Inhibition of human placental progesterone synthesis by danazol in vivo.

T Rabe, L Kiesel, C Franke, B Runnebaum, R Mösch, N Nobakht
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Abstract

In vivo, a single dose of 1000 mg danazol was given orally to pregnant volunteers (n = 8) prior to a therapeutic abortion (8th-12th week of gestation). Changes in serum progesterone and estradiol were evaluated both by analysis of percentage values related to initial concentrations or statistically by a Kruskal-Wallis test comparing absolute steroid concentrations. Following treatment (n = 8), a significant decrease in mean plasma progesterone of about 20% was observed within 2-4 hours; progesterone levels varied between 80-120% during 24 hours in controls (n = 10); individual serum estradiol decreased up to 30% of control values 2 hours after danazol application. Changes in estradiol in controls versus tests were not statistically significant (p less than 0.05) when absolute estradiol concentrations were compared. Only a slight (10-20%) decrease in mean serum DHAS was found between 2 to 6 hours following danazol treatment. This study demonstrates the inhibitory activity of danazol on the human maternal and fetal steroidogenesis in vivo. The possible sites of action of danazol are discussed.

达那唑对人胎盘孕酮合成的体内抑制作用。
在体内,怀孕志愿者(n = 8)在治疗性流产(妊娠8 -12周)前口服单剂量1000mg丹那唑。通过分析与初始浓度相关的百分比值或通过比较绝对类固醇浓度的Kruskal-Wallis试验进行统计分析,评估血清孕酮和雌二醇的变化。治疗后(n = 8),在2-4小时内观察到平均血浆孕酮显著下降约20%;对照组24小时内孕酮水平在80-120%之间变化(n = 10);个体血清雌二醇在应用达那唑2小时后下降到控制值的30%。当比较绝对雌二醇浓度时,对照组与试验组雌二醇的变化无统计学意义(p < 0.05)。在那那唑治疗后2至6小时内,平均血清DHAS仅轻微(10-20%)下降。本研究证实了那那唑对人母体和胎儿体内类固醇生成的抑制作用。讨论了那那唑可能的作用部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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