Musich J R, Behrman S J, Menon K M
Am J Obstet Gynecol. 1981 May 1;140(1):62-9. doi: 10.1016/0002-9378(81)90258-1.
In order to study possible cellular estrogenic and/or antiestrogenic effects of danazol, immature female rats were treated with danazol (10 mg/kg/day) or propylene glycol (control) for 4 days (short-term study) and 14 days (long-term study). Estradiol receptor-binding assays were done on the cytosol fraction of the homogenized uterine tissue of each group. AT saturation levels of substrate, short-term danazol treatment was uterotropic and induced an increase in estradiol receptor concentration and binding (p less than 0.02). Long-term treatment, however, caused a marked decrease in estradiol receptor capacity (p less than 0.001). This disparity of the effect of danazol on estradiol receptors suggests a dose- or duration-dependent mechanism of action in the target tissue that may account for some of the clinical effects seen in patients receiving this drug.
为了研究达那唑可能的细胞雌激素和/或抗雌激素作用,对未成熟雌性大鼠用达那唑(10毫克/千克/天)或丙二醇(对照)处理4天(短期研究)和14天(长期研究)。对每组匀浆子宫组织的胞质溶胶部分进行雌二醇受体结合测定。在底物饱和水平下,短期达那唑处理具有促子宫生长作用,并诱导雌二醇受体浓度和结合增加(p<0.02)。然而,长期处理导致雌二醇受体容量显著降低(p<0.001)。达那唑对雌二醇受体作用的这种差异表明,在靶组织中存在剂量或持续时间依赖性作用机制,这可能解释了接受该药物的患者所观察到的一些临床效应。