Endosulfan in vitro toxicity in Atlantic salmon hepatocytes obtained from fish fed either fish oil or vegetable oil

Comparative Biochemistry and Physiology - C Toxicology and Pharmacology

Volumn 151, Issue 2, 2010, Pages 175-186

  Krøvel, Anne Vatland ^a   Søfteland, Liv ^a   Torstensen, Bente E ^a   Olsvik, Pål A ^a  

^a INSTITUTE OF MARINE RESEARCH   (Norway)

Author keywords

Atlantic salmon; Endosulfan; Exposure; Fatty acid composition; Feed; Hepatocytes; In vitro; Toxicity

Indexed keywords

ENDOSULFAN; ESTROGEN; FISH OIL; HEAT SHOCK PROTEIN 70; VEGETABLE OIL;

ARTICLE; ATLANTIC SALMON; BIOTRANSFORMATION; CELL CULTURE; CELL ISOLATION; CELL STRUCTURE; CYTOTOXICITY; FISH; GENE; IN VITRO STUDY; LIPID COMPOSITION; LIVER CELL; LIVER TOXICITY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; STEATOSIS; STRESS; SYSTEMATIC REVIEW;

SALMO SALAR;

EID: 72049131805     PISSN: 15320456     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpc.2009.10.003     Document Type: Article

References (63)

1. Ait-Aissa S., Porcher J., Arrigo A., and Lambre C. Activation of the hsp70 promoter by environmental inorganic and organic chemicals: relationships with cytotoxicity and lipophilicity. Toxicology 145 (2000) 147-157
2. Andersen H.R., Vinggaard A.M., Rasmussen T.H., Gjermandsen I.M., and Bonefeld-Jorgensen E.C. Effects of currently used pesticides in assays for estrogenicity, androgenicity, and aromatase activity in vitro. Toxicol. Appl. Pharmacol. 179 (2002) 1-12
3. Bajpayee M., Pandey A.K., Zaidi S., Musarrat J., Parmar D., Mathur N., Seth P.K., and Dhawan A. DNA damage and mutagenicity induced by endosulfan and its metabolites. Environ. Mol. Mutagen. 47 (2006) 682-692
4. Bakke-McKellep A.M., Froystad M.K., Lilleeng E., Dapra F., Refstie S., Krogdahl A., and Landsverk T. Response to soy: T-cell-like reactivity in the intestine of Atlantic salmon, Salmo salar L. J. Fish Dis. 30 (2007) 13-25
5. Berntssen M.H.G., Lundebye A.K., and Torstensen B.E. Reducing the levels of dioxins and dioxin-like PCBs in farmed Atlantic salmon by substitution of fish oil with vegetable oil in the feed. Aquac. Nutr. 11 (2005) 219-231
6. Berntssen M.H., Glover C.N., Robb D.H., Jakobsen J.V., and Petri D. Accumulation and elimination kinetics of dietary endosulfan in Atlantic salmon (Salmo salar). Aquat. Toxicol. 86 (2008) 104-111
7. Bradbury S.P., Carlson R.W., Henry T.R., Padilla S., and Cowden J. Toxic responses of the fish nervous system. In: Di Guilio R.T., and Hinton D.E. (Eds). The Toxicology of Fishes (2008), CRC Press, Taylor and Francis Group, Boca Raton, FL 417-456
8. Braunbeck T., and Appelbaum S. Ultrastructural alterations in the liver and intestine of carp Cyprinus carpio induced orally by ultra-low doses of endosulfan. Dis. Aquat. Org. 36 (1999) 183-200
9. Buhler D.R., Miranda C.L., Henderson M.C., Yang Y.H., Lee S.J., and Wang-Buhler J.L. Effects of 17beta-estradiol and testosterone on hepatic mRNA/protein levels and catalytic activities of CYP2M1, CYP2K1, and CYP3A27 in rainbow trout (Oncorhynchus mykiss). Toxicol. Appl. Pharmacol. 168 (2000) 91-101
10. Celius T., and Walther B.T. Differential sensitivity of zonagenesis and vitellogenesis in Atlantic salmon (Salmo salar L) to DDT pesticides. J. Exp. Zool. 281 (1998) 346-353
11. Coimbra A.M., Figueiredo-Fernandes A., and Reis-Henriques M.A. Nile tilapia (Oreochromis niloticus), liver morphology, CYP1A activity and thyroid hormones after Endosulfan dietary exposure. Pestic. Biochem. Physiol. 89 (2007) 230-236
12. Coumoul X., Diry M., Robillot C., and Barouki R. Differential regulation of cytochrome P450 1A1 and 1B1 by a combination of dioxin and pesticides in the breast tumor cell line MCF-7. Cancer Res. 61 (2001) 3942-3948
13. Coumoul X., Diry M., and Barouki R. PXR-dependent induction of human CYP3A4 gene expression by organochlorine pesticides. Biochem. Pharmacol. 64 (2002) 1513-1519
14. Dorval J., and Hontela A. Role of glutathione redox cycle and catalase in defense against oxidative stress induced by endosulfan in adrenocortical cells of rainbow trout (Oncorhynchus mykiss). Toxicol. Appl. Pharmacol. 192 (2003) 191-200
15. Dorval J., Leblond V.S., and Hontela A. Oxidative stress and loss of cortisol secretion in adrenocortical cells of rainbow trout (Oncorhynchus mykiss) exposed in vitro to endosulfan, an organochlorine pesticide. Aquat. Toxicol. 63 (2003) 229-241
16. Edmondson J.M., Armstrong L.S., and Martinez A.O. A rapid and simple MTT-based spectrophotometric assay for determining drug sensitivity in monolayer cultures. Methods Cell Sci. 11 (1988) 15-17
17. El-Zayadi A.R. Hepatic steatosis: a benign disease or a silent killer. World J. Gastroenterol. 14 (2008) 4120-4126
18. Espe M., Lemme A., Petrib A., and El-Mowafic A. Assessment of lysine requirement for maximal protein accretion in Atlantic salmon using plant protein diets. Aquaculture 263 (2007) 168-178
19. Fajas L., Debril M.B., and Auwerx J. Peroxisome proliferator-activated receptor-gamma: from adipogenesis to carcinogenesis. J. Mol. Endocrinol. 27 (2001) 1-9
20. Glover C.N., Petri D., Tollefsen K.E., Jorum N., Handy R.D., and Berntssen M.H. Assessing the sensitivity of Atlantic salmon (Salmo salar) to dietary endosulfan exposure using tissue biochemistry and histology. Aquat. Toxicol. 84 (2007) 346-355
21. Griffitt R.J., Chandler G.T., Greig T.W., and Quattro J.M. Cathepsin B and glutathione peroxidase show differing transcriptional responses in the grass shrimp, Palaemonetes pugio following exposure to three xenobiotics. Environ. Sci. Technol. 40 (2006) 3640-3645
22. Haasch M.L. Induction of anti-trout lauric acid hydroxylase immunoreactive proteins by peroxisome proliferators in bluegill and catfish. Mar. Environ. Res. 42 (1996) 287-291
23. Hutchinson T.H., Ankley G.T., Segner H., and Tyler C.R. Screening and testing for endocrine disruption in fish-biomarkers as "signposts," not "traffic lights," in risk assessment. Environ. Health Perspect. 114 Suppl 1 (2006) 106-114
24. Jackson J.E. A User's Guide to Principal Components (1991), John Wiley, New York
25. Jia Z., and Misra H.P. Reactive oxygen species in in vitro pesticide-induced neuronal cell (SH-SY5Y) cytotoxicity: role of NFkappaB and caspase-3. Free Radic. Biol. Med. 42 (2007) 288-298
26. Jordal A.E., Torstensen B.E., Tsoi S., Tocher D.R., Lall S.P., and Douglas S.E. Dietary rapeseed oil affects the expression of genes involved in hepatic lipid metabolism in Atlantic salmon (Salmo salar L.). J. Nutr. 135 (2005) 2355-2361
27. Jordal A.E.O., Lie O., and Torstensen B.E. Complete replacement of dietary fish oil with a vegetable oil blend affect liver lipid and plasma lipoprotein levels in Atlantic salmon (Salmo salar L.). Aquac. Nutr. 13 (2007) 114-130
28. Kannan K., Holcombe R.F., Jain S.K., Alvarez-Hernandez X., Chervenak R., Wolf R.E., and Glass J. Evidence for the induction of apoptosis by endosulfan in a human T-cell leukemic line. Mol. Cell Biochem. 205 (2000) 53-66
29. Keenan, J.J., 2003. Immunotixic Effects of Mixtures of Endosulfan and Permethrin Via Caspase Dependent Thymocyte Apoptosis. In: Department of Biomedical Sciences and Pathbiology, vol. Master of Science. Virginia Polytechnic Institute and State University, Blacksburg, Virginia, p. 51.
30. Krøvel A.V., Softeland L., Torstensen B., and Olsvik P.A. Transcriptional effects of PFOS in isolated hepatocytes from Atlantic salmon Salmo salar L. Comp. Biochem. Physiol., C Toxicol. Pharmacol. 148 (2008) 14-22
31. Kubista M., Sindelka R., Tichopad A., Bergkvist A., Lindh D., and Forootan A. The prime technique. G.I.T Lab. J. 9-10 (2007) 33-35
32. Leaver M.J., Bautista J.M., Bjornsson B.T., Jonsson E., Krey G., Tocher D.R., and Torstensen B.E. Towards fish lipid nutrigenomics: current state and prospects for fin-fish aquaculture. Reviews Fish. Sci. 16 (2008) 73-94
33. Lee S.M., Lee S.B., Park C.H., and Choi J. Expression of heat shock protein and hemoglobin genes in Chironomus tentans (Diptera, chironomidae) larvae exposed to various environmental pollutants: a potential biomarker of freshwater monitoring. Chemosphere 65 (2006) 1074-1081
34. Lie O., and Lambertsen G. Fatty-acid composition of glycerophospholipids in 7 tissues of cod (Gadus morhua), determined by combined high-performance liquid-chromatography and gas-chromatography. J. Chromatogr., Biomed. Appl. 565 (1991) 119-129
35. Lorenzatti E., Altahus R., Lajmanovich R., and Peltzer P. Residues of endosulfan in soy plants in Argentina croplands. Fresenius Environ. Bull. 13 (2004) 89-92
36. Morel Y., Mermod N., and Barouki R. An autoregulatory loop controlling CYP1A1 gene expression: role of H(2)O(2) and NFI. Mol. Cell. Biol. 19 (1999) 6825-6832
37. Naqvi S.M., and Vaishnavi C. Bioaccumulative potential and toxicity of endosulfan insecticide to non-target animals. Comp. Biochem. Physiol. C 105 (1993) 347-361
38. NRC. Nutrient Requirements of Fish (1993), NATIONAL ACADEMY PRESS, Washington, D.C
39. Oleksiak M.F., Wu S., Parker C., Qu W., Cox R., Zeldin D.C., and Stegeman J.J. Identification and regulation of a new vertebrate cytochrome P450 subfamily, the CYP2Ps, and functional characterization of CYP2P3, a conserved arachidonic acid epoxygenase/19-hydroxylase. Arch. Biochem. Biophys. 411 (2003) 223-234
40. Olsvik P.A., Lie K.K., Saele O., and Sanden M. Spatial transcription of CYP1A in fish liver. BMC Physiol. 7 (2007) 12
41. Pandey S., Ahmad I., Parvez S., Bin-Hafeez B., Haque R., and Raisuddin S. Effect of endosulfan on antioxidants of freshwater fish Channa punctatus Bloch: 1. Protection against lipid peroxidation in liver by copper preexposure. Arch. Environ. Contam. Toxicol. 41 (2001) 345-352
42. Panserat S., Kolditz C., Richard N., Plagnes-Juan E., Piumi F., Esquerre D., Medale F., Corraze G., and Kaushik S. Hepatic gene expression profiles in juvenile rainbow trout (Oncorhynchus mykiss) fed fishmeal or fish oil-free diets. Br. J. Nutr. 100 (2008) 953-967
43. Petri D., Glover C.N., Ylving S., Kolas K., Fremmersvik G., Waagbo R., and Berntssen M.H. Sensitivity of Atlantic salmon (Salmo salar) to dietary endosulfan as assessed by haematology, blood biochemistry, and growth parameters. Aquat. Toxicol. 80 (2006) 207-216
44. Prasad K.S.N., and Chhabra A. Organo-chlorine pesticide residues in animal feeds and fodders. Indian J. Anim. Sci. 71 (2001) 1178-1180
45. Rosen E.D., Sarraf P., Troy A.E., Bradwin G., Moore K., Milstone D.S., Spiegelman B.M., and Mortensen R.M. PPAR gamma is required for the differentiation of adipose tissue in vivo and in vitro. Mol. Cell 4 (1999) 611-617
46. Rotchell J.M., and Ostrander G.K. Molecular markers of endocrine disruption in aquatic organisms. J. Toxicol. Environ. Health, B. Crit. Rev. 6 (2003) 453-496
47. Rubio M.G., Medina A.R., Diaz A.M., and Canada M.J.A. Influence of harvesting method and washing on the presence of pesticide residues in olives and olive oil. J. Agric. Food Chem. 54 (2006) 8538-8544
48. Sagstad A., Sanden M., Haugland O., Hansen A.C., Olsvik P.A., and Hemre G.I. Evaluation of stress- and immune-response biomarkers in Atlantic salmon, Salmo salar L., fed different levels of genetically modified maize (Bt maize), compared with its near-isogenic parental line and a commercial suprex maize. J. Fish Dis. 30 (2007) 201-212
49. Schlenk D., Celander M., Gallagher E.P., George S., James M., Kullman S.W., van der Hurk P., and Willett K. Biotransformation in fishes. In: Di Guilio R.T., and Hinton D.E. (Eds). The Toxicology of Fishes (2008), CRC Press, Taylor and Francis Group, Boca Raton, FL 153-235
50. Schroeder A., Mueller O., Stocker S., Salowsky R., Leiber M., Gassmann M., Lightfoot S., Menzel W., Granzow M., and Ragg T. The RIN: an RNA integrity number for assigning integrity values to RNA measurements. BMC Mol. Biol. 7 (2006) 3
51. Selvakumar S., Geraldine P., Shanju S., and Jayakumar T. Stressor-specitic induction of heat shock protein 70 in the freshwater prawn Macrobrachium malcolmsonii (H. Milne Edwards) exposed to the pesticides endosulfan and carbaryl. Pestic. Biochem. Physiol. 82 (2005) 125-132
52. Sohn H.Y., Kwon C.S., Kwon G.S., Lee J.B., and Kim E. Induction of oxidative stress by endosulfan and protective effect of lipid-soluble antioxidants against endosulfan-induced oxidative damage. Toxicol. Lett. 151 (2004) 357-365
53. Soto A.M., Chung K.L., and Sonnenschein C. The pesticides endosulfan, toxaphene, and dieldrin have estrogenic effects on human estrogen-sensitive cells. Environ. Health Perspect. 102 (1994) 380-383
54. Stubhaug I., Froyland L., and Torstensen B.E. Beta-oxidation capacity of red and white muscle and liver in Atlantic salmon (Salmo salar L.)-effects of increasing dietary rapeseed oil and olive oil to replace capelin oil. Lipids 40 (2005) 39-47
55. Thibaut R., Debrauwer L., Perdu E., Goksoyr A., Cravedi J.P., and Arukwe A. Regio-specific hydroxylation of nonylphenol and the involvement of CYP2K- and CYP2M-like iso-enzymes in Atlantic salmon (Salmo salar). Aquat. Toxicol. 56 (2002) 177-190
56. Todorcevic M., Vegusdal A., Gjoen T., Sundvold H., Torstensen B.E., Kjaer M.A., and Ruyter B. Changes in fatty acids metabolism during differentiation of Atlantic salmon preadipocytes; effects of n-3 and n-9 fatty acids. Biochim. Biophys. Acta, Mol. Cell Biol. Lipids 1781 (2008) 326-335
57. Torstensen B.E., Froyland L., and Lie O. Replacing dietary fish oil with increasing levels of rapeseed oil and olive oil - effects on Atlantic salmon (Salmo salar L.) tissue and lipoprotein lipid composition and lipogenic enzyme activities. Aquac. Nutr. 10 (2004) 175-192
58. Torstensen B.E., Bell J.G., Rosenlund G., Henderson R.J., Graff I.E., Tocher D.R., Lie O., and Sargent J.R. Tailoring of Atlantic salmon (Salmo salar L.) flesh lipid composition and sensory quality by replacing fish oil with a vegetable oil blend. J. Agric. Food Chem. 53 (2005) 10166-10178
59. Torstensen B.E., Nanton D.A., Olsvik P.A., Sundvold H., and Stubhaug I. Gene expression of fatty acid binding proteins (FABPs), fatty acid transport proteins (cd36 and FATP) and β-oxidation related genes in Atlantic salmon (Salmo salar L.) fed fish oil or vegetable oil. Aquacult. Nutr. 15 (2009) 440-451
60. Wan M.T., Kuo J.N., Buday C., Schroeder G., Van Aggelen G., and Pasternak J. Toxicity of alpha-, beta-, (alpha + beta)-endosulfan and their formulated and degradation products to Daphnia magna, Hyalella azteca, Oncorhynchus mykiss, Oncorhynchus kisutch, and biological implications in streams. Environ. Toxicol. Chem. 24 (2005) 1146-1154
61. Wood A.W., Janz D.M., and Van Der Kraak G.J. Cell death: investigation and application in fish toxicology. In: Mommsen T.T., and Moon T.W. (Eds). Biochem. Mol. Biol. Fish. vol. 6 (2005), Elsevier, Amsterdam 303-328
62. Yamaki T., Tsu-ura Y., Watanabe K., Fukuda T., and Suzuki T. Acute and reversible fatty metamorphosis of cultured rat hepatocytes. Pathol. Int. 47 (1997) 103-111
63. Zhu S., King S.C., and Haasch M.L. Environmental induction of CYP1A-, CYP2M1- and CYP2K1-like proteins in tropical fish species by produced formation water on the northwest shelf of Australia. Mar. Environ. Res. 62 Suppl (2006) S322-S326