Mechanisms of selenomethionine developmental toxicity and the impacts of combined hypersaline conditions on Japanese medaka (Oryzias latipes)

Environmental Science and Technology

Volumn 48, Issue 12, 2014, Pages 7062-7068

  Kupsco, Allison ^a   Schlenk, Daniel ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DEATH; CELL MEMBRANES; HATCHES; OXIDATIVE STRESS; PROTEINS; SELENIUM COMPOUNDS; WATER;

ACTIVATING TRANSCRIPTION FACTOR; DEVELOPMENTAL TOXICITY; ENDOPLASMIC RETICULUM; HYPERSALINE CONDITIONS; JAPANESE MEDAKA EMBRYOS; POST-FERTILIZATION; SELENOMETHIONINE (SEMET); UNFOLDED PROTEIN RESPONSE;

TOXICITY;

BINDING PROTEIN; FRESH WATER; HYPERSALINE; SELENOMETHIONINE; SODIUM CHLORIDE; UNCLASSIFIED DRUG;

APOPTOSIS; CONCENTRATION (COMPOSITION); EMBRYO; ENVIRONMENTAL STRESS; FISH; FRESHWATER ECOSYSTEM; HYPERSALINE ENVIRONMENT; LIPID; POLLUTANT SOURCE; POLLUTION EFFECT; POLLUTION EXPOSURE; SELENIUM; TRACE ELEMENT;

ADVERSE OUTCOME; APOPTOSIS; ARTICLE; DEVELOPMENTAL TOXICITY; EMBRYOTOXICITY; ENDOPLASMIC RETICULUM; ENVIRONMENTAL EXPOSURE; FERTILIZATION; GENE EXPRESSION; LIPID PEROXIDATION; NONHUMAN; NUCLEOTIDE SEQUENCE; ORYZIAS LATIPES; OXIDATIVE STRESS; TERATOGENESIS; UNFOLDED PROTEIN RESPONSE;

JAPAN;

ANIMALS; APOPTOSIS; EMBRYO, NONMAMMALIAN; FISH PROTEINS; GENE EXPRESSION REGULATION; LIPID PEROXIDATION; ORYZIAS; OXIDATIVE STRESS; SALINITY; SELENOMETHIONINE; TOXICITY TESTS; UNFOLDED PROTEIN RESPONSE;

EID: 84902581028     PISSN: 0013936X     EISSN: 15205851     Source Type: Journal    
DOI: 10.1021/es5019948     Document Type: Article

References (50)

1. Lemly, A. D. A teratogenic deformity index for evaluating impacts of selenium on fish populations Ecotoxicol. Environ. Saf. 1997, 37 (3) 259-66
2. Outridge, P. M.; Scheuhammer, A. M.; Fox, G. A.; Braune, B. M.; White, L. M.; Gregorich, L. J.; Keddy, C. An assessment of the potential hazards of environmental selenium for Canadian water birds Environ. Rev. 1999, 7 (2) 81-96
3. Muscatello, J. R.; Bennett, P. M.; Himbeault, K. T.; Belknap, A. M.; Janz, D. M. Larval Deformities associated with selenium accumulation in northern pike (Esox lucius) exposed to metal mining effluent Environ. Sci. Technol. 2006, 40 (20) 6506-6512
4. Presser, T. S.; Piper, D. Z.; Bird, K. J.; Skorupa, J. P.; Hamilton, S. J.; Detwiler, S. J.; Huebner, M. A. The phosphoria formation: A model for forecasting global selenium sources to the environment. In Handbook of Exploration and Environmental Geochemistry, Chapter 11; James, R. H., Ed.; Elsevier Science B.V., 2004; Vol. 8, pp 299-319.
5. Ramirez, P., Jr.; Rogers, B. P. Selenium in a Wyoming grassland community receiving wastewater from an in situ uranium mine Arch. Environ. Contam. Toxicol. 2002, 42 (4) 431-6
6. Wen, H.; Carignan, J. Reviews on atmospheric selenium: Emissions, speciation and fate Atmos. Environ. 2007, 41 (34) 7151-7165
7. Fan, T. W.; Teh, S. J.; Hinton, D. E.; Higashi, R. M. Selenium biotransformations into proteinaceous forms by foodweb organisms of selenium-laden drainage waters in California Aquat. Toxicol. 2002, 57, 65-84
8. Phibbs, J.; Franz, E.; Hauck, D.; Gallego, M.; Tse, J. J.; Pickering, I. J.; Liber, K.; Janz, D. M. Evaluating the trophic transfer of selenium in aquatic ecosystems using caged fish, X-ray absorption spectroscopy and stable isotope analysis Ecotoxicol. Environ. Saf. 2011, 74 (7) 1855-1863
9. Luoma, S. N.; Rainbow, P. S. Why is metal bioaccumulation so variable? Biodynamics as a unifying concept Environ. Sci. Technol. 2005, 39 (7) 1921-31
10. Lemly, A. D. Symptoms and implications of selenium toxicity in fish: The Belews Lake case example Aquat. Toxicol. 2002, 57, 39-49
11. USEPA. Draft Aquatic Life Water Quality Criteria for Selenium; Office of Water and Office of Science and Technology: Washington, DC, 2004; http://water.epa.gov/scitech/swguidance/standards/criteria/aqlife/selenium/ upload/complete-2.pdf.
12. Lavado, R.; Shi, D.; Schlenk, D. Effects of salinity on the toxicity and biotransformation of l -selenomethionine in Japanese medaka (Oryzias latipes) embryos: Mechanisms of oxidative stress Aquat. Toxicol. 2011, 108, 18-22
13. Enright, C.; Culberson, S. D., Salinity trends, variability, and control in the northern reach of the San Francisco Estuary. San Francisco Estuary Watershed Sci. 2010, 7 (2).
14. Palace, V. P.; Spallholz, J. E.; Holm, J.; Wautier, K.; Evans, R. E.; Baron, C. L., Metabolism of selenomethionine by rainbow trout (Oncorhynchus mykiss) embryos can generate oxidative stress. Ecotoxicol. Environ. Saf. 2004; 58, 17-21.
15. Misra, S.; Hamilton, C.; Niyogi, S. Induction of oxidative stress by selenomethionine in isolated hepatocytes of rainbow trout (Oncorhynchus mykiss) Toxicol. In Vitro 2012, 621-629
16. Miller, L. L.; Wang, F.; Palace, V. P.; Hontela, A. Effects of acute and subchronic exposures to waterborne selenite on the physiological stress response and oxidative stress indicators in juvenile rainbow trout Aquat. Toxicol. 2007, 83, 263-271
17. Hoffman, D. J.; Heinz, G. H.; LeCaptain, L. J.; Eisemann, J. D.; Pendleton, G. W. Toxicity and oxidative stress of different forms of organic selenium and dietary Arch. Environ. Contam. Toxicol. 1996, 31 (1) 120-7
18. Hetz, C. The unfolded protein response: Controlling cell fate decisions under ER stress and beyond Nat. Rev. Mol. Cell. Biol. 2012, 13 (2) 89-102
19. Kirchen, R. V.; West, W. R. The Japanese Medaka: Its Care and Development; Carolina Biological Supply Company,.
20. Schlenk, D.; Zubcov, N.; Zubcov, E. Effects of salinity on the uptake, biotransformation, and toxicity of dietary seleno-L-methionine to rainbow trout Toxicol. Sci. 2003, 75, 309-313
21. Farwell, A.; Nero, V.; Croft, M.; Bal, P.; Dixon, D. G. Modified Japanese medaka embryo-larval bioassay for rapid determination of developmental abnormalities Arch. Environ. Contam. Toxicol. 2006, 51 (4) 600-7
22. Zhao, S.; Fernald, R. D. Comprehensive algorithm for quantitative real-time polymerase chain reaction J. Comput. Biol. 2005, 12 (8) 1047-64
23. Schmittgen, T. D.; Livak, K. J. Analyzing real-time PCR data by the comparative C(T) method Nat. Protoc. 2008, 3 (6) 1101-8
24. Jentzsch, A. M.; Bachmann, H.; Furst, P.; Biesalski, H. K. Improved analysis of malondialdehyde in human body fluids Free Radical Biol. Med. 1996, 20 (2) 251-6
25. Inoue, K.; Takei, Y. Diverse adaptability in oryzias species to high environmental salinity Zool. Sci. 2002, 19 (7) 727-734
26. Chen, G. P.; Ziegler, D. M. Liver microsome and flavin-containing monooxygenase catalyzed oxidation of organic selenium compounds Arch. Biochem. Biophys. 1994, 312, 566-72
27. Schlenk, D.; Peters, L. D.; Livingstone, D. R. Correlation [corrected] of salinity with flavin-containing monooxygenase activity but not cytochrome P450 activity in the euryhaline fish (Platichthys flesus) Biochem. Pharmacol. 1996, 52, 815-8
28. El-Alfy, A.; Larsen, B.; Schlenk, D. Effect of cortisol and urea on flavin monooxygenase activity and expression in rainbow trout, Oncorhynchus mykiss Mar. Environ. Res. 2002, 54, 275-8
29. Spallholz, J. E.; Palace, V. P.; Reid, T. W. Methioninase and selenomethionine but not Se-methylselenocysteine generate methylselenol and superoxide in an in vitro chemiluminescent assay: Implications for the nutritional carcinostatic activity of selenoamino acids Biochem. Pharmacol. 2004, 67 (3) 547-54
30. Wang, Z.; Jiang, C.; Lü, J. Induction of caspase-mediated apoptosis and cell-cycle G1 arrest by selenium metabolite methylselenol Mol. Carcinogen. 2002, 34 (3) 113-120
31. Hackett, C.; Linley-Adams, M.; Lloyd, B.; Walker, V. Plasma malondialdehyde: A poor measure of in vivo lipid peroxidation Clin. Chem. 1988, 34 (1) 208
32. Wu, M.; Shariat-Madar, B.; Haron, M. H.; Khan, I. A.; Dasmahapatra, A. K. Ethanol-induced attenuation of oxidative stress is unable to alter mRNA expression pattern of catalase, glutathione reductase, glutathione-S-transferase (GST1A), and superoxide dismutase (SOD3) enzymes in Japanese rice fish (Oryzias latipes) embryogenesis Comp. Biochem. Physiol., C: Comp. Pharmacol. 2011, 153 (1) 159-67
33. Wu, Y.; Zhou, Q. Dose- and time-related changes in aerobic metabolism, chorionic disruption, and oxidative stress in embryonic medaka (Oryzias latipes): Underlying mechanisms for silver nanoparticle developmental toxicity Aquat. Toxicol. 2012, 124-125, 238-46
34. Wu, Y.; Zhang, H.; Dong, Y.; Park, Y. M.; Ip, C. Endoplasmic reticulum stress signal mediators are targets of selenium action Cancer. Res. 2005, 65 (19) 9073-9
35. Cullinan, S. B.; Diehl, J. A. Coordination of ER and oxidative stress signaling: The PERK/Nrf2 signaling pathway Int. J. Biochem. Cell Biol. 2006, 38 (3) 317-332
36. Nair, S.; Xu, C.; Shen, G.; Hebbar, V.; Gopalakrishnan, A.; Hu, R.; Jain, M. R.; Liew, C.; Chan, J. Y.; Kong, A. N. Toxicogenomics of endoplasmic reticulum stress inducer tunicamycin in the small intestine and liver of Nrf2 knockout and C57BL/6J mice Toxicol. Lett. 2007, 168, 21-39
37. Cribb, A. E.; Peyrou, M.; Muruganandan, S.; Schneider, L. The endoplasmic reticulum in xenobiotic toxicity Drug. Metab. Rev. 2005, 37, 405-442
38. DuRose, J. B.; Tam, A. B.; Niwa, M. Intrinsic capacities of molecular sensors of the unfolded protein response to sense alternate forms of endoplasmic reticulum stress Mol. Biol. Cell 2006, 17 (7) 3095-107
39. Cornejo, V. H.; Pihan, P.; Vidal, R. L.; Hetz, C. Role of the unfolded protein response in organ physiology: Lessons from mouse models IUBMB Life 2013, 65 (12) 962-75
40. Reimold, A. M.; Iwakoshi, N. N.; Manis, J.; Vallabhajosyula, P.; Szomolanyi-Tsuda, E.; Gravallese, E. M.; Friend, D.; Grusby, M. J.; Alt, F.; Glimcher, L. H. Plasma cell differentiation requires the transcription factor XBP-1 Nature 2001, 412 (6844) 300-7
41. Reimold, A. M.; Etkin, A.; Clauss, I.; Perkins, A.; Friend, D. S.; Zhang, J.; Horton, H. F.; Scott, A.; Orkin, S. H.; Byrne, M. C.; Grusby, M. J.; Glimcher, L. H. An essential role in liver development for transcription factor XBP-1 Genes Dev. 2000, 14 (2) 152-7
42. Han, X.; Zhou, J.; Zhang, P.; Song, F.; Jiang, R.; Li, M.; Xia, F.; Guo, F. J. IRE1alpha dissociates with BiP and inhibits ER stress-mediated apoptosis in cartilage development Cell. Signalling 2013, 25 (11) 2136-46
43. Sha, H.; He, Y.; Chen, H.; Wang, C.; Zenno, A.; Shi, H.; Yang, X.; Zhang, X.; Qi, L. The IRE1alpha-XBP1 pathway of the unfolded protein response is required for adipogenesis Cell. Metab. 2009, 9 (6) 556-64
44. Saito, A.; Ochiai, K.; Kondo, S.; Tsumagari, K.; Murakami, T.; Cavener, D. R.; Imaizumi, K. Endoplasmic reticulum stress response mediated by the PERK-eIF2(alpha)-ATF4 pathway is involved in osteoblast differentiation induced by BMP2 J. Biol. Chem. 2011, 286 (6) 4809-18
45. Weng, W. C.; Lee, W. T.; Hsu, W. M.; Chang, B. E.; Lee, H. Role of glucose-regulated Protein 78 in embryonic development and neurological disorders J. Formosan Med. Assoc. 2011, 110 (7) 428-37
46. Ishikawa, T.; Taniguchi, Y.; Okada, T.; Takeda, S.; Mori, K. Vertebrate unfolded protein response: Mammalian signaling pathways are conserved in Medaka fish Cell. Struct. Funct. 2011, 36 (2) 247-59
47. Ishikawa, T.; Okada, T.; Ishikawa-Fujiwara, T.; Todo, T.; Kamei, Y.; Shigenobu, S.; Tanaka, M.; Saito, T. L.; Yoshimura, J.; Morishita, S.; Toyoda, A.; Sakaki, Y.; Taniguchi, Y.; Takeda, S.; Mori, K. ATF6alpha/beta-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish Mol. Biol. Cell 2013, 24 (9) 1387-95
48. Benbrook, D. M.; Long, A. Integration of autophagy, proteasomal degradation, unfolded protein response and apoptosis Exp. Oncol. 2012, 34 (3) 286-97
49. Iijima, N.; Yokoyama, T. Apoptosis in the medaka embryo in the early developmental stage Acta Histochem. Cytochem. 2007, 40 (1) 1-7
50. Nijhawan, D.; Honarpour, N.; Wang, X. Apoptosis in neural development and disease Annu. Rev. Neurosci. 2000, 23, 73-87