Gschwendt M
Biochim Biophys Acta. 1975 Aug 13;399(2):395-402.
Nafoxidine and CI-628, two well known antiestrogenic compounds, reduce the stimulating effect of estradiol on the estrogen-binding capacity of the liver chromatin from roosters. In vitro both antiestrogens compete with [3H]estradiol for the binding sites on the liver chromatin. They inhibit the estrogen-induced synthesis of egg yolk proteins (vitellogenin) and fail to induce this estrogen-specific protein synthesis by themselves. They show the ability, however, to increase the estrogen-binding sites on the liver chromatin to some extent.
萘福昔定和CI-628这两种著名的抗雌激素化合物,可降低雌二醇对公鸡肝脏染色质雌激素结合能力的刺激作用。在体外,这两种抗雌激素均与[3H]雌二醇竞争肝脏染色质上的结合位点。它们抑制雌激素诱导的卵黄蛋白(卵黄生成素)合成,且自身无法诱导这种雌激素特异性蛋白合成。然而,它们在一定程度上显示出增加肝脏染色质上雌激素结合位点的能力。