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RU 38,486对妊娠早期蜕膜和胎盘中孕酮及雌激素受体浓度的影响。

The effect of RU 38,486 on progesterone and oestrogen receptor concentrations in the decidua and placenta in early pregnancy.

作者信息

Hill N C, Rivera J, Lopez Bernal A, MacKenzie I Z

机构信息

Nuffield Department of Obstetrics & Gynaecology, University of Oxford, John Radcliffe Hospital, Headington, UK.

出版信息

Hum Reprod. 1990 May;5(4):464-7. doi: 10.1093/oxfordjournals.humrep.a137124.

DOI:10.1093/oxfordjournals.humrep.a137124
PMID:2362009
Abstract

Decidual and placental concentrations of progesterone and oestrogen receptors in 15 women having medical terminations of pregnancy with a combination of the anti-progesterone steroid RU 38,486 and prostaglandin E1 analogue have been compared with 10 matched controls undergoing surgical aspiration of pregnancy. In the patients treated with RU 38,486, the mean (SD) decidual cytosolic and total progesterone receptor concentrations of 4.3 (5.6) and 7.6 (7.1) fmol/microgram DNA respectively were significantly lower than the levels of 18.5 (14.4) and 22.3 (17.4) fmol/microgram DNA in the control patients. Progesterone receptor concentrations in the placenta were very low in both groups. No significant change in oestrogen receptor concentrations occurred in the decidua or placenta after treatment with RU 38,486. These data indicate that there may be down-regulation of decidual progesterone receptor concentrations following RU 38,486 treatment.

摘要

将15名使用抗孕酮类固醇RU 38,486和前列腺素E1类似物联合进行中期妊娠药物流产的女性的蜕膜和胎盘组织中孕酮和雌激素受体浓度,与10名接受手术吸宫流产的匹配对照者进行了比较。在接受RU 38,486治疗的患者中,蜕膜胞浆和总孕酮受体浓度平均(标准差)分别为4.3(5.6)和7.6(7.1)fmol/微克DNA,显著低于对照患者的18.5(14.4)和22.3(17.4)fmol/微克DNA水平。两组胎盘组织中的孕酮受体浓度都非常低。用RU 38,486治疗后,蜕膜或胎盘组织中的雌激素受体浓度没有显著变化。这些数据表明,RU 38,486治疗后蜕膜孕酮受体浓度可能会下调。

相似文献

1
The effect of RU 38,486 on progesterone and oestrogen receptor concentrations in the decidua and placenta in early pregnancy.RU 38,486对妊娠早期蜕膜和胎盘中孕酮及雌激素受体浓度的影响。
Hum Reprod. 1990 May;5(4):464-7. doi: 10.1093/oxfordjournals.humrep.a137124.
2
Early changes of affinity and binding sites of progesterone and oestrogen receptors in decidua exposed to RU 486.暴露于RU 486的蜕膜中孕酮和雌激素受体亲和力及结合位点的早期变化
Hum Reprod. 1992 Aug;7(7):934-9. doi: 10.1093/oxfordjournals.humrep.a137774.
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Estrogen and progesterone receptors in human decidua after RU486 treatment.RU486治疗后人蜕膜中的雌激素和孕激素受体
Fertil Steril. 1993 Jul;60(1):69-74. doi: 10.1016/s0015-0282(16)56038-5.
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P29, an oestrogen receptor-associated protein, is down-regulated by mifepristone in first trimester human placenta and decidua.P29是一种雌激素受体相关蛋白,在孕早期人胎盘和蜕膜中会被米非司酮下调。
Hum Reprod. 1991 Oct;6(9):1338-41. doi: 10.1093/oxfordjournals.humrep.a137536.
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Transplacental passage of mifepristone and its influence on maternal and fetal steroid concentrations in the second trimester of pregnancy.米非司酮的胎盘转运及其对妊娠中期母胎甾体激素浓度的影响。
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The effect of RU 486 on progesterone receptor in villous and extravillous trophoblast.RU 486对绒毛和绒毛外滋养层中孕酮受体的影响。
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The placental transfer of mifepristone (RU 486) during the second trimester and its influence upon maternal and fetal steroid concentrations.米非司酮(RU 486)在孕中期的胎盘转运及其对母体和胎儿甾体激素浓度的影响。
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The effect of RU486 on progesterone and oestrogen receptor concentration in human decidua on early pregnancy.RU486对人早孕蜕膜中孕酮和雌激素受体浓度的影响。
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Progesterone receptor antagonists and prostaglandins in human fertility regulation: a clinical review.孕酮受体拮抗剂与前列腺素在人类生育调节中的应用:临床综述
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Early pregnancy termination with antiprogestins: a comparative clinical study of RU 486 given in two dose regimens and Epostane.抗孕激素用于早期妊娠终止:两种剂量方案的RU 486与依普孕酮的比较临床研究
Fertil Steril. 1987 Oct;48(4):565-70. doi: 10.1016/s0015-0282(16)59465-5.

引用本文的文献

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Mifepristone. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential.米非司酮。对其药效学和药代动力学特性以及治疗潜力的综述。
Drugs. 1993 Mar;45(3):384-409. doi: 10.2165/00003495-199345030-00007.