Progesterone receptor modulators and progesterone antagonists in women's health

被引:41
作者
Spitz, IM [1 ]
Chwalisz, K
机构
[1] Shaare Zedek Med Ctr, Hormone Res Inst, IL-91031 Jerusalem, Israel
[2] Populat Council, Ctr Biomed Res, New York, NY 10021 USA
[3] Jenapharm GmbH & Co KG, Jena, Germany
关键词
abortion; cervical dilatation; dysfunctional uterine bleeding; ectopic pregnancy; endometriosis; HRT; IVF; mifepristone; progesterone antagonists (PAs); progesterone receptor modulators (PRMs); uterine myoma;
D O I
10.1016/S0039-128X(00)00194-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both progesterone receptor modulators (PRMs) as well as purl progesterone antagonists (PAs) have numerous proven and potential therapeutic applications in female health care. Mifepristone, a PRM with only marginal agonistic activity, together with a prostaglandin can terminate pregnancies of less than 9 weeks duration; mifepristone is also used in the preparation of women at later gestational stages whose pregnancies are terminated with prostaglandins or surgery, Mifepristone causes expulsion of the uterine contents following intrauterine fetal death and promotes dilation of the non-pregnant primigravid uterus. It is also effective in the treatment of missed abortion. Together with methotrexate, mifepristone can be used in the medical treatment of ectopic pregnancy. Both PAs and PRMs display antiproliferative effects on the endometrium. Because of this, they have application in the treatment of endometriosis, an estrogen-dependent condition. They may also be utilized to reduce myoma size, acting as both a PA and antiproliferative agent. Unlike GnRH agonists, long-term use in endometriosis and myoma is not associated with loss of bone and hypoestrogenism. PRMs may also be useful in IVF programs to prevent a premature LH surge and to delay the emergence of the implantation window. Some PRMs have potential use as hormone replacement therapy in women during menopause or in those with dysfunctional uterine bleeding. (C) 2000 Published by Elsevier Science Inc.
引用
收藏
页码:807 / 815
页数:9
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