PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2006 | 15 | 6 |

Tytuł artykułu

Glutathione-related enzyme activity in liver and kidney of rats exposed to cadmium and ethanol

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The activity of glutathione peroxidase (GPx), glutathione reductase (GR) and glutathione S-transferase (GST) was investigated in liver and kidney of rats exposed to cadmium (Cd) and ethanol (EtOH) alone and in combination. Rats were treated with 50 mg Cd/dm3 in drinking water and/or 5 g of EtOH/kg body wt/24 h intragastrically, for 12 weeks. Exposure to Cd led to an increase in GPx and GST activity with a simultaneous decrease in GR activity in the liver. In the kidney of rats treated with Cd, an increase in the activity of GPx and GR was noted. In the EtOH-exposed rats, GPx activity decreased in the liver, but increased in the kidney. Exposure to EtOH caused a reduction in GR activity only in the liver. The co-exposure to Cd and EtOH led to an increase in the liver and kidney GPx activity compared to control. In the rats simultaneously exposed to Cd and EtOH liver activity of GR decreased compared to control, whereas the kidney GR activity increased compared to control as well as to the groups treated with Cd and EtOH seperately. The co-exposure to Cd and EtOH led to an increase in the liver activity of GST compared to the control and EtOH groups. Analysis of variance (ANOVA/MANOVA) revealed that the changes noted in the activity of investigated enzymes in the Cd + EtOH group resulted from the independent action of both Cd or EtOH as well as from their interactive ac­tion. Numerous correlations (negative or positive) were noted between the activity of GPx, GR and GST, and the concentration of GSH, Cd and MDA in the liver and kidney. On the basis of our results it can be concluded that changes in the activity of GPx, GR and GST in the liver and kidney may be involved in the mechanism leading to a decrease in GSH concentration in these organs due to exposure to Cd and EtOH alone and in conjunction with each other.

Wydawca

-

Rocznik

Tom

15

Numer

6

Opis fizyczny

p.861-868,fig.,ref.

Twórcy

autor
  • Medical University of Bialystok, Mickiewicza 2c, 15-222 Bialystok, Poland
autor

Bibliografia

  • 1. CASALINO E., CALZARETTI G., SBLANO C., LANDRISCINA C. Molecular inhibitory mechanism of antioxidant enzymes in rat liver and kidney by cadmium. Toxicology 179, 37, 2002.
  • 2. SHAIKH Z. A., VU T. T., ZAMAN K. Oxidative stress as a mechanism of chronic cadmium-induced hepatotoxicity and renal toxicity and protection by antioxidants. Toxicol. Appl. Pharmacol. 154, 256, 1999.
  • 3. STOHS S. J., BAGCHI D., HASSOUN E., BAGCHI M. Oxidative mechanisms in the toxicity of chromium and cadmium ions. J. Environ. Pathol. Toxicol. Oncol. 19, 201, 2000.
  • 4. JURCZUK M., MONIUSZKO-JAKONIUK J., BRZÓSKA M. M., ROSZCZENKO A. Vitamins E and C concentrations in the liver and kidney of rats exposed to cadmium and ethanol. Pol. J. Environ. Stud. 14, 599, 2005.
  • 5. THURMAN R. G., BRADFORD B. U., IIMURO Y., FRANKENBERG M. V., KNECHT K. T., CONNOR H. D., ADACHI Y., WALL C., ARTEEL G. E., RAIEIGH J. A., FORMAN D. T., MASON R. P. Mechanism of alcohol-in­duced hepatotoxicity: studies in rats. Front. Biosci. 4, 42, 1999.
  • 6. WIŚNIEWSKA-KNYPL J. M., WROŃSKA-NOFER T. Biological markers of oxidative stress induced by ethanol and iron overload in rats. Int. J. Occup. Med. Environ Health 7, 355, 1994.
  • 7. JURCZUK M., MONIUSZKO-JAKONIUK J., BRZÓSKA M. M., ROGALSKA J., ROSZCZENKO A., KULIKOWS- KA-KARPIŃSKA E. Evaluation of chosen parameters of oxidative stress in rats exposed to lead and ethanol. Pol. J. Environ. Stud. 12, 187, 2003.
  • 8. JURCZUK M., BRZÓSKA M. M., MONIUSZKO-JAKO- NIUK J., GAŁAŻYN-SIDORCZUK M., KULIKOWSKA- KARPIŃSKA E. Antioxidant enzymes activity and lipid peroxidation in liver and kidney of rats exposed to cadmium and ethanol. Food Chem. Toxicol. 42, 429, 2004.
  • 9. MONIUSZKO-JAKONIUK J., JURCZUK M., BRZÓSKA M. M., ROGALSKA J., GAłAŻYN-SIDORCZUK M. In­volvement of some low-molecular thiols in the destructive mechanism of cadmium and ethanol action on rat livers and kidneys. Pol. J. Environ. Stud. 14, 483, 2005.
  • 10. HUSAIN K., SCOTT B. R., REDDY S. K., SOMANI S. M. Chronic ethanol and nicotine interaction on rat tissue anti- oxidant defense system. Alcohol 25, 89, 2001.
  • 11. DENEKE S. Thiol-based antioxidants. Curr. Top. Cell Reg. 36, 151, 2000
  • 12. PARKE D. V., PIOTROWSKI J. Glutathione: Its role in detoxication of reactive oxygen and environmental chemicals. Acta Pol. Toxicol. 4, 1, 1996
  • 13. ARAI M., IMAI H., KOUMURA T., YOSHIDA M., EMO- TO K., UMEDA M. et al. Mitochondrial phospholipid hy­droperoxide glutathione peroxidase plays a major role in preventing oxidative injury to cells. J. Biol. Chem. 274, 4924, 1999.
  • 14. DRINGER A. Metabolism and function of glutathione in brain. Progress in Neurobiol. 62, 649, 2000.
  • 15. REED D. J. Glutathione: Toxicological implications. Ann. Rev. Pharmacol. Toxicol. 30, 603, 1990.
  • 16. STRANGE R. C., JONES P. W., FRYER A. A. Glutathione S-transferase: genetics and role in toxicology. Toxicol. Lett. 112-113, 357, 2000.
  • 17. BOON P. J., MARINHO H. S., OOSTING R., MULDER G. J. Glutathione conjugation of 4-hydroxy-trans-2.3-non- enal in the rat in vivo, the isolated perfused liver and erythrocytes. Toxicol. Appl. Pharmacol. 159, 214, 1999.
  • 18. LAURENT A., PERDU-DURAND E., ALARY J., DEB- RAUWER L., CRAVEDI J. P. Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat preci­sion-cut liver slices. Toxicol. Lett. 114, 203, 2000.
  • 19. CASALINO E., SBLANO C., LANDRISCINA C. Enzyme activity alteration by cadmium administration to rats: the possibillity of iron involvement in lipid peroxidation. Arch. Biochem. Biophys. 15, 171, 1997.
  • 20. KARMAKAR R., BANIK S., BANDYOPADHYAY S., CHATTERJEE M. Cadmium-induced alterations of hepatic lipid peroxidation, glutathione S-transferase activity and re­duced glutathione level and their possible correlation with chromosomal aberration in mice: a time course study. Mutat. Res. 397, 183, 1998.
  • 21. OH S. I., KIM CH. I., CHUN H. J., PARK S. CH. Chronic ethanol consumption affects glutathione status in rat liver. J. Nutr. 128, 758, 1998.
  • 22. SCOTT R. B., REDDY K. S., HUSAIN K., SCHLORFF E. C., RYBAK L. P., SOMANI S.M. Dose response of ethanol on antioxidant defence system of liver, lung, and kidney in rat. Pathophysiology 7, 25, 2000.
  • 23. SIVARAM A. G., SURESH M. V., INDRA M. Combined effect of ascorbic acid and selenium supplementation on al­cohol-induced oxidative stress in guinea pigs. Comp. Bio­chem. Physiol. Part C 134, 397, 2003.
  • 24. BRZÓSKA M. M., MONIUSZKO-JAKONIUK J. JURC­ZUK M., GAŁAŻYN-SIDORCZUK M. Cadmium turnover and changes of zinc and copper body status of rats continu­ously exposed to cadmium and ethanol. Alcohol Alcohol. 37, 213, 2002.
  • 25. CHALKLEY S. R., RICHMOND J., BARLTROP D. Mea­surement of vitamin D3 metabolites in smelter workers ex­posed to lead and cadmium. Occup. Environ. Med. 55, 446, 1998.
  • 26. WANG H., ZHU G., SHI Y., WENING S., JIN T., KONG Q., NORDBERG G. F. Influence of environmental cadmium exposure on forearm bone density. J. Bone Miner. Res. 18, 553, 2003.
  • 27. PETERSON G. L. A simplification of the protein assay method of Lowry et al, which is more generally applicable. Anal. Biochem. 83, 346, 1977.
  • 28. SEŃCZUK W. Toksykologia współczesna. PZWL, Warsza­wa, p. 158, 2005 (in Polish).
  • 29. BRIVIBA K., KLOTZ LO, SIES H. Defenses against per- oxynitrate. Methods Enzymol. 301, 301, 1999.
  • 30. DUPONT I., KLUCAS D., CLOT P., MENEZ C., ALBA- NO E. Cytochrome P4502E1 inducitibility and hydroxyeth- yl radical formation among alcoholics. J. Hepatol. 28, 564, 1998.
  • 31. POLAVARAPU R., SPITZ D. R., SIM J. E., et al. Increased lipid peroxidation and impaired antioxidant enzyme func­tion is associated with pathological liver injury In experi­mental alcoholic liver disease in rats fed diets high in corn oil and fish oil. Hepatology 27, 1317, 1998.
  • 32. ROUACH H., FATACCIOLI V., GENTIL M., FRENCH S. W., MORIMOTO M., NORDMANN R. Effect of chronic ethanol feeding on lipid peroxidation and protein oxidation in relation to liver pathology. Hepatology 25, 351, 1997.
  • 33. BAILEY S. M., PATEL V. B., YOUNG T. A., ASAYAMA K., CUNNINGHAM C. C. Chronic ethanol consumption alters the glutathione/glutathione peroxidase-1 system and protein oxidation status in rat liver. Alcohol Clin. Exp. Res. 25, 726, 2001.
  • 34. BARTOSZ G. Metabolizm glutationu. Post. Biochem. 39, 32, 1993. (in Polish).
  • 35. SALVEMINI F., FRAZE A., IERVOLINOA., FILOSA S., SALzANO S., URSINI M. V. Enhanced glutathione levels and oxidoresistance mediated by increased glucose-6-phos- phate dehydrogenase expression. J. Biol. Chem. 274, 2750, 1999.
  • 36. SZWEDA L. I., UCHIDA K., TASI L., STADTMAN E. R. Inactivation of glucose-6-phosphate dehydrogenase by 4- hydroxy-2-nonenal. J. Biol. Chem. 268, 3342, 1993.
  • 37. DANIEL V. Glutathione S-transferases: gene structure and regulation of expression. Crit. Rev. Biochem. Mol. Biol. 28, 173, 1993.
  • 38. BALLATORI N. Glutathione mercaptides as transport forms of metals. Adv. Pharmacol. 27, 3760, 1994.
  • 39. WANG W., BALLATORI N. Endogenous glutathione con­jugates: occurrence and biological function. Pharmacol. Rev. 50, 335, 1998.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-e852c977-01a0-487d-a5bd-d84fdfb6cd2a
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.