Habenicht U F, el Etreby M F
Research Laboratories of Schering AG, Berlin (West)/Bergkamen, Federal Republic of Germany.
Prostate. 1987;11(2):133-43. doi: 10.1002/pros.2990110205.
We examined whether the induction of estrogen-related hyperplastic changes in the prostate (ie, activation and stimulation of the stroma, especially of the smooth muscle) of castrated beagle dogs was reproducible. The effectiveness of the aromatase inhibitor 1-methyl-androsta-1, 4-diene-3, 17-dione (1-Methyl-ADD) in antagonizing such estrogen-related alterations was investigated in comparison with a combined treatment of 1-Methyl-ADD and the antiandrogen CPA. These studies have demonstrated the suitability of the androstenedione model for testing the efficacy of aromatase inhibitors. In addition, it has been demonstrated that an aromatase inhibitor in combination with an antiandrogen can synergically inhibit the glandular and stromal components of the prostate.
我们研究了在去势比格犬前列腺中诱导雌激素相关增生性变化(即激活和刺激基质,尤其是平滑肌)是否具有可重复性。与1-甲基雄甾-1,4-二烯-3,17-二酮(1-Methyl-ADD)和抗雄激素环丙孕酮醋酸酯(CPA)联合治疗相比,研究了芳香化酶抑制剂1-Methyl-ADD拮抗此类雌激素相关改变的有效性。这些研究证明了雄烯二酮模型在测试芳香化酶抑制剂疗效方面的适用性。此外,已经证明芳香化酶抑制剂与抗雄激素联合使用可协同抑制前列腺的腺体和基质成分。