Paria B C, Das S K, Gupta A, Dey S K
Department of Obstetrics & Gynecology, University of Kansas Medical Center, Ralph L. Smith Research Center, Kansas City 66103.
Prostaglandins. 1991 Sep;42(3):191-9. doi: 10.1016/0090-6980(91)90109-s.
In the mouse, estriol (E3) can induce implantation as a phase I of estrogen action. E3-induced implantation was attenuated by indomethacin(INDO), an inhibitor of prostaglandin (PG) synthesis. The inhibitory effect of INDO was reversed by administration of epidermal growth factor (EGF), and this EGF effect was dose-dependent. These results suggest that one of the functions of estrogen could be to activate the EGF ligand-receptor signalling in the uterus in generating PGs required for initiation of implantation. This is consistent with the results of EGF stimulation of synthesis of PGs in uterine stromal cells in culture.
在小鼠中,雌三醇(E3)作为雌激素作用的第一阶段可诱导着床。吲哚美辛(INDO)是一种前列腺素(PG)合成抑制剂,它可减弱E3诱导的着床。表皮生长因子(EGF)给药可逆转INDO的抑制作用,且这种EGF效应呈剂量依赖性。这些结果表明,雌激素的功能之一可能是激活子宫中的EGF配体-受体信号,以产生着床起始所需的PG。这与培养的子宫基质细胞中EGF刺激PG合成的结果一致。