Singh M M, Chauhan S C, Trivedi R N, Maitra S C, Kamboj V P
Division of Endocrinology, Central Drug Research Institute, Lucknow, India.
Eur J Endocrinol. 1996 Jul;135(1):107-17. doi: 10.1530/eje.0.1350107.
Intrinsic role of preovulatory and nidatory estrogen and progesterone and presence of viable blastocysts in utero in pinopod development on the uterine luminal epithelial surface and correlation between time of their development and onset of endometrial sensitivity were investigated. In adult rats, pinopods were observed on the entire epithelium even before secretion of nidatory estrogen, i.e. at 14.00 h on day 4 post-coitum (p.c.). Apparently, their number increased, more so on the antimesometrial than the mesometrial side, at 10.00 h on day 5, but were fewer and mostly collapsed at 10.00 h on day 6. Pinopods on day 4 were located within epithelial depressions and foldings, but protruded from the surface on days 5 and 6. Normal pinopods were also present on day 8 p.c. in rats under delayed implantation, but an implantation-inducing dose of estradiol-17 beta administered about 18 h earlier caused their collapse like that on day 6 in intact rats. Development and appearance of pinopods in intact or delayed rats was unaffected when native preimplantation embryos were prevented from entering the uterus. Normal pinopods were seen in immature rats receiving progesterone for at least 3 days or cyproterone acetate for 4 days, but not after estradiol alone. In animals receiving progesterone or priming/sensitizing estradiol in addition to progesterone, the decidual response was suboptimal, irrespective of the presence of pinopods on the day of stimulation. In animals in which a condition mimicking preimplantation had been produced by suitable hormone supplementation, optimal endometrial sensitivity and decidual response were elicited, even though most pinopods appeared collapsed, resembling those on day 6 in intact rats and about 18 h after estradiol in implantation-delayed rats. Findings confirm that pinopod development on uterine luminal epithelium was dependent on progesterone alone and demonstrate that: (i) preovulatory (priming) or nidatory (endometrial sensitizing) estrogen or viable blastocysts in utero have no role in their development. Nidatory estrogen, instead, appears to limit pinopod development by causing their collapse; (ii) pinopod development/presence on the endometrial surface might indicate the uterus coming into a period of sensitivity rather than actually being in it and might thus serve as a useful marker of "transfer window" rather than "implantation window"; (iii) in the rat, pinopod development might serve as an alternate assay for evaluation of progestational activity of newer test agents.
研究了排卵前及着床期雌激素和孕酮的内在作用、子宫内活胚泡的存在对子宫腔上皮表面微绒毛形成的影响,以及它们的发育时间与子宫内膜敏感性开始之间的相关性。在成年大鼠中,甚至在着床期雌激素分泌之前,即在交配后第4天14:00时,整个上皮表面就观察到了微绒毛。显然,在第5天10:00时,微绒毛数量增加,子宫系膜对侧比子宫系膜侧增加得更多,但在第6天10:00时数量减少且大多塌陷。第4天的微绒毛位于上皮凹陷和褶皱内,但在第5天和第6天从表面突出。在延迟着床的大鼠中,妊娠第8天子宫腔上皮表面也有正常微绒毛,但提前约18小时给予诱导着床剂量的17β-雌二醇会导致其像正常大鼠第6天那样塌陷。当阻止着床前胚胎进入子宫时,正常或延迟大鼠中微绒毛的发育和外观不受影响。在接受至少3天孕酮或4天醋酸环丙孕酮的未成熟大鼠中可见正常微绒毛,但单独给予雌二醇后则未见。在接受孕酮或除孕酮外还给予引发/致敏雌二醇的动物中,无论刺激当天是否存在微绒毛,蜕膜反应都不理想。在通过适当激素补充产生类似着床前状态的动物中,即使大多数微绒毛看起来塌陷,类似于正常大鼠第6天以及延迟着床大鼠给予雌二醇后约18小时的微绒毛,也能引发最佳的子宫内膜敏感性和蜕膜反应。研究结果证实,子宫腔上皮表面微绒毛的发育仅依赖于孕酮,并表明:(i)排卵前(引发)或着床期(使子宫内膜致敏)雌激素或子宫内活胚泡对其发育无作用。相反,着床期雌激素似乎通过导致微绒毛塌陷来限制其发育;(ii)子宫内膜表面微绒毛的发育/存在可能表明子宫进入了一个敏感时期,而不是实际上处于该时期,因此可能作为“转移窗”而非“着床窗”的有用标志物;(iii)在大鼠中,微绒毛的发育可能作为评估新型测试药物孕激素活性的替代试验。