and lipoic acid on streptozotocin-induced diabetes gene expression: mRNA and protein expressions of Cu/Zn-SOD and catalase. Mol. Cell. Biochem. 309 (2008) 109-116
48. Banudevi S., Krishnamoorthy G., Venkataraman P., Vignesh C., Aruldhas M.M., and Arunakaran J. Role of α-tocopherol on antioxidant status in liver, lung and kidney on PCB exposed male albino rats. Food Chem. Toxicol. 44 (2006) 2040-2046
49. Kalpana C., Sudheer A.R., Rajasekharan K.N., and Menon V.P. Comparative effects of curcumin and its synthetic analogue on tissue lipid peroxidation and antioxidant status during nicotine-induced toxicity. Singapore Med. J. 48 (2007) 124-130
50. de Haan J.B., Bladier C., Griffiths P., Kelner M., O'Shea R.D., Cheung N.S., Bronson R.T., Silvestro M.J., Wild S., Zheng S.S., Beart P.M., Hertzog P.J., and Kola I. Mice with a homozygous null mutation for the most abundant glutathione peroxidase, GPx1 show increased susceptibility to the oxidative stress-inducing agents paraquat and hydrogen peroxide. J. Biol. Chem. 273 (1998) 22528-22536
51. Esposito L.A., Kokoszka J.E., Waymire K.G., Cottrell B., MacGregor G.R., and Wallace D.C. Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene. Free Radic. Biol. Med. 28 (2000) 754-766
52. Seymen H.O., Seven A., Civelek S., Yigit G., Hatemi H., and Burcak G. Evaluation of antioxidant status in liver tissues: effect of iron supplementation in experimental hyperthyroidism. J. Basic Clin. Physiol. Pharmacol. 10 (1999) 315-325
53. Morini P., Casalino E., Sblanco C., and Landriscina C. The response of rat liver lipid peroxidation, antioxidant enzyme activities and glutathione concentration to the thyroid hormone. Int. J. Biochem. 23 (1991) 1025-1030
54. Venditti P., Balestrieri M., Di Meo S., and De Leo T. Effect of thyroid state on lipid peroxidation, antioxidant defences, and susceptibility to oxidative stress in rat tissues. J. Endocrinol. 155 (1997) 151-157
55. Vibet S., Goupille C., Bougnoux P., Steghens J.P., Gore J., and Maheo K. Sensitization by docosahexaenoic acid (DHA) of breast cancer cells to anthracyclines through loss of glutathione peroxidase (GPx1) response. Free Radic. Biol. Med. 44 (2008) 1483-1491
56. Bains J.S., and Shaw C.A. Neurodegenerative disorders in humans: the role of glutathione in oxidative stress-mediated neuronal death. Brain Res. Rev. 25 (1997) 335-358
57. Fernandez V., and Videla L.A. Hepatic glutathione biosynthetic capacity in hyperthyroid rats. Toxicol. Lett. 89 (1996) 85-89
58. Sahoo D.K., Roy A., and Chainy G.B.N. Protective effects of vitamin E and curcumin on l-thyroxine-induced rat testicular oxidative stress. Chem. Biol. Interact. 176 (2008) 121-128
59. Vulpe C.D., and Packman S. Cellular copper transport. Annu. Rev. Nutr. 15 (1995) 293-322
60. Limon-Pacheco J.H., Hernandez N.A., Fanjul-Moles M.L., and Gonsebatt M.E. Glutathione depletion activates mitogen-activated protein kinase (MAPK) pathways that display organ-specific responses and brain protection in mice. Free Radic. Biol. Med. 43 (2007) 1335-1347
61. Kosower N.S., and Kosower E.M. The glutathione status of cells. Int. Rev. Cytol. 54 (1978) 109-160
62. Miyamoto Y., Koh Y.H., Park Y.S., Fujiwara N., Sakiyama H., Misonou Y., Ookawara T., Suzuki K., Honke K., and Taniguchi N. Oxidative stress caused by inactivation of glutathione peroxidase and adaptive responses. Biol. Chem. 384 (2003) 567-574
63. Pigeolet E., and Remacle J. Susceptibility of glutathione peroxidase to proteolysis after oxidative alteration by peroxides and hydroxyl radicals. Free Radic. Biol. Med. 11 (1991) 191-195