Department of Biology and Canadian Rivers Institute, University of Prince Edward Island, Charlottetown, PE, Canada, C1A 4P3.
Aquat Toxicol. 2010 Jun 10;98(2):148-56. doi: 10.1016/j.aquatox.2010.02.002. Epub 2010 Feb 12.
Previous studies have shown that mummichog (Fundulus heteroclitus; a lunar, asynchronous-spawning killifish of the western Atlantic) exposed to 17alpha-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; 0-270ng/L) for 14 days. Following exposure, gonadal tissue was removed and incubated for 24h 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 (ERalpha) 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.
先前的研究表明,暴露于 17α-乙炔基雌二醇(EE2)的花鳉(一种来自西大西洋的具月周期、异步产卵的食蚊鱼)表现出血浆生殖类固醇水平降低、性腺类固醇产生减少、血浆卵黄蛋白原增加、繁殖力降低和受精能力受损。本研究的目的是确定 EE2 抑制性腺类固醇生成和影响花鳉雌激素信号转导的潜在机制。成年复育鱼暴露于强合成雌激素乙炔雌二醇(EE2;0-270ng/L)14 天。暴露后,取出性腺组织并在含有类固醇生成刺激剂的条件下孵育 24 小时,包括 forskolin;25-OH 胆固醇;或孕烯醇酮。基础、 forskolin 刺激和孕烯醇酮刺激的 EE2 暴露雄性鱼的睾酮产生减少,表明在胆固醇动员到 P450 侧链裂解(P450scc)和/或 P450scc 将胆固醇转化为孕烯醇酮的位置以及下游对类固醇生成途径均有影响。与对照复育雄性和雌性相比,EE2 处理雄性的肝雌激素受体α(ERalpha)和卵黄蛋白原的转录水平增加,证实了雌激素反应。肝热休克蛋白 90(Hsp90),一种参与雌激素信号转导的伴侣分子,在 EE2 暴露时,在转录或蛋白水平均不受影响。然而,在雌性鱼的膜部分观察到更高水平的 Hsp90 提出了关于性别对 Hsp90 在雌激素信号转导中的作用的有趣问题。这些结果表明,EE2 可以改变类固醇生成途径中的特定部位的类固醇生成,并可以刺激肝雌激素信号转导,为花鳉对外源性雌激素的内分泌反应的分子机制提供了重要信息。