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恒河猴黄体期早期单剂量给予米非司酮(RU486)对着床期子宫内膜的影响。

Effect of single-dose, early luteal phase administration of mifepristone (RU486) on implantation stage endometrium in the rhesus monkey.

作者信息

Ghosh D, Sengupta J, Hendrickx A G

机构信息

Department of Physiology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Hum Reprod. 1996 Sep;11(9):2026-35. doi: 10.1093/oxfordjournals.humrep.a019538.

Abstract

The characteristics of implantation stage endometrium following a single-dose, early luteal phase application of mifepristone (RU486) in proven conception cycles has been examined in the rhesus monkey in an attempt to understand the physiological basis of the anti-implantation activity of the drug. Endometrial samples were collected from monkeys subjected to vehicle (group 1, n = 14) and RU486 (2 mg/kg body weight; group 2, n = 12) on day 2 after the presumed day of ovulation of successfully mated cycles. The average diameter of glands (P < 0.05), number of vacuolated cells (P < 0.01), number of supranuclear vacuolated cells (P < 0.05) in glandular epithelium and amount of glandular secretion (P < 0.05) were significantly lower in RU486-treated endometrium compared with control tissue samples. Additionally, 18% of glandular epithelial cells showed apoptotic and degenerative features in RU486-treated tissue samples. These data, together with the observed significant decreases in precipitate area (P < 0.02) and in the optical absorbance of alkaline phosphatase reaction end-product (P < 0.05), confirm that retardation in glandular differentiation in the upper functionalis is a likely target of antiprogestin action in implantation stage endometrium. An increased frequency of mitosis in stromal cells (P < 0.05) and a greater degree of extravasation (P < 0.05) were also observed after RU486 exposure. Despite an apparent indication of constriction and regression in few RU486-exposed endometria compared with controls, morphometric analyses did not show any changes in capillary structure. Whether endometrial vasculature in progesterone-exposed uterus is a target of antiprogestin action during the peri-implantation stage remains to be determined. Further studies are required to explain the observed increase (P < 0.02) in the area of precipitate of von Willebrand (vW) factor with no change in vW factor-positive vessels, and the apparent increase in collagen IV immunostain in subepithelial and perivascular basement membrane in implantation stage endometrium after early luteal phase RU486 treatment in monkeys.

摘要

为了理解米非司酮(RU486)抗着床活性的生理基础,研究人员在恒河猴已证实的受孕周期中,于黄体期早期单剂量应用米非司酮后,对着床期子宫内膜的特征进行了研究。在假定成功交配周期排卵日之后的第2天,从接受赋形剂处理的猴子(第1组,n = 14)和接受RU486(2 mg/kg体重;第2组,n = 12)处理的猴子身上采集子宫内膜样本。与对照组织样本相比,RU486处理的子宫内膜中腺体的平均直径(P < 0.05)、空泡化细胞数量(P < 0.01)、腺上皮细胞核上空泡化细胞数量(P < 0.05)以及腺体分泌量(P < 0.05)均显著降低。此外,在RU486处理的组织样本中,18%的腺上皮细胞呈现出凋亡和退行性特征。这些数据,连同观察到的沉淀面积显著减少(P < 0.02)以及碱性磷酸酶反应终产物的光吸收显著降低(P < 0.05),证实了功能层上部腺体分化的延迟可能是抗孕激素在着床期子宫内膜中作用的靶点。在暴露于RU486后,还观察到基质细胞有丝分裂频率增加(P < 0.05)以及渗出程度增加(P < 0.05)。尽管与对照组相比,少数暴露于RU486的子宫内膜有收缩和退化的明显迹象,但形态计量分析未显示毛细血管结构有任何变化。在围植入期,孕激素暴露子宫中的子宫内膜血管系统是否是抗孕激素作用靶点仍有待确定。需要进一步研究来解释观察到的血管性血友病因子(vW)沉淀面积增加(P < 0.02)而vW因子阳性血管无变化,以及猴子在黄体期早期接受RU486处理后着床期子宫内膜上皮下和血管周围基底膜中IV型胶原免疫染色明显增加的现象。

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