Taguchi M, Kubota T, Aso T
Department of Obstetrics and Gynecology, Faculty of Medicine, Tokyo Medical and Dental University, Japan.
Gynecol Obstet Invest. 1995;39(3):192-6. doi: 10.1159/000292407.
The direct effect of danazol on the DNA synthesis and ultrastructure of human cultured endometrial stromal cells was studied. The analysis of the [3H]thymidine incorporation in the endometrial stromal cells cultured for 10 days indicated that the DNA synthesis was inhibited in a dose-dependent manner by danazol and testosterone, but not by medroxyprogesterone. The effect of 10(-7) M of danazol was blocked by cyproterone acetate, but RU-486 did not show any influence. The observation of the ultrastructure of the cultured cells revealed that 10(-7) M of danazol increased cytoplasmic lysosomes; however, 10(-5) M of danazol destroyed cell organelles and cytoskeleton resulted from the cell death. These results indicated that the biological effects of danazol were mainly mediated by androgen receptors, and 10(-5) M of danazol exhibited the toxic effect on the endometrial stromal cells.
研究了达那唑对人培养子宫内膜基质细胞DNA合成及超微结构的直接影响。对培养10天的子宫内膜基质细胞中[3H]胸腺嘧啶核苷掺入情况的分析表明,达那唑和睾酮以剂量依赖方式抑制DNA合成,而甲羟孕酮则无此作用。10(-7)M达那唑的作用被醋酸环丙孕酮阻断,但RU-486无任何影响。对培养细胞超微结构的观察显示,10(-7)M达那唑可增加细胞质溶酶体;然而,10(-5)M达那唑导致细胞器破坏和细胞骨架解体,进而引起细胞死亡。这些结果表明,达那唑的生物学效应主要由雄激素受体介导,且10(-5)M达那唑对子宫内膜基质细胞具有毒性作用。