米非司酮和抗雌激素对去卵巢和妊娠大鼠子宫PGF2α和PGE2浓度的影响

Xue-Jun Li , He-ming Yu , Samuel S. Koide
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引用次数: 3

摘要

采用四种抗雌激素药物(anordiol, tamoxifen, ru39411, ICI 182780)和抗黄体酮米非司酮(mifepristone, ru486)分别给予3种动物模型:(1)去卵巢大鼠;(2)交配后处理的大鼠;(3)植入后处理的妊娠大鼠。抗雌激素单独或与米非司酮联合使用,剂量有效地预防和/或终止大鼠妊娠。本研究的目的是确定这些药物是否影响前列腺素(PGF2α和PGE2)的子宫浓度。去卵巢大鼠单独使用抗雌激素不影响子宫PGE2或PGF2α浓度;而氨二醇/米非司酮联合用药可使子宫内PGF2α浓度升高,导致PGF2α/PGE2比值升高。交配大鼠在性交后连续3天给予安诺二醇、他莫西芬、雌二醇和米非司酮单独或安诺二醇/米非司酮和他莫西芬/米非司酮联合治疗。子宫PGF2α浓度升高,PGF2α/PGE2比值升高,仅在异丙二醇/米非司酮治疗组发生。经异丙二醇、他莫昔芬和雌二醇处理的小鼠子宫PGE2浓度降低,导致PGF2α/PGE2比值升高。妊娠第7、8、9天分别给药Anordiol (5.0 mg/kg/day)和米非司酮(4.0 mg/kg/day)以及Anordiol /米非司酮(2.5/1.0 mg/kg/day)可诱导PGF2α水平升高,但不影响子宫PGE2浓度。anordiol及anordiol/米非司酮联合用药引起子宫PGF2α浓度变化,导致PGF2α/PGE2比值升高。除ICI 182780外,其余抗雌激素均具有增强去卵巢大鼠子宫重量的激动剂活性。此外,ICI 182789是唯一不影响子宫PG浓度的抗雌激素。可以得出结论,ICI 182780是所有测试中唯一的“纯”抗雌激素。本研究结果表明,抗雌激素和米非司酮联合异丙二醇在阻止着床和终止妊娠的剂量下增加子宫PGF2α和/或降低PGE2浓度,导致PGF2α/PGE2比值的改变。这些发现表明,子宫内PGF2α与PGE2浓度的平衡是受精卵正常通过输卵管、启动囊胚着床、胚胎发育和维持妊娠所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of mifepristone and antiestrogens on uterine PGF2α and PGE2 concentrations in ovariectomized and pregnant rats

Four antiestrogens (anordiol, tamoxifen, RU 39411, ICI 182780) and the antiprogestin, mifepristone (RU 486), were administered to the following three animal models: (1) ovariectomized rats, (2) mated rats treated post-coitally; and (3) pregnant rats treated post-implantation. The antiestrogens were administered alone or in combination with mifepristone at doses effective in preventing and/or terminating pregnancy in rats. The objective of the study was to determine whether these drugs influenced uterine concentrations of prostaglandins (PGF and PGE2).

Antiestrogens administered alone to ovariectomized rats did not effect uterine PGE2 or PGF concentrations; whereas the combination of anordiol/mifepristone increased uterine PGF concentration, resulting in an increase in the PGF/PGE2 ratio.

Mated rats were treated post-coitally for three consecutive days with anordiol, tamoxifen, estradiol and mifepristone alone and with the combination of anordiol/mifepristone and tamoxifen/mifepristone. An increase in uterine PGF concentrations and in the PGF/PGE2 ratio occurred only in anordiol/mifepristone treated group. A decrease in uterine PGE2 concentrations occurred in animals treated with anordiol, tamoxifen and estradiol, resulting in an increase in the PGF/PGE2 ratio.

Anordiol (5.0 mg/kg/day) and mifepristone (4.0 mg/kg/day) alone and the combination of anordiol/mifepristone (2.5/1.0 mg/kg/day) administered to pregnant rats on days 7, 8 and 9 of pregnancy induced an increase in PGF levels without affecting uterine PGE2 concentration. The changes in uterine PGF concentrations induced by anordiol and the combination of anordiol/mifepristone resulted in an increase in the PGF/PGE2 ratio.

The antiestrogens tested except for ICI 182780 possessed agonist activity when assayed by measuring their capacity to increase the uterine weights in ovariectomized rats. Also, ICI 182789 was the only antiestrogen that did not influence uterine PG concentrations. It can be concluded that ICI 182780 is the only “pure” antiestrogen among those tested.

The present results show that antiestrogens and the combination of mifepristone plus anordiol at doses preventing implantation and terminating pregnancy increase uterine PGF and/or decrease PGE2 concentrations, resulting in an alteration of PGF/PGE2 ratio. These findings suggest that there exists a critical balance of PGF to PGE2 concentrations in the uterus required for the normal passage of fertilized ova through the oviduct, initiating implantation of the blastocysts, development of embryos, and maintenance of pregnancy.

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