Oxidative stress, DNA damage and antioxidant enzyme activities in the pacific white shrimp (Litopenaeus vannamei) when exposed to hypoxia and reoxygenation

Chemosphere

Volumn 144, Issue , 2016, Pages 234-240

  Li, Yuhu ^a,b   Wei, Lin ^a   Cao, Jiangrong ^c   Qiu, Liguo ^a   Jiang, Xiu ^a   Li, Ping ^a   Song, Qinqin ^a   Zhou, Hailong ^a   Han, Qian ^a   Diao, Xiaoping ^a  

^a HAINAN UNIVERSITY   (China)

^b Haikou Key Laboratory of Environment Toxicology   (China)

^c Hainan Provincial Health School   (China)

Author keywords

DNA damage; Hypoxia; Litopenaeus vannamei; Oxidative stress; Reoxygenation

Indexed keywords

BLOOD; DISSOLVED OXYGEN; DNA; ENZYMES; HISTOLOGY; OXIDATIVE STRESS; PLANTS (BOTANY); SHELLFISH;

ANTIOXIDANT ENZYME ACTIVITY; DISSOLVED OXYGEN LEVELS; DNA DAMAGES; HYPOXIA; HYPOXIA AND REOXYGENATION; LITOPENAEUS VANNAMEI; REOXYGENATION; SUPEROXIDE DISMUTASE ACTIVITIES;

TISSUE;

DISSOLVED OXYGEN; DNA; GLUTATHIONE PEROXIDASE; MALONALDEHYDE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE; OXYGEN;

CRUSTACEAN; DNA; ENZYME ACTIVITY; GENOTOXICITY; HYPOXIA; PHYSIOLOGY;

ACUTE DISEASE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BODY HEIGHT; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; ENVIRONMENTAL FACTOR; ENZYME ACTIVITY; GENOTOXICITY; GILL; HEMOLYMPH; HEPATOPANCREAS; HYPOXIA; LIPID PEROXIDATION; LITOPENAEUS VANNAMEI; METABOLIC RATE; MOLECULAR WEIGHT; NONHUMAN; OXIDATIVE STRESS; OXYGEN CONCENTRATION; REOXYGENATION; TISSUE LEVEL; TISSUE SPECIFICITY; UPREGULATION; ANIMAL; ANOXIA; COMET ASSAY; DOSE RESPONSE; DRUG EFFECTS; ENZYMOLOGY; GENETICS; METABOLISM; OXIDATION REDUCTION REACTION; PENAEIDAE; TIME FACTOR;

LITOPENAEUS VANNAMEI;

ANIMALS; ANOXIA; COMET ASSAY; DNA DAMAGE; DOSE-RESPONSE RELATIONSHIP, DRUG; GILLS; HEMOLYMPH; HEPATOPANCREAS; LIPID PEROXIDATION; MALONDIALDEHYDE; OXIDATION-REDUCTION; OXIDATIVE STRESS; OXYGEN; PENAEIDAE; SUPEROXIDE DISMUTASE; TIME FACTORS;

EID: 84953711839     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2015.08.051     Document Type: Article

References (40)

1. Abele D., Puntarulo S. Formation of reactive species and induction of antioxidant defence systems in polar and temperate marine invertebrates and fish. Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2004, 138:405-415.
2. 2+ and DNA damage in the white shrimp Litopenaeus vannamei. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2009, 149:581-586.
3. Coiro L.L., Poucher S.L., Miller D.C. Hypoxic effects on growth of Palaemonetes vulgaris larvae and other species: using constant exposure data to estimate cyclic exposure response. J. Exp. Mar. Biol. Ecol. 2000, 247:243-255.
4. Collins A.R. The comet assay for DNA damage and repair. Mol. Biotechnol. 2004, 26:249-261.
5. Collins A.R. Measuring oxidative damage to DNA and its repair with the comet assay. Biochim. Biophys. Acta Gen. Subj. 2014, 1840:794-800.
6. Fridovich I. Mitochondria: are they the seat of senescence?. Aging Cell 2004, 3:13-16.
7. Gray J.S., Wu R.S., Or Y.Y. Effects of hypoxia and organic enrichment on the coastal marine environment. Mar. Ecol. Prog. Ser. 2002, 238.
8. Halliwell B. Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol. 2006, 141:312-322.
9. Halliwell B., Gutteridge J. Free Radicals in Biology and Medicine 1985, Pergamon.
10. Haselmair A., Stachowitsch M., Zuschin M., Riedel B. Behaviour and mortality of benthic crustaceans in response to experimentally induced hypoxia and anoxia in situ. Mar. Ecol. Prog. Ser. 2010, 414:195-208.
11. Hegazi M.M., Attia Z.I., Ashour O.A. Oxidative stress and antioxidant enzymes in liver and white muscle of Nile tilapia juveniles in chronic ammonia exposure. Aquat. Toxicol. 2010, 99:118-125.
12. Hermes L.M., Zenteno S.T. Animal response to drastic changes in oxygen availability and physiological oxidative stress. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2002, 133:537-556.
13. Ji C., Wu H., Zhou M., Zhao J. Multiple biomarkers of biological effects induced by cadmium in clam Ruditapes philippinarum. Fish Shellfish Immunol. 2015, 44:430-435.
14. Jomova K., Valko M. Advances in metal-induced oxidative stress and human disease. Toxicology 2011, 283:65-87.
15. Lesser M.P. Oxidative Stress in Tropical Marine Ecosystems. Oxidative Stress in Aquatic Ecosystems 2012, 9-19. Blackwell Publishing Ltd.
16. Li C., Sun H., Chen A., Ning X., Wu H., Qin S., Xue Q., Zhao J. Identification and characterization of an intracellular Cu, Zn-superoxide dismutase (icCu/Zn-SOD) gene from clam Venerupis philippinarum. Fish Shellfish Immunol. 2010, 28:499-503.
17. Li C.Y., Jackson R.M. Reactive species mechanisms of cellular hypoxia-reoxygenation injury. Am. J. Physiol. Cell Physiol. 2002, 282:C227-C241.
18. Liu Y., Wang W.N., Wang A.L., Wang J.M., Sun R.Y. Effects of dietary vitamin E supplementation on antioxidant enzyme activities in Litopenaeus vannamei (Boone, 1931) exposed to acute salinity changes. Aquaculture 2007, 265:351-358.
19. Livingstone D.R. Contaminant-stimulated reactive oxygen species production and oxidative damage in aquatic organisms. Mar. Pollut. Bull. 2001, 42:656-666.
20. Lushchak V.I. Environmentally induced oxidative stress in aquatic animals. Aquat. Toxicol. 2011, 101:13-30.
21. Lushchak V.I., Lushchak L.P., Mota A.A., Hermes L.M. Oxidative stress and antioxidant defenses in goldfish Carassius auratus during anoxia and reoxygenation. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2001, 280:R100-R107.
22. McAllen R., Davenport J., Bredendieck K., Dunne D. Seasonal structuring of a benthic community exposed to regular hypoxic events. J. Exp. Mar. Biol. Ecol. 2009, 368:67-74.
23. Mohankumar K., Ramasamy P. White spot syndrome virus infection decreases the activity of antioxidant enzymes in Fenneropenaeus indicus. Virus Res. 2006, 115:69-75.
24. Muñoz M., Cedeño R., Rodríguez J., van der Knaap W.P., Mialhe E., Bachère E. Measurement of reactive oxygen intermediate production in haemocytes of the penaeid shrimp, Penaeus vannamei. Aquaculture 2000, 191:89-107.
25. Oakes K.D., Van Der Kraak G.J. Utility of the TBARS assay in detecting oxidative stress in white sucker (Catostomus commersoni) populations exposed to pulp mill effluent. Aquat. Toxicol. 2003, 63:447-463.
26. Pannunzio T.M., Storey K.B. Antioxidant defenses and lipid peroxidation during anoxia stress and aerobic recovery in the marine gastropod Littorina littorea. J. Exp. Mar. Biol. Ecol. 1998, 221:277-292.
27. Parrilla-Taylar D.P., Zenteno-Savín T. Antioxidant enzyme activities in Pacific white shrimp (Litopenaeus vannamei) in response to environmental hypoxia and reoxygenation. Aquaculture 2011, 318:379-383.
28. Qiu J., Wang W.N., Wang L.J., Liu Y.F., Wang A.L. Oxidative stress, DNA damage and osmolality in the Pacific white shrimp, Litopenaeus vannamei exposed to acute low temperature stress. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2011, 154:36-41.
29. Rabalais N.N., Turner R.E., Gupta B.S., Boesch D.F., Chapman P., Murrell M.C. Hypoxia in the northern Gulf of Mexico: does the science support the plan to reduce, mitigate, and control hypoxia?. Estuar. Coasts 2007, 30:753-772.
30. Robertson L., Bray W., Leung-Trujillo J., Lawrence A. Practical molt staging of Penaeus setiferus and Penaeus stylirostris. J. World Aquac. Soc. 1987, 18:180-185.
31. Singh N.P., McCoy M.T., Tice R.R., Schneider E.L. A simple technique for quantitation of low levels of DNA damage in individual cells. Exp. Cell Res. 1988, 175:184-191.
32. Storey K.B. Oxidative stress: animal adaptations in nature. Braz. J. Med. Biol. Res. 1996, 29:1715-1733.
33. Stramma L., Johnson G.C., Sprintall J., Mohrholz V. Expanding oxygen-minimum zones in the tropical oceans. Science 2008, 320:655-658.
34. Tyler R.M., Brady D.C., Targett T.E. Temporal and spatial dynamics of diel-cycling hypoxia in estuarine tributaries. Estuar. Coasts 2009, 32:123-145.
35. Wang W.N., Zhou J., Wang P., Tian T.T., Zheng Y., Liu Y., Mai W.J., Wang A.L. Oxidative stress, DNA damage and antioxidant enzyme gene expression in the Pacific white shrimp, Litopenaeus vannamei when exposed to acute pH stress. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2009, 150:428-435.
36. Wu R.S. Eutrophication, water borne pathogens and xenobiotic compounds: environmental risks and challenges. Mar. Pollut. Bull. 1999, 39:11-22.
37. Yang C., Liu S., Zhou S., Wu H., Yu J., Xia C. Allelochemical ethyl 2-methyl acetoacetate (EMA) induces oxidative damage and antioxidant responses in Phaeodactylum tricornutum. Pestic. Biochem. Physiol. 2011, 100:93-103.
38. Zenteno-Savín T., Saldierna R., Ahuejote-Sandoval M. Superoxide radical production in response to environmental hypoxia in cultured shrimp. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2006, 142:301-308.
39. Zhang L., Liu X., Chen L., You L., Pei D., Cong M., Zhao J., Li C., Liu D., Yu J., Wu H. Transcriptional regulation of selenium-dependent glutathione peroxidase from Venerupis philippinarum in response to pathogen and contaminants challenge. Fish Shellfish Immunol. 2011, 31:831-837.
40. Zhang L., Qiu L., Wu H., Liu X., You L., Pei D., Chen L., Wang Q., Zhao J. Expression profiles of seven glutathione S-transferase (GST) genes from Venerupis philippinarum exposed to heavy metals and benzo[a]pyrene. Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2012, 155:517-527.