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复方米非司酮对人早孕蜕膜组织雌孕激素受体的影响
引用本文:金力,沈维雄,孙志达,范光升,乌毓明,王寒正.复方米非司酮对人早孕蜕膜组织雌孕激素受体的影响[J].生殖与避孕,2000,20(4):202-208.
作者姓名:金力  沈维雄  孙志达  范光升  乌毓明  王寒正
作者单位:1. 中国医学科学院北京协和医科大学北京协和医院妇产科,北京,100730
2. 上海计划生育科学研究所分子生物学实验室,上海,200032
基金项目:本课题由上海计划生育科学研究所,国家计划生育药具重点实验室资助
摘    要:观察服用复方米非司酮片 (米非司酮 + AF-5 3)后早孕妇女蜕膜组织雌孕激素受体的变化。 6 0名孕 6~ 7周的妇女被随机分为 6组 ,A组 :对照组 ;B组 :米非司酮 40 mg/次 ;C组 :米非司酮 75 mg/次 ;D组 :复方米非司酮 1片 (米非司酮 2 0 mg+ AF-5 35 mg) ;E组 :复方米非司酮 1片 (米非司酮 30 mg+ AF-5 35 mg) ;F组 :复方米非司酮 1片 (米非司酮40 mg+ AF-5 35 mg)。以上各服药组 ,均为上述剂量每日 1次 ,连服 2日。服药 48h后手术终止妊娠 ,取蜕膜组织 ,放射性配体结合试验测定其胞浆、胞核雌、孕激素受体浓度。结果显示 :复方米非司酮各配伍组均显著降低孕激素受体 (PR) ,升高雌激素受体 (ER) ,改变 ER/PR,促进流产发生。 E组使胞浆雌激素受体 (Ec R)显著高于其它各用药组 ,可能有利于流产后雌激素尽快作用于 ER,促进内膜恢复。结论提示复方米非司酮中米非司酮与AF-5 3配伍具有协同作用 ,改变了雌孕激素受体比例 ,促进流产的发生 ,E组有利于子宫内膜的恢复

关 键 词:米非司酮  双炔失碳酯  雌激素受体  孕激素受体  蜕膜
修稿时间:1999-08-17

The Effect of Mifepristone Compound on Esrtrogen and Progestrone Receptors of Early Pregnancy in Decidua
JIN Li,SHEN Wei-xiong,SUN Zhi-da,FAN Guang-sheng,WU Yu-ming,WANG Han-zheng.The Effect of Mifepristone Compound on Esrtrogen and Progestrone Receptors of Early Pregnancy in Decidua[J].Reproduction and Contraception,2000,20(4):202-208.
Authors:JIN Li  SHEN Wei-xiong  SUN Zhi-da  FAN Guang-sheng  WU Yu-ming  WANG Han-zheng
Institution:JIN Li ;(Department of Obstetric and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, CAMS, Beijing, 100730);SHEN Wei-xiong ,SUN Zhi-da ;(Shanghai Institute of Planned Parenthood Research, Shanghai, 200032);FAN Guang-sheng ,WU Yu-ming ;(Department of Obstetric and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, CAMS, Beijing, 100730);WANG Han-zheng ;(Shanghai Institute of Planned Parenthood Research, Shanghai, 200032)
Abstract:WT5BZ] The effect of mifepristone compound on estrogen and progesterone receptors in decidua was studied. Sixty normal early pregnant volunteers(≤49 d)were randomly allocated into 6 groups,10 in each group. Group A:control group; Group B and Group C were administrated mifepristone 40 mg and 75 mg orally respectively, once per day, for two days; Group D(Group 4∶1): given mifepristone compound 1 tablet orally (mifepristone 20 mg+AF 53 5 mg)a day, for two days; Group E(Group 6∶1): given mifepristone compound 1 tablet(mifepristone 30 mg + AF 53 5 mg)a day, for two days; Group F(Group 8∶1): mifepristone compound 1 tablet(mifepristone 40 mg + AF 53 5 mg), at the same closeage above; concentration of ER and PR was measured by radio ligand assay in decidua tissue which were obstained after 48 h when mifepristone or mifepristone compound was administrated. Mifepristone compound in different doses significantly decreased the content of PR and increased ER and changed the balance of ER/PR. Among groups of mifepristone compound, Group E could also increased the concentration of EcR, which might be in favour of the endometrium recovery and shorten the bleeding days after abortion.
Keywords:Mifepristone  Anordrin  Decidua  Estrogen receptor  Progesterone receptor
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