School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1, Asahidai, Tatsunokuchi, Ishikawa 923-1292, Japan.
Environ Toxicol Pharmacol. 2004 May;17(1):29-33. doi: 10.1016/j.etap.2004.02.002.
The effects of oral administration of tamoxifen, 17α-ethynylestradiol (EE2), flutamide, and methyltestosterone (MT), on plasma vitellogenin levels of male and female medaka were investigated. Medaka were fed diets containing different concentrations of these chemicals for 7 days, and these plasma vitellogenin levels were measured. Tamoxifen increased significantly the vitellogenin levels in male, but inhibited the normal vitellogenin induction in female in the high concentration groups. EE2 increased significantly vitellogenin levels in both sexes. Flutamide increased significantly the vitellogenin levels in female, but gave no effects on male. MT inhibited the normal vitellogenin induction in female, but increased slightly vitellogenin levels in male without a clear tendency. Administration of tamoxifen, EE2, flutamide, and MT showed the different pattern in vitellogenin levels in both sexes.
研究了口服他莫昔芬、17α-乙炔基雌二醇(EE2)、氟他胺和甲基睾丸素(MT)对雄性和雌性半滑舌鳎血浆卵黄蛋白原水平的影响。半滑舌鳎喂食含有不同浓度这些化学物质的饮食 7 天,并测量这些血浆卵黄蛋白原水平。他莫昔芬显著增加了雄性的卵黄蛋白原水平,但在高浓度组中抑制了雌性的正常卵黄蛋白原诱导。EE2 显著增加了两性的卵黄蛋白原水平。氟他胺显著增加了雌性的卵黄蛋白原水平,但对雄性没有影响。MT 抑制了雌性的正常卵黄蛋白原诱导,但略微增加了雄性的卵黄蛋白原水平,没有明显的趋势。他莫昔芬、EE2、氟他胺和 MT 的给药在两性的卵黄蛋白原水平上表现出不同的模式。