Peplow P V
Department of Anatomy, University of Otago, Dunedin, New Zealand.
Prostaglandins Leukot Essent Fatty Acids. 1991 Dec;44(4):217-22. doi: 10.1016/0952-3278(91)90020-6.
Ovariectomized early pregnant rats given continuous steroid replacement therapy have been treated with antiprogesterone steroid, ZK98299 or RU38486. At 24 h following treatment, uterine explants in culture were found to produce significantly greater amounts of PGF2 alpha, but not of 6-keto-PGF1 alpha, when compared to controls. ZK98299 and RU38486 gave almost identical levels of uterine PG production. The 6-keto-PGF1 alpha/PGF2 alpha production ratio for uteri of treated rats was decreased by 45% relative to controls. Similar changes in uterine PGF2 alpha production and 6-keto-PGF1 alpha/PGF2 alpha ratio have been shown for ovariectomized early pregnant rats in which progesterone has been withdrawn when compared to control animals. It has been suggested that inhibiting or withdrawing progesterone in rat uteri exposed to estradiol and progesterone may lead to a stimulation of endoperoxide F-reductase and/or E2 9-ketoreductase activities. The presence of luminal fluid in the uteri was observed for animals treated with antiprogesterone steroid or in which progesterone had been withdrawn. This was associated with a decrease in % dry weight for the uteri of these animals.
对切除卵巢的早孕大鼠给予持续的类固醇替代疗法,并使用抗孕酮类固醇ZK98299或RU38486进行治疗。治疗后24小时发现,与对照组相比,培养的子宫外植体产生的前列腺素F2α(PGF2α)量显著增加,但6-酮-前列腺素F1α(6-keto-PGF1α)的量未增加。ZK98299和RU38486使子宫前列腺素的产生水平几乎相同。与对照组相比,接受治疗大鼠子宫的6-酮-前列腺素F1α/前列腺素F2α产生比率降低了45%。与对照动物相比,已显示切除卵巢的早孕大鼠在撤除孕酮后,子宫前列腺素F2α产生及6-酮-前列腺素F1α/前列腺素F2α比率有类似变化。有人提出,在暴露于雌二醇和孕酮的大鼠子宫中抑制或撤除孕酮可能会刺激内过氧化物F-还原酶和/或E2 9-酮还原酶的活性。在用抗孕酮类固醇治疗或已撤除孕酮的动物子宫中观察到有管腔液存在。这与这些动物子宫干重百分比的降低有关。