Dynamics of estrogen biomarker responses in rainbow trout exposed to 17β-estradiol and 17α-ethinylestradiol

被引:56
作者
Thomas-Jones, E
Thorpe, K
Harrison, N
Thomas, G
Morris, C
Hutchinson, T
Woodhead, S
Tyler, C
机构
[1] Mol Light Technol Res, Cardiff CF14 5DL, S Glam, Wales
[2] AstraZeneca, Global Safety Hlth & Environm, Brixham Environm Lab, Brixham TQ5 8BA, Devon, England
[3] Univ Exeter, Sch Biol Sci, Exeter EX4 4PS, Devon, England
关键词
hybridization protection assay; endocrine disruption; rainbow trout; vitellogenin; gene expression;
D O I
10.1897/03-31
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We have investigated the response dynamics of the estrogen-dependent genes vitellogenin (VTG) and the vitelline envelope proteins (VEPs) as well as circulating VTG in immature female rainbow trout (Oncorhynchus mykiss) exposed to 17beta-pestradiol (E,) and 17alpha-ethinylestradiol (EE2) for periods of 7 and 14 d. Gene responses were quantified by measurement of messenger RNA (mRNA) in liver extracts using a chemiluminescent hybridization protection assay. Circulating VTG was measured by a homologous enzyme-linked immunosorbent assay. Exposure to both E-2 and EE2 induced concentration-dependent increases in all biomarkers. The data presented indicate that VEP genes may be more sensitive to estrogens than the VTG gene. The biomarker lowest-observed-effect concentrations ((LOEC)-L-biomarker) in the 14-d study with E2 were 14 ng/L (VTG protein, VTG mRNA, VEPbeta, and VEPgamma) or 4.8 ng/L (VEPalpha). The EE2 was 5- to 66-fold more potent depending on the biomarker studied. In the 7-d study, all biomarkers were elevated after 48-h exposure to E-2 with (LOECs)-L-biomarker of 30 ng/L (VTG protein, VTG mRNA, and VEPgamma) or 9.7 ng/L (VEPct and VEP). Vitellogenin mRNA was induced up to 1,000-fold above baseline, and this translated into an increase of approximately 50.000-fold in circulating VTG. In conclusion, all biomarkers responded to estrogen exposure at environmentally relevant concentrations.
引用
收藏
页码:3001 / 3008
页数:8
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