Effects of prolonged exposure to low pH on enzymatic and non-enzymatic antioxidants in Japanese Medaka (Oryzias latipes)

Science of the Total Environment

Volumn 568, Issue , 2016, Pages 26-32

  Ramírez Duarte, Wilson F ^a   Jin, Jiali ^a   Kurobe, Tomofumi ^a   Teh, Swee J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Acidification; Fish; Glutathione peroxidase; Oxidative stress; RT qPCR; Soft water

Indexed keywords

ACIDIFICATION; ANTIOXIDANTS; AQUATIC ECOSYSTEMS; FISH; OXIDATIVE STRESS; PEPTIDES; POLYMERASE CHAIN REACTION; TOXICITY;

ANTIOXIDANT MECHANISMS; ENZYMATIC AND NON-ENZYMATIC ANTIOXIDANTS; GLUTATHIONE CONCENTRATION; GLUTATHIONE PEROXIDASE; REACTIVE OXYGEN SPECIES; RT-QPCR; SOFT WATER; THIOBARBITURIC ACID REACTIVE SUBSTANCES;

PH EFFECTS;

ANTIOXIDANT; CATALASE; GLUTATHIONE; GLUTATHIONE PEROXIDASE; REACTIVE OXYGEN METABOLITE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; FISH PROTEIN;

ACIDIFICATION; ANTIOXIDANT; ATMOSPHERIC POLLUTION; ENZYME; FISH; OXIDATION; PH; POLYMERASE CHAIN REACTION;

ACIDIFICATION; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; FEMALE; GENE EXPRESSION; LARVA; LIPID PEROXIDATION; LONG TERM EXPOSURE; MALE; MORTALITY; NONHUMAN; ORYZIAS LATIPES; PH; PRIORITY JOURNAL; ANIMAL; GENETICS; METABOLISM; ORYZIAS; OXIDATIVE STRESS; TIME FACTOR; TOXICITY TESTING;

ORYZIAS LATIPES;

ANIMALS; ANTIOXIDANTS; FEMALE; FISH PROTEINS; GENE EXPRESSION; GLUTATHIONE; GLUTATHIONE PEROXIDASE; HYDROGEN-ION CONCENTRATION; MALE; ORYZIAS; OXIDATIVE STRESS; TIME FACTORS; TOXICITY TESTS, CHRONIC;

EID: 84973400131     PISSN: 00489697     EISSN: 18791026     Source Type: Journal    
DOI: 10.1016/j.scitotenv.2016.05.179     Document Type: Article

References (47)

1. Bagnyukova T.V., Vasylkiv O.Y., Storey K.B., Lushchak V.I. Catalase inhibition by amino triazole induces oxidative stress in goldfish brain. Brain Res. 2005, 1052:180-186.
2. Baines G.W. Blood pH effects in eight fishes from the teleostean family Scorpaenidae. Comp. Biochem. Physiol. A Physiol. 1975, 51:833-843.
3. Baker M.A., Cerniglia G.J., Zaman A. Microtiter plate assay for the measurement of glutathione and glutathione disulfide in large numbers of biological samples. Anal. Biochem. 1990, 190:360-365.
4. Barja de Quiroga G., Gil P., López-Torres M. Physiological significance of catalase and glutathione peroxidases, and in vivo peroxidation, in selected tissues of the toad Discoglossus pictus (Amphibia) during acclimation to normobaric hyperoxia. J. Comp. Physiol. B. 1988, 158:583-590.
5. Buckler D.R., Cleveland L., Little E.E., Brumbaugh W.G. Survival, sublethal responses, and tissue residues of Atlantic salmon exposed to acidic pH and aluminum. Aquat. Toxicol. 1995, 31:203-216.
6. Burton R.F. The dependence of normal arterial blood pH on sodium concentration in teleost fish. Comp. Biochem. Physiol. A Physiol. 1996, 114:111-116.
7. Carvalho C.S., Bernusso V.A., Fernandes M.N. Copper levels and changes in pH induce oxidative stress in the tissue of curimbata (Prochilodus lineatus). Aquat. Toxicol. 2015, 167:220-227.
8. Dangles O., Malmqvist B., Laudon H. Naturally acid freshwater ecosystems are diverse and functional: evidence from boreal streams. Oikos 2004, 104:149-155.
9. DeKoven D.L., Núñez J.M., Lester S.M., Conklin D.E., Marty G.D., Parker L.M., et al. A purified diet for medaka (Oryzias latipes): refining a fish model for toxicological research. Lab. Anim. Sci. 1992, 42:180-189.
10. Fernández-Díaz C., Kopecka J., Cañavate J.P., Sarasquete C., Solé M. Variations on development and stress defences in Solea senegalensis larvae fed on live and microencapsulated diets. Aquaculture 2006, 251:573-584.
11. Flohé L., Günzler W.A. Assays of glutathione peroxidase. Methods in Enzymology 1984, vol. 105:114-120. Academic Press.
12. Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine 2007, Oxford University Press, New York.
13. Hermes-Lima M. Oxygen in biology and biochemistry: role of free radicals. Functional Metabolism 2005, 319-368. John Wiley & Sons, Inc.
14. 2, in blood and water on breathing in rainbow trout, Salmo gairdneri. Respir. Physiol. 1975, 25:235-245.
15. Kinoshita M., Murata K., Naruse K., Tanaka M. Medaka: Biology, Management, and Experimental Protocols 2009, John Wiley & Sons, Ltd.
16. Lesser M.P. Oxidative stress in tropical marine ecosystems. Oxidative Stress in Aquatic Ecosystems 2011, 7-19. John Wiley & Sons, Ltd.
17. Lewis W.M., Weibezahn F.H., Saunders J.F., Hamilton S.K. The Orinoco River as an ecological system. Interciencia 1990, 15:346-357.
18. Li Z.-H., Zlabek V., Velisek J., Grabic R., Machova J., Kolarova J., et al. Acute toxicity of carbamazepine to juvenile rainbow trout (Oncorhynchus mykiss): effects on antioxidant responses, hematological parameters and hepatic EROD. Ecotoxicol. Environ. Saf. 2011, 74:319-327.
19. Livingstone D.R. Contaminant-stimulated reactive oxygen species production and oxidative damage in aquatic organisms. Mar. Pollut. Bull. 2001, 42:656-666.
20. 2. Pharmacol. Toxicol. 1990, 66:27-31.
21. López-Torres M., Pérez-Campo R., Barja de Quiroga G. Effect of natural ageing and antioxidant inhibition on liver antioxidant enzymes, glutathione system, peroxidation, and oxygen consumption in Rana perezi. J. Comp. Physiol. B. 1991, 160:655-661.
22. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the folin phenol reagent. J. Biol. Chem. 1951, 193:265-275.
23. Mai W.-j., Yan J.-1., Wang L., Zheng Y., Xin Y., Wang W.-n. Acute acidic exposure induces p53-mediated oxidative stress and DNA damage in tilapia (Oreochromis niloticus) blood cells. Aquat. Toxicol. 2010, 100:271-281.
24. Mattsoff L., Nikinmaa M. Effects of external acidification on the blood acid-base status and ion concentrations of lamprey. J. Exp. Biol. 1988, 136:351-361.
25. McWilliams P.G. An investigation of the loss of bound calcium from the gills of the brown trout, Salmo trutta, in acid media. Comp. Biochem. Physiol. A Physiol. 1983, 74:107-116.
26. McWilliams P.G., Potts W.T.W. The effects of pH and calcium concentrations on gill potentials in the brown trout, Salmo trutta. J. Comp. Physiol. 1978, 126:277-286.
27. Monserrat J., Letts R.E., Ferreira J.L.R., Ventura-Lima J., Amado L.L., Rocha A.M., et al. Biomarkers of oxidative stress: benefits and drawbacks for their application in biomonitoring of aquatic environments. Oxidative Stress in Aquatic Ecosystems 2011, 317-326. John Wiley & Sons, Ltd.
28. Newell A., Skjelkvåle B. Acidification trends in surface waters in the international program on acidification of rivers and lakes. Water Air Soil Pollut. 1997, 93:27-57.
29. Nikinmaa M., Weber R.E. Hypoxic acclimation in the lamprey, Lampetra fluviatilis: organismic and erythrocytic responses. J. Exp. Biol. 1984, 109:109-119.
30. Ohkawa H., Ohishi N., Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal. Biochem. 1979, 95:351-358.
31. Qu R., Feng M., Wang X., Qin L., Wang C., Wang Z., et al. Metal accumulation and oxidative stress biomarkers in liver of freshwater fish Carassius auratus following in vivo exposure to waterborne zinc under different pH values. Aquat. Toxicol. 2014, 150:9-16.
32. Reid S.D. Adaptation to and effects of acid water on the fish gill. Biochemistry and Molecular Biology of Fishes 1995, vol. 5:213-227. Elsevier. P.W. Hochachka, T.P. Mommsen (Eds.).
33. Remacle J., Lambert D., Raes M., Pigeolet E., Michiels C., Toussaint O. Importance of various antioxidant enzymes for cell stability. Confrontation between theoretical and experimental data. Biochem. J. 1992, 286:41-46.
34. Rivera-Rondón C.A., Zapata A.M., Pérez D., Morales Y., Ovalle H., Alvarez J.P. Limnological characterization of wetlands of the floodplain of the Orinoco River (Orinoco, Colombia). Acta Biol. Colomb. 2010, 15:145-166.
35. Rutledge R.G., Côté C. Mathematics of quantitative kinetic PCR and the application of standard curves. Nucleic Acids Res. 2003, 31.
36. Schmittgen T.D., Livak K.J. Analyzing real-time PCR data by the comparative CT method. Nat. Protoc. 2008, 3:1101-1108.
37. Shaw B.J., Al-Bairuty G., Handy R.D. Effects of waterborne copper nanoparticles and copper sulphate on rainbow trout, (Oncorhynchus mykiss): physiology and accumulation. Aquat. Toxicol. 2012, 116-117:90-101.
38. Sparling D.W. Acidic deposition: a review of biological effects. Handbook of Ecotoxicology 1995, 301-329. Lewis Publishers, Boca Raton, Florida. D.J. Hoffman, B.A. Rattner, G.A. Burton, J. Cairns (Eds.).
39. Stohs S.J., Bagchi D. Oxidative mechanisms in the toxicity of metal ions. Free Radic. Biol. Med. 1995, 18:321-336.
40. Tiedke J., Cubuk C., Burmester T. Environmental acidification triggers oxidative stress and enhances globin expression in zebrafish gills. Biochem. Biophys. Res. Commun. 2013, 441:624-629.
41. UNECE Convention on long-range transboundary air pollution. Concluded at Geneva (Switzerland) on 13 November 1979. Treaty Series 1983, 1302:217-224.
42. UNECE Protocol to the 1979 Convention on long-range transboundary air pollution to abate acidification, eutrophication and ground-level ozone. Concluded at Gothenburg (Sweden) on November 30, 1999. Treaty Series 2005, 2319:81-141.
43. Wada H., Shimada A., Fukamachi S., Naruse K., Shima A. Sex-linked inheritance of the lf locus in the Medaka fish (Oryzias latipes). Zool. Sci. 1998, 15:123-126.
44. Wu M., Khan I.A., Dasmahapatra A.K. Valproate-induced teratogenesis in Japanese rice fish (Oryzias latipes) embryogenesis. Comp. Biochem. Physiol., Part C: Toxicol. Pharmacol. 2012, 155:528-537.
45. Yada T., Ito F. Sexual difference in acid tolerance in medaka Oryzias latipes. Fish. Sci. 1998, 64:694-699.
46. Yosef N., Regev A. Impulse control: temporal dynamics in gene transcription. Cell 2011, 144:886-896.
47. Zhang Z., Hu J. Development and validation of endogenous reference genes for expression profiling of Medaka (Oryzias latipes) exposed to endocrine disrupting chemicals by quantitative real-time RT-PCR. Toxicol. Sci. 2007, 95:356-368.