Enhanced antioxidant defense due to extracellular catalase activity in Syrian hamster during arousal from hibernation

Comparative Biochemistry and Physiology - C Toxicology and Pharmacology

Volumn 143, Issue 4, 2006, Pages 484-491

  Ohta, Hitomi ^a   Okamoto, Iwao ^a   Hanaya, Toshiharu ^a   Arai, Shigeyuki ^a   Ohta, Tsunetaka ^a   Fukuda, Shigeharu ^a  

^a HAYASHIBARA BIOCHEMICAL LABORATORIES INC   (Japan)

Author keywords

Antioxidants; Catalase; Glutathione; Glutathione peroxidase; Hamster; Hibernation; Hydrogen peroxide; Ischemia; Reperfusion

Indexed keywords

AMINOTRIAZOLE; CATALASE; GLUTATHIONE PEROXIDASE; HYDROGEN PEROXIDE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANTIOXIDANT ACTIVITY; AROUSAL; ARTICLE; CELL PROTECTION; CONTROLLED STUDY; CYTOTOXICITY; DEFENSE MECHANISM; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; ENZYME INHIBITION; ENZYME PURIFICATION; EXTRACELLULAR MATRIX; FEMALE; HIBERNATION; HYPOTHERMIA; MEDICAL ASSESSMENT; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RAT; RECTUM TEMPERATURE; SPECIES COMPARISON; SYRIAN HAMSTER;

ANIMALIA; CRICETINAE; MAMMALIA; MESOCRICETUS AURATUS;

EID: 33746039663     PISSN: 15320456     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpc.2006.05.002     Document Type: Article

References (41)

1. 3H]thymidine incorporation assay. J. Immunol. Methods 170 (1994) 211-224
2. Amstad P., Peskin A., Shah G., Mirault M., Moret R., Zbinden I., and Cerutti P. The balance between Cu,Zu-superoxide dismutase and catalase affects the sensitivity of mouse epidermal cells to oxidative stress. Biochemistry 30 (1991) 9305-9313
3. Arai S., Hanaya T., Sakurai T., Ikeda M., and Kurimoto M. A novel phenomenon predicting the entry into a state of hibernation in Syrian hamsters (Mesocricetus auratus). J. Vet. Med. Sci. 67 (2005) 215-217
4. Baud O., Greene A.E., Li J., Wang H., Volpe J.J., and Rosenberg P.A. Glutathione peroxidase-catalase cooperativity is required for resistance to hydrogen peroxide by mature rat oligodendrocytes. J. Neurosci. 24 (2004) 1531-1540
5. Bron A.M., Maupoil V., Garcher C., Guyonnet G., Chelqi E.H., and Rochette L. Modification of vitamin E during ischemia-reperfusion in rat retina. Invest. Ophthalmol. Vis. Sci. 36 (1995) 1084-1087
6. Buzadzic B., Spasic M., Saicic Z.S., Radojicic R., Halliwell B., and Petrovic V.M. Antioxidant defenses in the ground squirrel Citellus citellus: 1. A comparison with the rat. Free Radic. Biol. Med. 65 (1972) 401-406
7. Carey H., Sills N., and Gorham D.A. Stress proteins in mammalian hibernation. Am. Zool. 39 (1999) 825-835
8. Carey H.V., Frank C.L., and Seifert J.P. Hibernation induces oxidative stress and activation of NK-kappaB in ground squirrel intestine. J. Comp. Physiol., B 170 (2000) 551-559
9. Carey H.V., Andrews M.T., and Martin S.L. Mammalian hibernation: cellular and molecular responses to depressed metabolism and low temperature. Physiol. Rev. 83 (2003) 1153-1181
10. +-ATPase in the red blood cells of the hibernating black bear. Life Sci. 71 (2002) 153-161
11. Clement M.V., Ramalingam J., Long L.H., and Halliwell B. The in vitro cytotoxicity of ascorbate depends on the culture medium used to perform the assay and involves hydrogen peroxide. Antioxid. Redox Signal. 3 (2001) 157-163
12. Cooper A.J., Pulsinelli W.A., and Duffy T.E. Glutathione and ascorbate during ischemia and postischemic reperfusion in rat brain. J. Neurochem. 35 (1980) 1242-1245
13. Dorfman L.M., and Adams G.E. Reactivity of the hydroxyl radical in aqueous solutions. National Standard Reference System. Monograph NSRDS-NBS vol. 46 (1973), National Bureau of Standards 1-59
14. Drew K.L., Osborne P.G., Frerichs K.U., Hu Y., Koren R.E., Hallenbeck J.M., and Rice M.E. Ascorbate and glutathione regulation in hibernating ground squirrels. Brain Res. 94 (1999) 1-8
15. Drew K.L., Toien O., Rivera P.M., Smith M.A., Perry G., and Rice M.E. Role of the antioxidant ascorbate in hibernation and warming from hibernation. Comp. Biochem. Physiol., C 133 (2002) 483-492
16. Dringen R., and Hamprecht B. Involvement of glutathione peroxidase and catalase in the disposal of exogenous hydrogen peroxide by cultured astroglial cells. Brain Res. 759 (1997) 67-75
17. Ghosh S., Janocha A.J., Aronica M.A., Swaidani S., Comhair S.A.A., Xu W., Zheng L., Kaveti S., Kinter M., Hazen S.L., and Erzurum S.C. Nitrotyrosine proteome survey in asthma identifies oxidative mechanism of catalase inactivation. J. Immunol. 176 (2006) 5587-5597
18. Halliwell B. Reactive oxygen species and the central nervous system. J. Neurochem. 59 (1992) 1609-1623
19. Halliwell B., and Gutteridge J.M. The antioxidants of human extracellular fluids. Arch. Biochem. Biophys. 280 (1990) 1-8
20. Halliwell, B., Gutteridge, J.M.C., 1999. Antioxidant defence enzymes: the glutathione peroxidase family. Free radicals in biology and medicine. Ed 3, 140-146, 170-172.
21. Hermes-Lima M., and Zenteno-Savin T. Animal response to drastic changes in oxygen availability and physiological oxidative stress. Comp. Biochem. Physiol., C 133 (2002) 537-556
22. Hermes-Lima M., Storey J., and Storey K.B. Antioxidant defenses and animal adaptation. In: Storey K., and Storey J.M. (Eds). Protein Adaptations and Signal Transduction (2001), Elsevier 263-287
23. 2-induced apoptosis in PC12 cells by glutathione independent mechanism. Neurosci. Lett. 14 (1995) 179-182
24. Lee A.S. Mammalian stress response: induction of the glucose-regulated protein family. Curr. Opin. Cell Biol. 4 (1992) 267-273
25. Li Y., Maher P., and Schubert D. A role for 12-lipoxygenase in nerve cell death caused by glutathione depletion. Neuron 19 (1997) 453-463
26. Lyman C.P. The oxygen consumption and temperature regulation of hibernating hamsters. J. Exp. Zool. 109 (1948) 55-78
27. Lyman C.P. Oxygen consumption, body temperature and heart rate of woodchucks entering hibernation. Am. J. Physiol. 194 (1958) 83-91
28. Martin R., Montero C., Mostaza J.M., Lopez J.L., Argomaniz L., Llorente P., and Martin L. Urate production in a porcine model of myocardial ischemia-reperfusion. Rev. Esp. Cardiol. 49 (1996) 281-287
29. Masters C., and Crane D. Isozymes and the micro organization of organellar structure and function. Prog. Clin. Biol. Res. 344 (1990) 101-122
30. Moonyong L., Inho C., and Kyoungsook P. Activation of stress signaling molecules in bat brain during arousal from hibernation. J. Neurochem. 82 (2002) 867-873
31. Nedergaard J., and Cannon B. Mammalian hibernation. Philos. Trans. R. Soc. Lond. Biol. 326 (1990) 669-685
32. Nurnberger F. The neuroendocrine system in hibernating mammals: present knowledge and open questions. Cell Tissue Res. 281 (1995) 391-412
33. Osborne P.G., and Hashimoto M. State-dependent regulation of cortical blood flow and respiration in hamsters: response to hypercapnia during arousal from hibernation. J. Physiol. 547 (2003) 963-970
34. Osborne P.G., and Hashimoto M. Brain antioxidant levels in hamsters during hibernation, arousal and cenothermia. Behav. Brain Res. 168 (2006) 208-214
35. Peterkofsky B., and Parather W. Cytotoxicity of ascorbate and other reducing agents towards cultured fibroblasts as a result of hydrogen peroxide formation. J. Cell. Physiol. 90 (1977) 61-70
36. Sandstrom P.A., and Buttke T.M. Autocrine production of extracellular catalase prevents apoptosis of the human CEM T-cell line in serum-free medium. Proc. Natl. Acad. Sci. U. S. A. 90 (1993) 4708-4712
37. Storey K.B. Adventure in oxygen metabolism. Comp. Biochem. Physiol., B 139 (2004) 359-369
38. Tandon R., Khanna H.D., and Dorababu M. Oxidative stress and antioxidants status in peptic ulcer and gastric carcinoma. Indian J. Physiol. Pharmacol. 48 (2004) 115-118
39. Toien O., Drew K., Chao M., and Rice M.E. Ascorbate dynamics and oxygen consumption during arousal from hibernation in Arctic ground squirrels. Am. J. Physiol. 281 (2001) R1-R11
40. Varadharaj S., Watkins T., Cardounel A.J., Garcia J.G.N., Zweier J.L., Kuppusamy P., Natarajan V., and Parinandi N.L. Vitamin C-induced loss of redox-dependent viability in lung microvascular endothelial cells. Antioxid. Redox Signal. 7 (2005) 287-300
41. Yakes F.M., and Van Houten B. Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress. Proc. Natl. Acad. Sci. U. S. A. 94 (1997) 514-519