Tertiary butyl hydroperoxide induced oxidative damage in mice erythrocytes: Protection by taurine

Pathophysiology

Volumn 19, Issue 2, 2012, Pages 137-148

  Roy, Anandita ^a   Sil, Parames C ^a  

^a BOSE INSTITUTE   (India)

Author keywords

Alanine; Erythrocytes; Oxidative stress; ROS; Taurine; TBHP

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATE; BETA ALANINE; CALCIUM; CALPAIN; CATALASE; GLUTATHIONE; GLUTATHIONE DISULFIDE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; HEMOGLOBIN; METHEMOGLOBIN; METHEMOGLOBIN REDUCTASE; PHOSPHATIDYLSERINE; REACTIVE OXYGEN METABOLITE; TAURINE; TERT BUTYL HYDROPEROXIDE; THIOBARBITURIC ACID REACTIVE SUBSTANCE;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CELL LEVEL; CELL PROTECTION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG MECHANISM; ECHINOCYTE; ENZYME ACTIVITY; ENZYME REGULATION; ERYTHROCYTE; ERYTHROCYTE LEVEL; ERYTHROCYTE MEMBRANE; ERYTHROCYTE STRUCTURE; EXPOSURE; IN VITRO STUDY; LIPID PEROXIDATION; MEMBRANE STABILIZATION; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN CARBONYLATION; PROTEIN DEPLETION; SCANNING ELECTRON MICROSCOPY; UPREGULATION;

EID: 84861955030     PISSN: 09284680     EISSN: 1873149X     Source Type: Journal    
DOI: 10.1016/j.pathophys.2012.05.001     Document Type: Article

References (56)

1. Zavodnik L.B., Zavodnik I.B., Niekurzak A., Szosland K., Bryszewska M. Activation of red blood cell glutathione peroxidase and morphological transformation of erythrocytes under the action of tert-butyl hydroperoxide. Biochemistry and Molecular Biology International 1988, 44:577-588.
2. Rush G.F., Gorski J.R., Ripple M., Sowinski J., Bugelski P., Hewitt W. Organic hydroperoxide-induced lipid peroxidation and cell death in isolated hepatocytes. Toxicology and Applied Pharmacology 1985, 78:473-483.
3. Sarkar M.K., Sil P.C. Prevention of tertiary butyl hydroperoxide induced oxidative impairment and cell death by a novel antioxidant protein molecule isolated from the herb, Phyllanthus niruri. Toxicology In Vitro 2010, 24:1711-1719.
4. Bhattacharya S., Gachhui R., Sil P.C. Hepatoprotective properties of Kombucha tea against TBHP-induced oxidative stress via suppression of mitochondria dependent apoptosis. Pathophysiology 2011, 18:221-234.
5. Sarkar M.K., Kinter M., Mazumder B., Sil P.C. Purification and characterization of a novel antioxidant protein molecule from Phyllanthus niruri. Food Chemistry 2009, 114:1405-1412.
6. Deuticke B., Heller K.B., Haest W.M. Progressive oxidative membrane damage in erythrocytes after pulse treatment with t-butylhydroperoxide. Biochimica et Biophysica Acta 1987, 899:113-124.
7. Moore R.B., Brummitt M.L., Mankad V.N. Hydroperoxides selectively inhibit human erythrocyte membrane enzymes. Archives of Biochemistry and Biophysics 1989, 273:527-534.
8. Patterson L.K. Oxygen and Oxy-radicals in Chemistry and Biology, in Rodgers 1981, 89-94. Academic Press, New York. M.A.J., E.L. Powers (Eds.).
9. Mertens K., Rogiers V., Vercruysse A. Measurement of malondialdehyde in cultures of adult rat hepatocytes. Toxicology In Vitro 1990, 4:439-441.
10. Esterbauer H. Free Radicals, Lipid Peroxidation and Cancer 1982, 101-128. Academic Press, New York. D.C.H. McBrien, T.F. Slater (Eds.).
11. Benatti U., Morelli A., Damiani G., De Flora A. A methemoglobin-dependent and plasma-stimulated experimental model of oxidative hemolysis. Biochemical and Biophysical Research Communities 1982, 106:183-1190.
12. Cesquini M., Torsoni M.A., Stoppa G.R., Ogo S.H. t-BOOH-induced oxidative damage in sickle red blood cells and the role of flavonoids. Biomedicine and Pharmacotherapy 2003, 57:124-129.
13. Krukoski D.W., Comar S.R., Claro L.M., Leonart M.S., do Nascimento A.J. Effect of vitamin C, deferoxamine, quercetin and rutin against tert-butyl hydroperoxide oxidative damage in human erythrocytes. Hematology 2009, 14:168-172.
14. Das J., Ghosh J., Manna P., Sil P.C. Protective role of taurine against arsenic-induced mitochondria-dependent hepatic apoptosis via the inhibition of PKCdelta-JNK pathway. PLoS One 2010, 5:e12602.
15. Das J., Ghosh J., Manna P., Sil P.C. Arsenic-induced oxidative cerebral disorders: protection by taurine. Drug and Chemical Toxicology 2009, 32:93-102. (2009).
16. Das J., Ghosh J., Manna P., Sil P.C. Taurine protects rat testes against NaAsO(2)-induced oxidative stress and apoptosis via mitochondrial dependent and independent pathways. Toxicology Letters 2009, 187:201-210.
17. Ghosh J., Das J., Manna P., Sil P.C. Taurine prevents arsenic-induced cardiac oxidative stress and apoptotic damage: role of NF-kappa B, p38 and JNK MAPK pathway. Toxicology and Applied Pharmacology 2009, 240:73-87.
18. Manna P., Sinha M., Sil P.C. Taurine plays a beneficial role against cadmium-induced oxidative renal dysfunction. Amino Acids 2009, 36:417-428.
19. Manna P., Sinha M., Sil P.C. Amelioration of cadmium-induced cardiac impairment by taurine. Chemico-Biological Interactions 2008, 174:88-97.
20. Manna P., Sinha M., Sil P.C. Cadmium induced testicular pathophysiology: prophylactic role of taurine. Reproductive Toxicology 2009, 26:282-291.
21. Roy A., Manna P., Sil P.C. Prophylactic role of taurine on arsenic mediated oxidative renal dysfunction via MAPKs/NF-kappaB and mitochondria dependent pathways. Free Radical Research 2009, 43:995-1007.
22. Sinha M., Manna P., Sil P.C. Cadmium-induced neurological disorders: prophylactic role of taurine. Journal of Applied Toxicology 2008, 28:974-986.
23. Das J., Ghosh J., Manna P., Sil P.C. Taurine protects acetaminophen-induced oxidative damage in mice kidney through APAP urinary excretion and CYP2E1 inactivation. Toxicology 2010, 269:24-34.
24. Das J., Ghosh J., Manna P., Sil P.C. Acetaminophen induced acute liver failure via oxidative stress and JNK activation: protective role of taurine by the suppression of cytochrome P450 2E1. Free Radical Research 2010, 44:340-355.
25. Das J., Ghosh J., Manna P., Sil P.C. Taurine suppresses doxorubicin-triggered oxidative stress and cardiac apoptosis in rat via up-regulation of PI3-K/Akt and inhibition of p53, p38-JNK. Biochemical Pharmacology 2011, 81:891-909.
26. Das J., Ghosh J., Manna P., Sil P.C. Taurine provides antioxidant defense against NaF-induced cytotoxicity in murine hepatocytes. Pathophysiology 2008, 15:181-190.
27. Lu P., Xu W., Sturman J.A. Dietary β-alanine results in taurine depletion and cerebellar damage in adult cats. Journal of Neurology Research 1996, 43:112-119.
28. Sinha M., Manna P., Sil P.C. Taurine protects antioxidant defense system in the erythrocytes of cadmium treated mice. BMB Report 2008, 41:657-663.
29. Dawson R., Biasetti M., Messina S., Dominy J. The cytoprotective role of taurine in exercise-induced muscle injury. Amino Acids 2002, 22:309-324.
30. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 1976, 72:248-254.
31. Sinha M., Manna P., Sil P.C. Induction of necrosis in cadmium-induced hepatic oxidative stress and its prevention by the prophylactic properties of taurine. Journal of Trace Elements in Medicine and Biology 2009, 23:300-313.
32. Uchida K., Stadtman E.R. Covalent attachment of 4-hydroxynonenal to glyceraldehydes-3-phosphate dehydrogenase. Journal of Biological Chemistry 1993, 268:6388-6393.
33. Sinha M., Manna P., Sil P.C. Taurine, a conditionally essential amino acid, ameliorates arsenic-induced cytotoxicity in murine hepatocytes. Toxicology In Vitro 2007, 21:1419-1428.
34. Lee C.Y. Glucose-6-phosphate dehydrogenase from mouse. Methods in Enzymology 1982, 89:252-257.
35. Choury D., Kaplan J.C. Diaphorase P: a new fetal isozyme identified in human placenta. Biochimica et Biophysica Acta 1980, 613:18-25.
36. Kazennov A.M., Maslova M.N., Matskevich Y.A., Rustamov F.A., Shalabodov A.D. Species variability of erythrocyte transport ATPases in mammals. Comparative Biochemistry and Physiology. B: Comparative Biochemistry 1998, 119:169-175.
37. Ellman G.L. Tissue sulphydryl group. Archives of Biochemistry and Biophysics 1959, 82:70-77.
38. Hissin P.J., Hilf R.A. A fluorometric method for determination of oxidized and reduced glutathione in tissues. Analytical Biochemistry 1976, 74:214-226.
39. Manna P., Ghosh J., Das J., Sil P.C. Streptozotocin induced activation of oxidative stress responsive splenic cell signaling pathways: protective role of arjunolic acid. Toxicology and Applied Pharmacology 2010, 244:114-129.
40. Hoffman R., Benz E., Shattil S., Furie B., Cohen H. Hematology Basic Principles and Practice 2005, Churchill Livingstone, New York. 4th ed.
41. Mansouri A., Lurie A.A. Concise review: methemoglobinemia. American Journal of Hematology 1993, 42:7-12.
42. Grelloni F., Gabbianelli R., Falcioni G. Inactivation of glutathione peroxidase following hemoglobin oxidation. IUBMB Life 1991, 25:789-795.
43. Almar L., Otero C.S., Gallego J.G. Liver glutathione content and glutathione-dependent enzymes of two species of freshwater fish as bioindicators of chemical pollution. Journal of Environmental Science and Health 1998, 33:769-783.
44. Chance B., Sies H., Boveris A. Hydroperoxide metabolism in mammalian organs. Physiological Reviews 1979, 59:527-605.
45. Pon L.A., Schon E.A. Methods in Cell Biology 2007, vol. 80. Academic Press Publication, San Diego, California, pp. 379-393.
46. Handin R.I., Lux S.E., Stossel T.P. Blood: Principles and practice of hematology 1995, J.B. Lippincott Company, Philadelphia, PA, pp. 1921-1922.
47. Tuttle S., Stamato T., Perez M.L., Biaglow J. Glucose-6-phosphate dehydrogenase and the oxidative pentose phosphate cycle protect cells against apoptosis induced by low doses of ionizing radiation. Radiation Research 2000, 153:781-787.
48. Martín C., Martínez R., Navarro R., Ruiz-Sanz J.I., Lacort M., Larrea M.B. tert-Butyl hydroperoxide-induced lipid signaling in erythrocytes: involvement of glutathione and free radicals. Biochemical Pharmacology 2001, 62:705-712.
49. Berg C.P., Engels I.H., Rothbart A., Lauber K., Renz A., Schlosser S.F., Schulze-Osthoff K., Wesselborg S. Human mature red blood cells express caspase-3 and caspase-8, but are devoid of mitochondrial regulators of apoptosis. Cell Death and Differentiation 2001, 8:1197-1206.
50. Caprari P., Bozzi A., Malorni W., Bottini A., Iosi F., Santini M.T., Salvati A.M. Junctional sites of erythrocyte skeletal proteins are specific targets of tert-butylhydroperoxide oxidative damage. Chemico-Biological Interactions 1995, 94:243-258.
51. Bessis M. Blood Smears Reinterpreted 1977, Springer-Verlag, Berlin, pp. 50-52, 64.
52. Goldstein L., Brill S.R. Volume-activated taurine efflux from skate erythrocytes: possible band 3 involvement. American Journal of Physiology - Regulatory Integrative and Comparative Physiology 1991, 260:1014-1020.
53. Bratosin D., Estaquier F., Petit F., Arnoult D., Quatannens B., Tissier J.P., Slomianny C., Sartiaux C., Alonso C., Huart J.-J., Montreuil J., Ameisen J.C. Programmed cell death inmature erythrocytes: amodel for investigating death effector pathways operating in the absence of mitochondria. Cell Death and Differentiation 2001, 8:1143-1156.
54. 2+ influx into human red cells. Cell Calcium 1999, 26:131-137.
55. Cheville N.F. Ultrastructural Pathology, An Introduction to Interpretation 1994, Iwoa State University Press, Iwoa.
56. Shaffer J.E., Kocsis J.J. Methods of reducing tissue taurine levels. The Effects of Taurine Onexcitable Tissues 1981, 219-229. Spectrum Publications, New York. S.W. Schaffer, S.I. Baskin, J.J. Kocsis (Eds.).