Relationship between brain and liver oxidative state and maximum lifespan potential of different fish species

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 165, Issue 3, 2013, Pages 358-364

  Sanz, A ^a   Trenzado, C E ^a   Botello Castro, H ^a   Lopez Rodriguez M J ^a   Tierno de Figueroa, J M ^a  

^a UNIVERSITY OF GRANADA   (Spain)

Author keywords

Brain; Lipid peroxidation; Liver; Longevity; Oxidative state

Indexed keywords

CATALASE; DIHYDROLIPOAMIDE DEHYDROGENASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; MALONALDEHYDE; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN; CARP; CONTROLLED STUDY; ENZYME ACTIVITY; FISH; GOLDFISH; LIFESPAN; LIPID PEROXIDATION; LIVER; LUCIOBARBUS; LUCIOBARBUS SCLATERI; NONHUMAN; OXIDATIVE STRESS; RAINBOW TROUT; SQUALIUS; SQUALIUS PYRENAICUS;

EID: 84877829416     PISSN: 10956433     EISSN: 15314332     Source Type: Journal    
DOI: 10.1016/j.cbpa.2013.04.019     Document Type: Article

References (65)

1. Aebi H. Catalase in vitro. Method. Enzymol. 1984, 105:121-126.
2. Afanas'ev I. Signalling and damaging functions of free radicals in aging-free radical theory. Aging Dis. 2010, 1:75-88.
3. Barja G. The flux of free radical attack through mitochondrial DNA is related to aging rate. Aging Clin. Exp. Res. 2000, 12:342-355.
4. Barja G. Aging in vertebrates and the effect of caloric restriction: a mitochondrial free radical production-DNA damage mechanism?. Biol. Revs. 2004, 79:235-251.
5. Barja G. Radicales libres de origen mitocondrial y longevidad. An. Real Acad. Nac. Farm. 2005, 71(4):783-798.
6. Barja G., Herrero A. Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals. FASEB J. 2000, 14:312-318.
7. Buege J.A., Aust S.D. Microsomal lipid peroxidation. Meths. Enzymol. 1978, 52:302-310.
8. Buffenstein R., Edrey Y.H., Yang T., Mele J. The oxidative stress theory of aging: embattled or invincible? Insights from non-traditional model organisms. Age 2008, 30:99-109.
9. Calberg I., Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J. Biol. Chem. 1975, 250:5475-5480.
10. Carlsson L.M., Jonsson J., Edlund T., Marklund S.L. Mice lacking extracellular superoxide dismutase are more sensitive to hyperoxia. Proc. Natl. Acad. Sci. USA 1995, 92:6264-6268.
11. Couture P., Hulbert A.J. Membrane fatty acid composition of tissues is related to body mass of mammals. J. Membr. Biol. 1995, 148:27-39.
12. Duncan D.B. Multiple range and multiple F test. Biometrics 1955, 11:1-42.
13. Flohé L., Günzler W.A. Assay of glutathione peroxidase. Method. Enzymol. 1984, 105:115-121.
14. Franco Ruiz A., Rodríguez de los Santos M. Libro rojo de los vertebrados amenazados de Andalucía. Consejería de Medio Ambiente, Junta de Andalucía, Sevilla 2001.
15. Furné M., García-Gallego M., Hidalgo M.C., Morales A.E., Domezain A., Domezain J., Sanz A. Oxidative stress parameters during starvation and refeeding periods in Adriatic sturgeon (Acipenser naccarii) and rainbow trout (Oncorhynchu smykiss). Aquacult. Nutr. 2008, 15:587-595.
16. Gemma C., Vila J., Bachsetter A., Bickford P.C. Oxidative stress and the aging brain: from theory to prevention. Brain Aging: Models, Methods, and Mechanisms 2007, Frontiers in Neuroscience Series. CRC Press, Boca Raton, FL. D.R. Riddle (Ed.).
17. Gerschman R., Gilbert D.L., Nye S.W., Dwyer P., Fenn W.O. Oxygen poisoning and x-irradiation: a mechanism in common. Science 1954, 119:623-626.
18. Gulland J.A. Manual of sampling and statistical methods for fisheries biology. FAO, Rome 1966.
19. Gutteridge J.M.C., Quinlan G.J. Malondialdehyde formation from lipid peroxides in thiobarbituric acid test: the role of lipid radicals, iron salts, metal chelators. J. Appl. Biochem. 1983, 5:293-299.
20. Habig W.H., Pabst M.J., Jakoby W.B. Glutathione S-transferases-the first enzymatics tep in mercapturic acid formation. J. Biol. Chem. 1974, 249:7130-7139.
21. Halliwell B., Chirico S. Lipid peroxidation: its mechanism, measurement, and significance. Am. J. Clin. Nutr. 1993, 57:715-724.
22. Harman D. Aging: a theory based on free radical and radiation chemistry. J. Gerontol. 1956, 11:298-300.
23. Helfand S.L., Rogina B. Genetics of aging in the fruit fly, Drosophila melanogaster. Annu. Rev. Genet. 2003, 37:329-348.
24. Ho Y.S., Gargano M., Cao J., Bronson R.T., Heimler I., Hutz R.J. Reduced fertility in female mice lacking copper-zinc superoxide dismutase. J. Biol. Chem. 1998, 273:7765-7769.
25. Hoole D., Burgess B.P., Wellby I. Disease symptoms. Diseases of Carp and other Cyprinid Fishes 2001, Fishing News Books. Blackwell Science Ltd., London. D. Hoole, B.P. Burgess, I. Wellby (Eds.).
26. Huang T.T., Carlson E.J., Gillespie A.M., Shi Y., Epstein C.J. Ubiquitous overexpression of CuZn superoxide dismutase does not extend life span in mice. J. Gerontol. Ser. A-Biol. Sci. Med. Sci. 2000, 55:B5-B9.
27. Hulbert A.J. On the importance of fatty acid composition of membranes for aging. J. Theor. Biol. 2005, 234:277-288.
28. Hulbert A.J. The links between membrane composition, metabolic rate and lifespan. Comp. Biochem. Physiol. A 2008, 150:196-203.
29. Hulbert A.J., Pamplona R., Buffenstein R., Buttemer W.A. Life and death: Metabolic rate, membrane composition, and life span of animals. Physiol. Revs. 2007, 87:1175-1213.
30. Jena B.S., Nayak S.B., Patnaik B.K. Age-related changes in catalase activity and its inhibition by manganese (II) chloride in the brain of two species of poikilothermic vertebrates. Arch. Gerontol. Geriatr. 1998, 26:119-129.
31. Judge S., Judge A., Grune T., Leeuwenburgh C. Short-term CR decreases cardiac mitochondrial oxidant production but increases carbonyl content. Am. J. Physiol. 2004, 286:R254-R259.
32. Kitani K. Aging of the liver: facts and theories. Arch. Gerontol. Geriatr. 1991, 12:133-154.
33. Kottelat M., Freyhof J. Handbook of European freshwater fishes 2007, Publications Kottelat, Cornol.
34. Ku H.H., Brunk U.T., Sohal R.S. Relationship between mitochondrial superoxide and hydrogen peroxide production and longevity of mammalian species. Free Radic. Biol. Med. 1993, 15:621-627.
35. Leaver M.J., George S.G. A piscine glutathione S-transferase which efficiently conjugates the end-products of lipid peroxidation. Mar. Environ. Res. 1998, 46:71-74.
36. Lebel C.P., Bondy S.C. Oxidative damage and cerebral aging. Prog. Neurobiol. 1992, 38:601-609.
37. López- Torres M., Gredilla R., Sanz A., Barja G. Influence of aging and long-term caloric restriction on oxygen radical generation and oxidative DNA damage in rat liver mitochondria. Free Radic. Biol. Med. 2002, 32:882-889.
38. Marques F.Z., Markus M.A., Morris B.J. The molecular basis of longevity, and clinical implications. Maturitas 2010, 65:87-91.
39. Martínez-Álvarez R.M., Morales A.E., Sanz A. Antioxidant defenses in fish: biotic and abiotic factors. Rev. Fisher. Biol. Fish. 2005, 15:75-88.
40. McCord J.M., Fridovich J.M. Superoxide dismutase: an enzyme function for Erythrocuprein (Hemocuprein). J. Biol. Chem. 1969, 244:6049-6055.
41. Mockett R.J., Sohal R.S., Orr W.C. Over expression of glutathione reductase extends survival in transgenic Drosophila melanogaster under hyperoxia but not in normoxia. FASEB J. 1999, 13:1733-1742.
42. Montgomery M.K., Hulbert A.J., Buttemer W.A. Does the oxidative stress theory of aging explain longevity differences in birds? II. Antioxidant systems and oxidative damage. Exp. Gerontol. 2011, 47:211-222.
43. Ono T., Okada S. Unique increase in superoxide dismutase level in brains of long-living animals. Exp. Gerontol. 1984, 19:349-354.
44. Otto D.M.E., Moon T.W. Endogenous antioxidant systems of two teleost fish, the rainbowtrout and the blackbullhead, and the effect of age. Fish Physiol. Biochem. 1996, 15:349-358.
45. Page M.M., Richardson J., Wiens B.E., Tiedtke E., Peters C.W., Faure P.A., Burness G., Stuart J.A. Antioxidant enzyme activities are not broadly correlated with longevity in 14 vertebrate endotherm species. Age 2010, 33:33-47.
46. Pérez V., Buffenstein R., Masamsetti V., Leonard S., Salmon A. Protein stability and resistance to oxidative stress are determinants of longevity in the longest-living rodent, the naked mole-rat. Proc. Natl. Acad. Sci. USA 2009, 106:3059-3064.
47. Ramsey J.J., Hagopian K., Kenny T.M., Koomson E.K., Bevilacqua L., Weindruch R., Harper M.E. Proton leak and hydrogen peroxide production in liver mitochondria from energy-restricted rats. Am. J. Physiol. 2004, 286:E31-E40.
48. Reddy V.N., Giblin F.J., Lin L.R., Dang L., Unakar N.J., Musch D.C., Boyle D.L., Takemoto L.J., Ho Y.S., Knoernschild T., Juenemann A., Lutjen-Drecoll E. Glutathione peroxidase-1 deficiency leads to increased nuclear light scattering, membrane damage, and cataract formation in gene-knockout mice. Invest. Ophthalmol. Vis. Sci. 2001, 42:3247-3255.
49. Richter C.H., Park J.W., James B.N. Normal oxidative damage to mitochondrial and nuclear DNA is extensive Proc. Natl. Acad. Sci. USA 1988, 85:6465-6467.
50. Rudneva I. Antioxidant defense in marine fish and its relationship to their ecological status. Fish Ecology 2012, 31-59. Nova Science Publishers. Inc. Hauppauge NY, USA. S.P. Dempse (Ed.).
51. Sanz A., Hidalgo M.C., Morales A.E., Domenzain A., Domenzain J., García Gallego M. Evolution of antioxidant defenses and lipid peroxidation with age in the sturgeon Acipenser naccarii. Proceedings of the 4th International Symposium on Sturgeon, Oshkosh, Wisconsin, USA 2001, 89.
52. Sanz A., Furné M., Trenzado C.E., de Haro C., Sánchez-Muros M.J. Study of the oxidative state, as a marker of welfare, on gilthead sea bream (Sparus aurata) subjected to handling stress. J. World Aquacult. Soc. 2012, 43:707-715.
53. Sasaki T., Unno K., Tahara S., Shimada A., Chiba Y. Age-related increase of superoxide generation in the brains of mammals and birds. Aging Cell 2008, 7:459-469.
54. Schmucker D.L., Vessey R.K., Wang J.L., James F. Maloney age-dependent alterations in the physicochemical properties of rat liver microsomes. Mech. Ageing Dev. 1984, 27:207-217.
55. Sohal R.S., Brunk U.T. Mitochondrial production of prooxidants and cellular senescence. Mutat. Res. 1992, 275:295-304.
56. Sohal R.S., Orr W.C. Relationship between antioxidants, prooxidants, and the aging process. Ann. NY Acad. Sci. 1992, 663:74-84.
57. Sohal R.S., Sohal B.H., Brunk U.T. Relationship between antioxidant defenses and longevity in different mammalian species. Mech. Ageing Dev. 1990, 53:217-227.
58. Sohal R.S., Ku H.H., Agarwal S. Biochemical correlates of longevity in two closely related rodent species. Biochem. Biophys. Res. Commun. 1993, 196:7-11.
59. Sturve J., Stephensen E., Forlin L. Effects of redox cycling compounds on DT diaphorase activity in the liver of rainbow trout (Oncorhynchus mykiss). Comp. Hepatol. 2005, 4:4.
60. Tolmasoff J.M., Ono T., Cutler R.G. Superoxide dismutase: Correlation with life-span and specific metabolic rate in primate species. Proc. Natl. Acad. Sci. USA 1980, 77:2777-2781.
61. Trenzado C., Hidalgo C., García-Gallego M., Morales A.E., Furné M., Domenzain A., Domenzain J., Sanz A. Antioxidant enzymes and lipid peroxidation in sturgeon Acipenser naccarii and trout Oncorhynchus mykiss. A comparative study. Aquaculture 2006, 254:758-767.
62. Venn-Watson S., Smith C.R., Gomez F., Jensen E.D. Physiology of aging among healthy, older bottlenose dolphins (Tursiops truncatus): comparisons with aging humans. J. Comp. Physiol. B-Biochem. Syst. Environ. Physiol. 2011, 181:667-680.
63. Wdzieczak J., Zalesna G., Wujec E., Peres G. Comparative studies on superoxide dismutase, catalase, and peroxidase levels in erythrocytes and livers of different freshwater and marine fish species. Comp. Biochem. Physiol. B 1982, 73:361-365.
64. Yong J.I., Guang-hua L.U., Wang C.H., Zhang J. Biochemical responses of freshwater fish Carassius auratus to polycyclic aromatic hydrocarbons and pesticides. Water Sci. Engineer. 2012, 5:145-154.
65. Zorrilla García A.E. El envejecimiento y el estrés oxidativo. Rev. Cubana Invest. Biomed. 2002, 21:178-185.