Simulation study of natural UV-B radiation on Catla catla and its impact on physiology, oxidative stress, Hsp 70 and DNA fragmentation

Journal of Photochemistry and Photobiology B: Biology

Volumn 149, Issue 1, 2015, Pages 156-163

  Singh, Moirangthem Kameshwor ^a   Sharma, Jai Gopal ^b   Chakrabarti, Rina ^a  

^a UNIVERSITY OF DELHI   (India)

^b DELHI TECHNOLOGICAL UNIVERSITY   (India)

Author keywords

Carbonyl protein; Catla catla; DNA damage; Hsp 70; Superoxide dismutase; UV B

Indexed keywords

CARBONYL PROTEIN; DNA; HEAT SHOCK PROTEIN 70; NITRIC OXIDE SYNTHASE; PROTEIN; SUPEROXIDE DISMUTASE; THIOBARBITURIC ACID REACTIVE SUBSTANCE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; CATLA CATLA; COMET ASSAY; CONTROLLED STUDY; DNA FRAGMENTATION; FISH; LARVAL STAGE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RADIATION DOSE; ULTRAVIOLET B RADIATION; ADVERSE EFFECTS; ANIMAL; CYPRINIDAE; GROWTH, DEVELOPMENT AND AGING; LARVA; METABOLISM; PHYSIOLOGY; RADIATION RESPONSE; SURVIVAL ANALYSIS; ULTRAVIOLET RADIATION;

CATLA CATLA;

ANIMALS; CYPRINIDAE; DNA FRAGMENTATION; HSP70 HEAT-SHOCK PROTEINS; LARVA; OXIDATIVE STRESS; SURVIVAL ANALYSIS; ULTRAVIOLET RAYS;

EID: 84934998676     PISSN: 10111344     EISSN: 18732682     Source Type: Journal    
DOI: 10.1016/j.jphotobiol.2015.05.019     Document Type: Article

References (59)

1. A. A. Groff, J. Da Silva, E. A. Nunes, M. Ianistcki, T. N. Guecheva, A. M. De Oliveira, C. P. F. De Oliveira, A. L. Val, J. A. P. Henriques, UVA/UVB induced genotoxicty and lesion repair in Colossoma macropomum and Arapaima gigas Amazonian fish, J. Photochem. Photobiol. B 99 (2010) 93-99.
2. E. Sucré, F. Vidussi, B. Mostajir, G. Charmantier, C. Lorin-Nebel, Impact of ultraviolet-B radiation on planktonic fish larvae: alteration of the osmoregulatory function, Aquat. Toxicol. 109 (2012) 194-201.
3. A. Carrasco-Malio, M. Díaz, M. Mella, M. J. Montoya, A. Miranda, M. F. Landaeta, G. Sánchez, M. E. Hidalgo, Are the intertidal fish highly resistant to UV-B radiation? A study based on oxidative stress in Girella laevifrons (Kyphosidae), Ecotox. Environ. Saf. 100 (2014) 93-98.
4. D. P. Hader, E. W. Elbling, C. E. Williamson, R. C. Worrest, Effects of UV radiation on aquatic ecosystems and interactions with climate change, Photochem. Photobiol. Sci. 10 (2011) 242-260.
5. I. L. Jokinen, H. M. Salo, E. Markkula, K. Rikalainen, M. T. Arts, H. I. Browman, Additive effects of enhanced ambient ultraviolet B radiation and increased temperature on immune function, growth and physiological condition of juvenile (parr) Atlantic salmon, Salmo salar, Fish Shellfish Immunol. 30 (2011) 102-108.
6. M. K. Singh, J. G. Sharma, R. Chakrabarti, Impact of UV-B radiation on the physiology of freshwater carp Labeo rohita larvae and evaluation of UV-B protective properties of seeds of Achyranthes aspera and vitamin C, Agric. Res. 2 (2013) 166-171.
7. M. K. Singh, J. G. Sharma, R. Chakrabarti, Effect of UV-B radiation on the defence system of Labeo rohita (Actinopterygii: Cypriniformes: Cyprinidae) larvae and its modulation by seed of Devil's Horsewhip, Achyranthes aspera, Acta. Icthyol. Piscat. 43 (2013) 119-126.
8. H. I. Browman, C. Rodríguez, F. Béland, J. Cullen, R. Davis, J. Kowenberg, P. Kuhun, B. McArthur, J. Runge, J. St-Pierre, R. Vetter, Impact of ultraviolet radiation on marine crustacean zooplankton and ichthyoplankton: a synthesis of results from the estuary and Gulf of St. Lawrence, Canada, Mar. Ecol. Prog. Ser. 199 (2000) 293-311.
9. M. D. Lamare, J. Hoffman, Natural variation of carotenoids in the eggs and gonads of the echinoid genus, Strongylocentrotus: implications for their role in ultraviolet radiation photoprotection, J. Exp. Mar. Biol. Ecol. 312 (2004) 215-233.
10. B. Obermüller, U. Karsten, D. Abele, Response of oxidative stress parameters and sunscreening compounds in Arctic amphipods during experimental exposure to maximal natural UVB radiation, J. Exp. Mar. Biol. Ecol. 323 (2005) 100-117.
11. D. P. Häder, H. D. Kumar, R. C. Smith, R. C. Worrest, Effects of solar UV radiation on aquatic ecosystems and interactions with climate change, Photochem. Photobiol. Sci. 6 (2007) 267-285.
12. A. L. Val, C. A. Castro-Perez, V. M. F. Almeida-Val, UV an environmental challenge for fish of Amazon, in: S. Dee (Ed.), VI International Congress on Biology of Fishes, 2004, Manaus, Advance in Fish Biology, American Fisheries Society-Physiology Section 1, Vancouver, 2004, pp. 1-5.
13. H. U. Dahms, J. S. Lee, UV radiation in marine ectoderms: molecular effects and response, Aquat. Toxicol. 97 (2010) 3-14.
14. D. L. Mitchell, R. S. Nairn, D. A. Jhonston, M. Byrom, S. Kazianis, R. B. Walter, Decreased level of (6-4) photoproduct excision repair in hybrid fish of genus Xiphophorus, Photochem. Photobiol. 79 (2004) 447-452.
15. E. R. Vehniainen, K. Vahakangas, A. O. J. Oikari, UV-B exposure causes DNA damages and changes in protein expression in Northern pike (Esox lucius) post hatched embryo, Photochem. Photobiol. 88 (2012) 363-370.
16. J. Z. Sandrini, G. S. Trinade, L. E. M. Nery, L. F. Marins, Time-course expression of DNA repair-related genes in hepatocytes of zebrafish after UV-B exposure, Photochem. Photobiol. 85 (2009) 220-226.
17. S. Courdavault, C. Baudouin, M. Charveron, B. Canguilhem, A. Favier, J. Cadet, T. Douki, Repair of the three main types of bipyrimidine DNA photoproducts in human keratinocytes exposed to UVB and UVA radiations, DNA Repair 4 (2005) 836-844.
18. L. G. Schaumburg, G. L. Polettaa, A. Imhof, P. A. Siroski, Ultraviolet radiationinduced genotoxic effects in the broad-snouted caiman, Caiman latirostris, Mutat. Res. 700 (2010) 67-70.
19. L. Dalle-Donne, R. Rossi, D. Giustarini, A. Milzani, R. Colombo, Protein carbonyl groups as biomarkers of oxidative stress, Clin. Chim. Acta 329 (2003) 23-38.
20. R. J. Roberts, C. Agius, C. Saliba, P. Bossier, Y. Y. Sung, Heat shock proteins (chaperones) in fish and shellfish and their potential role in relation to fish health: a review, J. Fish Dis. 33 (2010) 789-801.
21. M. Yamashita, T. Yabu, N. Ojima, Stress protein HSP70 in fish, Aqua-BioScience Mono. 3 (2010) 111-141.
22. http://www.fao.org/fishery/culturedspecies/Catla-catla/en.
23. R. Bertoni, C. Callieri, Effects of UVB radiation on freshwater autotrophic and heterotrophic picoplankton in a subalpine lake, J. Plankton Res. 21 (1999) 1373-1388.
24. O. H. Lowry, N. J. Rosebrough, F. R. Farr, Protein measurement with the folin phenol reagent, J. Biol. Chem 193 (1951) 265-275.
25. A.-G. Lenz, U. Costabel, S. Shaltiel, R. L. Levine, Determination of carbonyl groups in oxidatively modified proteins by reduction with titrated sodium borohydride, Anal. Biochem. 177 (1989) 419-425.
26. H. Ohkawa, N. Ohishi, K. Yagi, Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction, Anal. Biochem. 95 (1979) 351-358.
27. D. U. Lee, Y. J. Kang, M. K. Park, Effects of 13-alkyl-substituted berberine alkaloids on the expression of COX-II, TNF-α, iNOS and IL-12 production in LPS stimulated macrophages, Life Sci. 73 (2003) 1401-1412.
28. P. Kakkar, B. Das, P. N. Viswanathan, A modified spectrophotometric assay of superoxide dismutase, J. Biochem. Biophys. 21 (1984) 130-131.
29. O. Osting, K. Johanson, Microelectrophoretic study of radiation induced DNA damages in individual mammalian cells, Biochem. Biophys. Res. Commun. 123 (1984) 291-298.
30. S. Chandna, Single-cell gel electrophoresis assay monitors precise kinetics of DNA fragmentation induced during programmed cell death, Cytometry Part A 61A (2004) 127-133.
31. D. C. Montgomery, Design and Analysis of Experiments, John Wiley, New York, USA, 1984.
32. J. G. Sharma, P. Mittal, R. Chakrabarti, Development of survivorship model for UV-B irradiated Catla catla larvae, Aquat. Ecol. 42 (2008) 17-23.
33. J. G. Sharma, R. Masuda, M. Tanaka, Ultrastructural study of skin and eye of UV-B irradiated ayu, Plecoglossus altivelius, J. Fish Biol. 67 (2005) 1646-1652.
34. J. G. Sharma, Y. V. Rao, S. Kumar, R. Chakrabarti, Impact of UV-B radiation on the digestive enzymes and immune system of larvae of Indian major carp Catla catla, Int. J. Radiat. Biol. 3 (2010) 181-186.
35. S. Karthi, R. Sankari, M. S. Shivakumar, Ultraviolet-B light induced oxidative stress: effects on antioxidant response of Spodoptera litura, J. Photochem. Photobiol. B 135 (2014) 1-6.
36. D. Abele, S. Puntarulo, Formation of reactive species and induction of antioxidant defence systems in polar and temperate marine invertebrates and fish, Comp. Biochem. Physiol. A 138 (2004) 405-415.
37. C. Barata, I. Lekumberri, M. Vila-Escale, N. Prat, C. Porte, Trace metal concentration, antioxidant enzyme activities and susceptibility to oxidative stress in the trichoptera larvae Hydropsyche exocellata from the Llobregat river basin (NE Spain), Aquat. Toxicol. 74 (2005) 3-19.
38. T. Hakozaki, D. Akira, T. Yoshii, S. Toyokuni, Visualization and characterization of UVB-induced reactive oxygen species in a human skin equivalent model, Arch. Dermatol. Res. 300 (2008) 51-56.
39. V. A. Terra, F. P. Souza-Neto, R. C. Pereira, T. N. X. Silva, A. C. Costa, R. C. Luiz, R. Cecchini, A. L. Cecchini, Time-dependent reactive species formation and oxidative stress damage in the skin after UVB irradiation, J. Photochem. Photobiol. B 109 (2012) 34-41.
40. E. Shacter, Protein oxidative damage, Methods Enzymol. 319 (2000) 428-436.
41. O. I. Kubrak, V. V. Husak, B. M. Rovenko, J. M. Storey, K. B. Storey, V. I. Lushchak, Cobalt-induced oxidative stress in brain, liver and kidney of goldfish Carassius auratus, Chemosphere 85 (2011) 983-989.
42. I. Dalle-Donne, A. Scaloni, D. Giustarini, E. Cavarra, G. Tell, G. Lungarella, R. Colombo, R. Rossi, A. Milzani, Proteins as biological markers of oxidative/nitrosative stress in diseases: the contribution of redox-proteomics, Mass Spectrom. Rev. 24 (2005) 55-99.
43. B. Friguet, L. I. Szweda, E. R. Stadtman, Susceptibility of glucose-6-phosphate dehydrogenase modified by 4-hydroxy-2-nonenal and metal-catalyzed oxidation to proteolysis by the multicatalytic protease, Arch. Biochem. Biophys. 311 (1994) 168-173.
44. V. I. Lushchak, T. V. Bagnyukova, V. V. Husak, L. I. Luzhna, O. V. Lushchak, K. B. Storey, Hyperoxia results in transient oxidative stress and an adaptive response by antioxidant enzymes in goldfish tissues, Int. J. Biochem. Cell B 37 (2005) 1670-1680.
45. E. M. Nazari, D. Ammar, A. Fabro De Bem, A. Litini, Y. M. M. Muller, S. Allodi, Effects of environmental and artificial UV-B on freshwater prawn Macrobrachium olfersi embyos, Aquat. Toxicol. 98 (2010) (2010) 25-33.
46. X. Y. Lu, R. S. S. Wu, UV induces reactive oxygen species, damages sperm, and impairs fertilisation in the sea urchin Anthocidaris crassispina, Mar. Biol. 148 (2005) 51-57.
47. L. Rochette, J. Lorin, M. Zeller, J. C. Guilland, L. Lorgis, Y. Cottin, C. Vergely, Nitric oxide synthase inhibition and oxidative stress in cardiovascular diseases: Possible therapeutic targets?, Pharmacol Therapeut. 140 (2013) 239-257.
48. G. Deviller, O. Palluel, C. Aliaume, H. Asanthi, W. Sanchez, M. A. Franco Nava, J. P. Blancheton, C. Casellas, Impact assessment of various rearing systems on fish health using multibiomarker response and metal accumulation, Ecotoxicol. Environ. Saf. 61 (2005) 89-97.
49. A. Sarkar, Biomarkers of marine pollution and bioremediation, Ecotoxicology 15 (2006) 331-332.
50. K. Asada, M. Takahashi, Production and scavenging of active oxygen in photosynthesis, in: D. J. Kyle, C. B. Osmond, C. J. Arntzen (Eds.), Photoinhibition, Elsevier, Amsterdam, 1987, pp. 228-287.
51. Z. W. Zhang, Z. Li, H.-W. Liang, L. Li, X.-Z. Luo, G.-W. Zou, Molecular cloning and differential expression patterns of Copper/Zinc superoxide dismutase and manganese superoxide dismutase in Hypophthalmichthys molitrix, Fish Shellfish Immunol. 30 (2011) 473-479.
52. M. P. Lesser, J. H. Farrel, C. W. Walker, Oxidative stress and p53 expression in the larvae of Atlantic cod (Gadus morhua) exposed to ultraviolet (290-400nm), J. Exp. Biol. 204 (2001) 157-164.
53. M. P. Lesser, T. M. Barry, Survivorship, development, and DNA damage in echinoderm embryos and larvae exposed to ultraviolet radiation (290-400 nm), J. Exp. Mar. Biol. Ecol. 292 (2003) 75-91.
54. C. Y. Li, J. S. Lee, Y. G. Ko, J. I. Kim, J. S. Seo, Suppression of heat shock protein-70 by ceramide in heat shock-induced HL-60 cell apoptosis, J. Biol. Chem. 275 (2000) 8872-8879.
55. D. D. Mosser, A. W. Caron, L. Bourget, A. B. Meriin, M. Y. Sherman, R. I. Morimoto, B. Massie, Heat shock protein 70 inhibits apoptosis downstream of cytochrome c release and upstream of caspase-3 activation, J. Biol. Chem. 275 (2000) 25665-25671.
56. D. D. Mosser, A. W. Caron, L. Bourget, C. Denis-Larose, B. Massie, The chaperone function of hsp70 is required for protection against stress-induced apoptosis, Mol. Cell Biol. 20 (2000) 7146-7159.
57. R. A. Krebs, M. E. Feder, Tissue-specific variation in Hsp70 expression and thermal damage in Drosophila melanogaster larvae, J. Exp. Biol. 200 (1997) 2007-2015.
58. J. A. Imlay, S. Linn, DNA damage and oxygen radical toxicity, Science 240 (1988) 1302-1309.
59. D. P. Valenzeno, J. P. Pooler, Photodynamic action, Bioscience 37 (1987) 270-276.