Thioacetamide-induced cirrhosis in selenium-adequate mice displays rapid and persistent abnormity of hepatic selenoenzymes which are mute to selenium supplementation

Toxicology and Applied Pharmacology

Volumn 224, Issue 1, 2007, Pages 81-88

  Jinsong Zhang, ^a   Huali Wang, ^a   Hanqing Yu, ^a  

^a UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

Author keywords

Cirrhosis; Glutathione peroxidase; Selenium; Thioacetamide; Thioredoxin reductase

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; GLUTATHIONE PEROXIDASE; LIVER ENZYME; THIOACETAMIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DISEASE COURSE; ENZYME ACTIVITY; LIVER CIRRHOSIS; MALE; MOUSE; NONHUMAN; OXIDATIVE STRESS; VITAMIN SUPPLEMENTATION;

ALANINE TRANSAMINASE; ANIMALS; ASPARTATE AMINOTRANSFERASES; BIOLOGICAL AVAILABILITY; DIET; DIETARY SUPPLEMENTS; GLUTATHIONE PEROXIDASE; LIVER; LIVER CIRRHOSIS; MALE; MICE; OXIDATIVE STRESS; SELENIUM; THIOACETAMIDE; THIOREDOXIN; THIOREDOXIN REDUCTASE (NADPH);

MUS;

EID: 34548639340     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2007.06.013     Document Type: Article

References (44)

1. Abul H., Mathew T.C., Dashti H.M., and Al-Bader A. Level of superoxide dismutase, glutathione peroxidase and uric acid in thioacetamide-induced cirrhotic rats. Anat. Histol. Embryol. 31 (2002) 66-71
2. Al-Bader A., Abul H., Hussain T., Al-Moosawi M., Mathew T.C., and Dashti H. Selenium and liver cirrhosis. Mol. Cell. Biochem. 185 (1998) 1-6
3. Agay D., Anderson R.A., Sandre C., Bryden N.A., Alonso A., Roussel A.M., and Chancerelle Y. Alterations of antioxidant trace elements (Zn, Se, Cu) and related metallo-enzymes in plasma and tissues following burn injury in rats. Burns 31 (2005) 366-371
4. Arner E.S.J., and Holmgren A. Physiological functions of thioredoxin and thioredoxin reductase. Eur. J. Biochem. 267 (2000) 6102-6109
5. Banning A., Deubel S., Kluth D., Zhou Z.W., and Brigelius-Flohe R. The GI-GPx gene is a target for Nrf2. Mol. Cell. Biol. 25 (2005) 4914-4923
6. Buljevac M., Romic Z., Vucelic B., Banic M., Krznaric Z., and Plesko S. Serum selenium concentration in patients with liver cirrhosis and hepatocellular carcinoma. Acta Med. Croat. 50 (1996) 11-14
7. Burk R.F., Early D.S., Hill K.E., Palmer I.S., and Boeglin M.E. Plasma selenium in patients with cirrhosis. Hepatology 27 (1998) 794-798
8. Chen Z.H., Saito Y., Yoshida Y., Sekine A., Noguchi N., and Niki E. 4-Hydroxynonenal induces adaptive response and enhances PC12 cell tolerance primarily through induction of thioredoxin reductase 1 via activation of Nrf2. J. Biol. Chem. 280 (2005) 41921-41927
9. Cheng W.H., Ho Y.S., Ross D.A., Valentine B.A., Combs G.F., and Lei X.G. Cellular glutathione peroxidase knockout mice express normal levels of selenium-dependent plasma and phospholipid hydroperoxide glutathione peroxidases in various tissues. J. Nutr. 127 (1997) 1445-1450
10. Czuczejko J., Zachara B.A., Staubach-Topczewska E., Halota W., and Kedziora J. Selenium, glutathione and glutathione peroxidases in blood of patients with chronic liver diseases. Acta Biochim. Pol. 50 (2003) 1147-1154
11. Das K.C., Guo X.L., and White C.W. Induction of thioredoxin and thioredoxin reductase gene expression in lungs of newborn primates by oxygen. Am. J. Physiol. 276 (1999) L530-L539
12. Dworkin B., Rosenthal W.S., Jankowski R.H., Gordon G.G., and Haldea D. Low blood selenium levels in alcoholics with and without advanced liver disease. Correlations with clinical and nutritional status. Dig. Dis. Sci. 30 (1985) 838-844
13. Dworkin B.M., Rosenthal W.S., Stahl R.E., and Panesar N.K. Decreased hepatic selenium content in alcoholic cirrhosis. Dig. Dis. Sci. 33 (1988) 1213-1217
14. Ellman G.L. Tissue sulfhydryl groups. Arch. Biochem. Biophys. 82 (1959) 70-77
15. Ekstrom G., and Ingelman-Sundberg M. Rat liver microsomal NADPH-supported oxidase activity and lipid peroxidation dependent on ethanol-inducible cytochrome P-450 (P-450IIE1). Biochem. Pharmacol. 38 (1989) 1313-1319
16. Hintze K.J., Keck A.S., Finley J.W., and Jeffery E.H. Induction of hepatic thioredoxin reductase activity by sulforaphane, both in Hepa1c1c7 cells and in male Fisher 344 rats. J. Nutr. Biochem. 14 (2003) 173-179
17. Hirota K., Nakamura H., Arai T., Ishii H., Bai J., Itoh T., Fukuda K., and Yodoi J. Geranylgeranylacetone enhances expression of thioredoxin and suppresses ethanol-induced cytotoxicity in cultured hepatocytes. Biochem. Biophys. Res. Commun. 275 (2000) 825-830
18. Jacobson G.A., Narkowicz C., Tong Y.C., and Peterson G.M. Plasma glutathione peroxidase by ELISA and relationship to selenium level. Clin. Chim. Acta 369 (2006) 100-103
19. Lee J.W., Shin K.D., Lee M., Kim E.J., Han S.S., Han M.Y., Ha H., Jeong T.C., and Koh W.S. Role of metabolism by flavin-containing monooxygenase in thioacetamide-induced immunosuppression. Toxicol. Lett. 136 (2003) 163-172
20. Navarro-Alarcon M., de la Serrana H.L.G., Perez-Valero V., and Lopez-Martinez M.C. Selenium concentrations in serum of individuals with liver diseases (cirrhosis or hepatitis): relationship with some nutritional and biochemical markers. Sci. Total Environ. 291 (2002) 135-141
21. Nelson R.L., Davis F.G., Sutter E., Kikendall J.W., Sobin L.H., Milner J.A., and Bowen P.E. Serum selenium and colonic neoplastic risk. Dis. Colon Rectum 38 (1995) 1306-1310
22. Ohkawa H., Ohishi N., and Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 95 (1979) 351-358
23. Olson O.E., Palmer I.S., and Cary E.E. Modification of official fluorometric method for selenium in plants. J. Assoc. Off. Anal. Chem. 58 (1975) 117-121
24. Okuyama H., Nakamura H., Shimahara Y., Araya S., Kawada N., Yamaoka Y., and Yodoi J. Overexpression of thioredoxin prevents acute hepatitis caused by thioacetamide or lipopolysaccharide in mice. Hepatology 37 (2003) 1015-1025
25. Okuyama H., Shimahara Y., Nakamura H., Araya S., Kawada N., Yamaoka Y., and Yodoi J. Thioredoxin prevents thioacetamide-induced acute hepatitis. Comp. Hepatol. 3 (2004) S1-S6
26. Okuyama H., Nakamura H., Shimahara Y., Uyama N., Kwon Y.W., Kawada N., Yamaoka Y., and Yodoi J. Overexpression of thioredoxin prevents thioacetamide-induced hepatic fibrosis in mice. J. Hepatol. 42 (2005) 117-123
27. Pan M., Song Y.L., Xu J.M., and Gan H.Z. Melatonin ameliorates nonalcoholic fatty liver induced by high-fat diet in rats. J. Pineal Res. 41 (2006) 79-84
28. Papp L.V., Lu J., Striebel F., Kennedy D., Holmgren A., and Khanna K.K. The redox state of SECIS binding protein 2 controls its localization and selenocysteine incorporation function. Mol. Cell. Biol. 26 (2006) 4895-4910
29. Park Y.S., Misonou Y., Fujiwar N., Takahashi M., Miyamoto Y., Koh Y.M., Suzuki K., and Taniguch N. Induction of thioredoxin reductase as an adaptive response to acrolein in human umbilical vein endothelial cells. Biochem. Biophys. Res. Commun. 327 (2005) 1058-1065
30. Perocco P., Bronzetti G., Canistro D., Valgimigli L., Sapone A., Affatato A., Pedulli G.F., Pozzetti L., Broccoli M., Iori R., Barillari J., Sblendorio V., Legator M.S., Paolini M., and Abdel-Rahman S.Z. Glucoraphanin, the bioprecursor of the widely extolled chemopreventive agent sulforaphane found in broccoli, induces phase-I xenobiotic metabolizing enzymes and increases free radical generation in rat liver. Mutat. Res. 595 (2006) 125-136
31. Rayman M.P. The importance of selenium to human health. Lancet 356 (2000) 233-241
32. Reeves P.G., Leary P.D., Gregoire B.R., Finley J.W., Lindlauf J.E., and Johnson L.K. Selenium bioavailability from buckwheat bran in rats fed a modified AIN-93G torula yeast-based diet. J. Nutr. 135 (2005) 2627-2633
33. Rivera C.A., Bradford B.U., Hunt K.J., Adachi Y., Schurum L.W., Koop D.R., Burchardt E.R., Rippe R.A., and Thurman R.G. Attenuation of CCl4-induced hepatic fibrosis by GdCl3 treatment or dietary glycine. Am. J. Physiol.-Gastroint. Liver Physiol. 281 (2001) G200-G207
34. Rotruck J.T., Pope A.L., Ganther H.E., Swanson A.B., Hafeman D.G., and Hoekstra W.G. Selenium: biochemical role as a component of glutathione peroxidase. Science 179 (1973) 588-590
35. Sakurai A., Yuasa K., Shoji Y., Himeno S., Tsujimoto M., Kunimoto M., Imura N., and Hara S. Overexpression of thioredoxin reductase I regulates NF-kappa B activation. J. Cell. Physiol. 198 (2004) 22-30
36. Saitoh M., Nishitoh H., Fujii M., Takeda K., Tobiume K., Sawada Y., Kawabata M., Miyazono K., and Ichijo H. Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1. EMBO J. 17 (1998) 2596-2606
37. Soylu A.R., Altaner S., Aydogdu N., Basaran U.N., Tarcin O., Gedik N., Umit H., Tezel A., Ture M., Kutlu K., and Kaymak K. Effects of vitamins E and C supplementation on hepatic glutathione peroxidase activity and tissue injury associated with ethanol ingestion in malnourished rats. Curr. Ther. Res.-Clin. Exp. 67 (2006) 118-137
38. Valimaki M., Alfthan G., Vuoristo M., and Ylikahri R. Effects of selenium supplementation on blood and urine selenium levels and liver function in patients with primary biliary cirrhosis. Clin. Chim. Acta 196 (1991) 7-15
39. Van-Gossum A., and Neve J. Low selenium status in alcoholic cirrhosis is correlated with aminopyrine breath test. Preliminary effects of selenium supplementation. Biol. Trace Elem. Res. 47 (1995) 201-207
40. Wang H.L., Zhang J.S., and Yu H.Q. Elemental selenium at nano size (Nano-Se) possesses lower toxicity without compromising the fundamental effect on selenoenzymes: comparison with selenomethionine in mice. Free Radic. Biol. Med. 42 (2007) 1524-1533
41. Weiss S.L., Evenson J.K., Thompson K.M., and Sunde R.A. Dietary selenium regulation of glutathione peroxidase mRNA and other selenium-dependent parameters in male rats. J. Nutr. Biochem. 8 (1997) 85-91
42. Yang J.G., Morrison-Plummer J., and Burk R.F. Purification and quantitation of a rat plasma selenoprotein distinct from glutathione peroxidase using monoclonal antibodies. J. Biol. Chem. 262 (1987) 13372-13375
43. Zachara B.A., Pawluk H., Bloch-Boguslawska E., Sliwka K.M., Korenkiewicz J., Skok Z., and Ryc K. Tissue level, distribution, and total body selenium content in healthy humans and in some diseases in Poland. Arch. Environ. Health 56 (2001) 461-466
44. Zhang J.S., Ma K.Y., and Wang H.L. Cyclophosphamide suppresses thioredoxin reductase in bladder tissue and its adaptive response via inductions of thioredoxin reductase and glutathione peroxidase. Chem. Biol. Interact. 162 (2006) 24-30