Modulatory actions of the new antiprogestins ZK 98.299 and ZK 98.734 and of RU 486 on luteinizing hormone secretion and progesterone effects in pituitary gonadotrophs

Olaf Ortmann , Katja Hansemann , Rudolf Knuppen , Günter Emons
{"title":"Modulatory actions of the new antiprogestins ZK 98.299 and ZK 98.734 and of RU 486 on luteinizing hormone secretion and progesterone effects in pituitary gonadotrophs","authors":"Olaf Ortmann ,&nbsp;Katja Hansemann ,&nbsp;Rudolf Knuppen ,&nbsp;Günter Emons","doi":"10.1016/0022-4731(90)90084-6","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of the antiprogestins (APs) ZK 98.299, ZK 98.734 and RU 486 on GnRH-stimulated LH secretion and their antagonistic activity on progesterone (P) actions were investigated in cultured pituitary cells from adult female Wistar rats. P (100 nM) was able to exert a facilitatory effect on GnRH (1 nM)-induced LH secretion after short-term (4h) treatment of estradiol-primed (1 nM, 48 h) rat pituitary cells. When the APs (10 pM–10 μM) were introduced during the 4 h incubation period with P the facilitatory effect of P was totally abolished at concentrations &gt; 10 nM (ZK 98.299, ZK 98.734) and &gt; 1 nM (RU 486). Also the APs were shown to block the inhibitory action of P which occurs after long-term incubation of pituitary cells with this steroid. However at concentrations &gt; 10 nM (ZK 98.734, RU 486) and &gt; 100 nM (ZK 98.299) this antagonistic action of the APs was lost. To evaluate whether the APs have direct effects on GnRH-induced LH secretion in the absence of exogenous P pituitary cells cultivated for 48 h with or without 1 nM estradiol were incubated for 4 or 24 h with increasing concentrations of the APs (10 pM–10 μM). Four hour treatment of nonestradiol-primed cells with ZK 98.299 or ZK 98.734 was without any effect on the LH response to a 1 nM GnRH-stimulus. Only the highest concentration of RU 486 (10 μM) reduced the LH response. Twenty-four hour treatment of the cultures with the APs led to enhancement of GnRH-stimulated LH secretion by up to 113, 37 and 33% for ZK 98.734, ZK 98.299 and RU 486, respectively. When estradiol-primed cells were used for the same experiments we observed exclusively inhibitory effects on GnRH-induced LH secretion after 4 and 24 h treatment periods.</p><p>It is concluded that these new APs are potent inhibitors of P-actions, but also <em>per se</em> they induce diverse effects on GnRH-stimulated LH secretion in cultured rat pituitary cells which have to be taken into account.</p></div>","PeriodicalId":17138,"journal":{"name":"Journal of steroid biochemistry","volume":"36 5","pages":"Pages 431-437"},"PeriodicalIF":0.0000,"publicationDate":"1990-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0022-4731(90)90084-6","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of steroid biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0022473190900846","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

Abstract

The effects of the antiprogestins (APs) ZK 98.299, ZK 98.734 and RU 486 on GnRH-stimulated LH secretion and their antagonistic activity on progesterone (P) actions were investigated in cultured pituitary cells from adult female Wistar rats. P (100 nM) was able to exert a facilitatory effect on GnRH (1 nM)-induced LH secretion after short-term (4h) treatment of estradiol-primed (1 nM, 48 h) rat pituitary cells. When the APs (10 pM–10 μM) were introduced during the 4 h incubation period with P the facilitatory effect of P was totally abolished at concentrations > 10 nM (ZK 98.299, ZK 98.734) and > 1 nM (RU 486). Also the APs were shown to block the inhibitory action of P which occurs after long-term incubation of pituitary cells with this steroid. However at concentrations > 10 nM (ZK 98.734, RU 486) and > 100 nM (ZK 98.299) this antagonistic action of the APs was lost. To evaluate whether the APs have direct effects on GnRH-induced LH secretion in the absence of exogenous P pituitary cells cultivated for 48 h with or without 1 nM estradiol were incubated for 4 or 24 h with increasing concentrations of the APs (10 pM–10 μM). Four hour treatment of nonestradiol-primed cells with ZK 98.299 or ZK 98.734 was without any effect on the LH response to a 1 nM GnRH-stimulus. Only the highest concentration of RU 486 (10 μM) reduced the LH response. Twenty-four hour treatment of the cultures with the APs led to enhancement of GnRH-stimulated LH secretion by up to 113, 37 and 33% for ZK 98.734, ZK 98.299 and RU 486, respectively. When estradiol-primed cells were used for the same experiments we observed exclusively inhibitory effects on GnRH-induced LH secretion after 4 and 24 h treatment periods.

It is concluded that these new APs are potent inhibitors of P-actions, but also per se they induce diverse effects on GnRH-stimulated LH secretion in cultured rat pituitary cells which have to be taken into account.

新型抗孕激素ZK 98.299、ZK 98.734和ru486对垂体促性腺激素促黄体生成素分泌和孕酮作用的调节作用
本文研究了抗孕激素ZK 98.299、ZK 98.734和RU 486对gnrh刺激下黄体生成素分泌的影响及其对孕酮(P)的拮抗作用。经雌二醇诱导的大鼠垂体细胞(1 nM, 48 h)短期(4h)处理后,P (100 nM)能够对GnRH (1 nM)诱导的LH分泌产生促进作用。当ap (10 pM-10 μM)与P共孵育4 h时,P的促进作用在浓度为>时完全消失;10 nM (ZK 98.299, ZK 98.734)和>1 nM (RU 486)。此外,APs被证明可以阻断垂体细胞与这种类固醇长期孵育后P的抑制作用。然而在浓度>10 nM (ZK 98.734, RU 486)和>100 nM (ZK 98.299)时,ap的拮抗作用消失。为了评估在没有外源性P的情况下,APs是否对gnrh诱导的LH分泌有直接影响,在1 nM雌二醇或不加雌二醇的情况下,将垂体细胞培养48 h,并增加APs浓度(10 pM-10 μM),孵育4或24 h。用ZK 98.299或ZK 98.734对非雌二醇引发的细胞处理4小时,对LH对1 nM gnrh刺激的反应没有任何影响。只有最高浓度的RU 486 (10 μM)降低了LH响应。用APs处理24小时后,ZK 98.734、ZK 98.299和RU 486的gnrh刺激的LH分泌量分别增加了13%、37%和33%。当使用雌二醇诱导的细胞进行相同的实验时,我们观察到在处理4和24 h后,对gnrh诱导的LH分泌有抑制作用。由此得出结论,这些新的APs是p -作用的有效抑制剂,但它们本身也会对培养的大鼠垂体细胞中gnrh刺激的LH分泌产生不同的影响,这是必须考虑的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信