Coney P, Yoshimura Y, Hosoi Y, Bongiovanni A, Wallach E
Gynecol Obstet Invest. 1987;23(3):177-83. doi: 10.1159/000298859.
Two aromatase inhibitors, 4-hydroxyandrostenedione (4-OHA) and testololactone (Teslac), were tested to determine their effects on folliculogenesis, particularly ovarian histologic alterations, in the cycling rat. Adult, female Sprague-Dawley rats were treated with continuous infusion of both inhibitors at concentrations of 10(-8), 10(-4), and 10(-2) M for 30 days. The effect of the inhibitors on cultured granulosa cells harvested on proestrus was determined in vitro. The in vivo administration of each inhibitor induced significant reduction in ovarian-vein estradiol levels. Estradiol synthesis in cultured granulosa cells was inhibited by both aromatase inhibitors in a dose-dependent fashion. These observations indicate that 4-OHA and Teslac significantly inhibit basal estradiol synthesis in vivo and in vitro. This effect on estrogen synthesis was not reflected in alteration of the ovarian histology in the cycling rat.
对两种芳香化酶抑制剂,4-羟基雄烯二酮(4-OHA)和睾酮内酯(Teslac)进行了测试,以确定它们对成年雌性动情周期大鼠卵泡发生的影响,尤其是对卵巢组织学改变的影响。成年雌性斯普拉格-道利大鼠连续30天接受浓度为10^(-8)、10^(-4)和10^(-2) M的这两种抑制剂灌注。在体外测定了抑制剂对动情前期采集的培养颗粒细胞的作用。每种抑制剂的体内给药均导致卵巢静脉雌二醇水平显著降低。两种芳香化酶抑制剂均以剂量依赖性方式抑制培养颗粒细胞中的雌二醇合成。这些观察结果表明,4-OHA和Teslac在体内和体外均能显著抑制基础雌二醇合成。这种对雌激素合成的影响在动情周期大鼠的卵巢组织学改变中未得到体现。