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化合物CDRI-85/287的抗雌激素活性持续时间:一种新型口服活性非甾体抗着床剂。

Duration of antiestrogenecity of compound CDRI-85/287: a new orally active nonsteroidal antiimplantation agent.

作者信息

Sreenivasulu S, Singh M M, Dwivedi A, Setty B S, Kamboj V P

机构信息

Division of Endocrinology, Central Drug Research Institute, Lucknow, India.

出版信息

Indian J Exp Biol. 1992 Nov;30(11):968-71.

PMID:1293041
Abstract

Duration of antiestrogenic and antiimplantation action of CDRI-85/287, (2-(4-(2-N-piperidino)ethoxy phenyl)-3-phenyl(2H)benzo(2)pyran), was studied in rat. Pretreatment of ovariectomized immature rats with this compound caused translocation of cytoplasmic estrogen receptor (ER) to the nucleus and a marked depletion of cytoplasmic ER pool resulting in a nonresponsive state of the uterus to subsequent estrogen administration until day 4. While in rats pretreated with estradiol, increased cytoplasmic ER level made the uterus responsive to a second injection of estrogen. In the delayed implantation model, 85/287 pretreated rats were given estrone on days 4, 5 or 6 post-antiestrogen treatment. No implantations were observed after estrone administration on day 4, but were present when estrone was given on days 5 or 6. Summation of these results suggests the duration of action of 85/287 to be 3-4 days in rat.

摘要

在大鼠中研究了CDRI-85/287(2-(4-(2-氮杂环己烷基)乙氧基苯基)-3-苯基(2H)苯并(2)吡喃)的抗雌激素和抗着床作用持续时间。用该化合物对去卵巢未成熟大鼠进行预处理会导致细胞质雌激素受体(ER)转位至细胞核,并使细胞质ER库显著减少,导致子宫在第4天之前对随后给予的雌激素无反应。而在用雌二醇预处理的大鼠中,细胞质ER水平升高使子宫对第二次注射的雌激素有反应。在延迟着床模型中,在抗雌激素治疗后第4、5或6天给经85/287预处理的大鼠注射雌酮。在第4天注射雌酮后未观察到着床,但在第5或6天给予雌酮时出现了着床。这些结果的总结表明,85/287在大鼠中的作用持续时间为3至4天。

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