Modulation of steroidogenesis and estrogen signalling in the estuarine killifish (Fundulus heteroclitus) exposed to ethinylestradiol

被引:45
|
作者
Hogan, Natacha S. [1 ,2 ]
Currie, Suzanne [3 ]
LeBlanc, Sacha [3 ]
Hewitt, L. Mark [4 ]
MacLatchy, Deborah L. [5 ,6 ]
机构
[1] Univ Prince Edward Isl, Dept Biol, Charlottetown, PE C1A 4P3, Canada
[2] Univ Prince Edward Isl, Canadian Rivers Inst, Charlottetown, PE C1A 4P3, Canada
[3] Mt Allison Univ, Dept Biol, Sackville, NB E4L 1G7, Canada
[4] Environm Canada, Aquat Ecosyst Protect Branch, Burlington, ON L7R 4A6, Canada
[5] Wilfrid Laurier Univ, Dept Biol, Waterloo, ON N2L 3C5, Canada
[6] Wilfrid Laurier Univ, Canadian Rivers Inst, Waterloo, ON N2L 3C5, Canada
关键词
Ethinylestradiol; Fundulus heteroclitus; Steroidogenesis; Estrogen receptor; Vitellogenin; Heat shock proteins; Endocrine disruption; ENDOCRINE-DISRUPTING CHEMICALS; KRAFT PULP-MILL; GOLDFISH CARASSIUS-AURATUS; VITELLOGENIN MESSENGER-RNA; HEAT-SHOCK-PROTEIN; RAINBOW-TROUT; BETA-SITOSTEROL; GENE-EXPRESSION; ENVIRONMENTAL ESTROGENS; STAR PROTEIN;
D O I
10.1016/j.aquatox.2010.02.002
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Previous studies have shown that mummichog (Fundulus heteroclitus; a lunar, asynchronous-spawning killifish of the western Atlantic) exposed to 17 alpha-ethynylestradiol (EE2) exhibit decreased plasma reproductive steroid levels, decreased gonadal steroid production, increased plasma vitellogenin, decreased fecundity and impaired fertilization. The objective of this study was to determine the potential mechanisms by which EE2 depresses gonadal steroidogenesis and influences estrogen signalling in the mummichog. Adult recrudesced fish were exposed to the potent synthetic estrogen, ethinylestradiol (EE2; 0-270 ng/L) for 14 days. Following exposure, gonadal tissue was removed and incubated for 24 h with stimulators of steroidogenesis, including forskolin; 25-OH cholesterol; or pregnenolone. Testosterone production was decreased in basal, forskolin-stimulated and pregnenolone-stimulated EE2-exposed males, indicating effects on the steroidogenic pathway both at and downstream of cholesterol mobilization to P450 side-chain cleavage (P450scc) and/or P450scc conversion of cholesterol to pregnenolone. Hepatic transcript levels of estrogen receptor alpha (ER alpha) and vitellogenin were increased in EE2-treated males compared to control recrudescing males and females confirming an estrogenic response. Hepatic heat shock protein 90 (Hsp90), a chaperoning molecule involved in estrogen signalling, was not affected by EE2 exposure at either the transcript or protein level. However, higher levels of Hsp90 observed in the membrane fractions of female fish raise interesting questions regarding the influence of gender on Hsp90's role in estrogen signalling. These results demonstrate that EE2 can alter steroid production at specific sites within the steroidogenic pathway and can stimulate hepatic estrogen signalling, providing important information regarding the molecular mechanisms underlying the endocrine response of the mummichog to exogenous estrogen. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:148 / 156
页数:9
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