Vitellogenic responses of 17β-estradiol and bisphenol A in male Chinese loach (Misgurnus anguillicaudatus)

Environmental Toxicology and Pharmacology

Volumn 24, Issue 2, 2007, Pages 155-159

  Lv, Xuefei ^a   Zhou, Qunfang ^a   Song, Maoyong ^a   Jiang, Guibin ^a   Shao, Jing ^a  

^a RESEARCH CENTER FOR ECO ENVIRONMENTAL SCIENCES   (China)

Author keywords

Bisphenol A; Chemical interaction; Chinese loach; Endocrine disruption; Estradiol; Experimental animal; Misgurnus anguillicaudatus; Vitellogenin

Indexed keywords

4,4' ISOPROPYLIDENEDIPHENOL; ESTRADIOL; VITELLOGENIN;

ARTICLE; CONTROLLED STUDY; DOSE RESPONSE; DOSE TIME EFFECT RELATION; ESTROGEN ACTIVITY; FISH; MALE; MISGURNUS ANGUILLICAUDATUS; NONHUMAN; PRIORITY JOURNAL; VITELLOGENESIS;

ANIMALIA; COBITIDAE; MISGURNUS ANGUILLICAUDATUS;

EID: 34447629208     PISSN: 13826689     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.etap.2007.04.007     Document Type: Article

References (21)

1. Brian J.V., Harris C.A., Scholze M., Backhaus T., Booy P., Lamoree M., Pojana G., Jonkers N., Runnalls T., Bonfà A., Marcomini A., and Sumpter J.P. Accurate prediction of the response of freshwater fish to a mixture of estrogenic chemicals. Environ. Health Perspect. 113 (2005) 721-728
2. Kanno S., Hirano S., and Kayama F. Effects of phytoestrogens and environmental estrogens on osteoblastic differentiation in MC3T3-E1 cells. Toxicology 196 (2004) 137-145
3. Larsen B.K., Bjørnstad A., Sundt R.C., Taban I.C., Pampanin D.M., and Andersen O.K. Comparison of protein expression in plasma from nonylphenol and bisphenol A-exposed Atlantic cod (Gadus morhua) and turbot (Scophthalmus maximus) by use of SELDI-TOF. Aquat. Toxicol. 78 (2006) S25-S33
4. Lindholst C., Pedersen K.L., and Pedersen S.N. Estrogenic response of bisphenol A in rainbow trout (Oncorhynchus mykiss). Aquat. Toxicol. 48 (2000) 87-94
5. Lutz I., Blödt S., and Kloas W. Regulation of estrogen receptors in primary cultured hepatocytes of the amphibian Xenopus laevis as estrogenic biomarker and its application in environmental monitoring. Comp. Biochem. Physiol. 141C (2005) 384-392
6. Lv X.F., Shao J., Song M.Y., Zhou Q.F., and Jiang G.B. Vitellogenic effects of 17β-estradiol in male Chinese loach (Misgurnus anguillicaudatus). Comp. Biochem. Physiol. 143C (2006) 127-133
7. Marin M.G., and Matozzo V. Vitellogenin induction as a biomarker of exposure to estrogenic compounds in aquatic environments. Mar. Pollut. Bull. 48 (2004) 835-839
8. Oehlmann J., Schulte-Oehlmann U., Bachmann J., Oetken M., Lutz I., Kloas W., and Ternes T.A. Bisphenol A induced superfeminization in the ramshorn snail Marisa cornuarietis (Gastropoda; Prosobranchia) at environmentally relevant concentrations. Environ. Health Perspect. 114 (2006) 127-133
9. Pait A.S., and Nelson J.O. Vitellogenesis in male Fundulus heteroclitus (killifish) induced by selected estrogenic compounds. Aquat. Toxicol. 64 (2003) 331-342
10. Panter G.H., Thompson R.S., and Sumpter J.P. Adverse reproductive effects in male fathead minnow (Pimephales promelas) exposed to environmentally relevant concentrations of the natural oestrogens, oestradiol and oestrone. Aquat. Toxicol. 42 (1998) 243-253
11. Payne J., Rajapakse N., Wilkins M., and Kortenkamp A. Predication and assessment of the effects of mixtures of four xenoestrogens. Environ. Health Perspect. 108 (2000) 983-987
12. Rajapakse N., Ong D., and Kortenkamp A. Defining the impact of weakly estrogenic chemicals on the action of steroidal estrogens. Toxicol. Sci. 60 (2001) 296-304
13. Rajapakse N., Silva E., and Kortenkamp A. Combing xenoestrogens at levels below individual no-observed-effect concentrations dramatically enhances steroid hormone action. Environ. Health Perspect. 110 (2002) 917-921
14. Routledge E.J., Sheahan D., Desbrow C., Brighty G.C., Waldock M., and Sumpter J.P. Identification of estrogenic chemicals in STW effluent. 2. In vivo responses in trout and roach. Environ. Sci. Technol. 32 (1998) 1559-1565
15. Shao J., Shi G.Q., Jin X.L., Song M.Y., Shi J.B., and Jiang G.B. Development and validation of an enzyme-linked immunosorbent assay for vitellogenin in Chinese loach (Misgurnus anguillicaudatus). Environ. Int. 31 (2005) 763-770
16. Shi G.Q., Shao J., Jiang G.B., Wang Q.X., Lu Y.Q., Liu J.F., and Liu J.M. Membrane chromatographic method for the rapid purification of vitellogenin from fish plasma. J. Chromatogr. B 785 (2003) 361-368
17. Silva E., Rajapakse N., and Kortenkamp A. Something from "nothing"-eight weak estrogenic chemicals combined at concentrations below NOECs produce significant mixture effects. Environ. Sci. Technol. 36 (2002) 1751-1756
18. Sumpter J.P., and Jobling S. Vitellogenesis as a biomarker for estrogenic contamination of the aquatic environment. Environ. Health Perspect. 103 (1995) 173-178
19. Thorpe K.L., Cummings R.I., Hutchinson T.H., Scholze M., Brighty G., Sumpter J.P., and Tyler C.R. Relative potencies and combination effects of steroids estrogens in fish. Environ. Sci. Technol. 37 (2003) 1142-1149
20. Van den Belt K., Verheyen R., and Witters H. Comparison of vitellogenin responses in zebrafish and rainbow trout following exposure to environmental estrogens. Ecotoxicol. Environ. Saf. 56 (2003) 271-281
21. Yamaguchi A., Ishibashi H., Kohra S., Arizono K., and Tominaga N. Short-term effects of endocrine-disrupting chemicals on the expression of estrogen-responsive genes in male medaka (Oryzias latipes). Aquat. Toxicol. 72 (2005) 239-249