期刊文献+

Postcoital Administration of Asoprisnil Inhibited Embryo Implantation and Disturbed Ultrastructure of Endometrium in Implantation Window in Mice

Postcoital Administration of Asoprisnil Inhibited Embryo Implantation and Disturbed Ultrastructure of Endometrium in Implantation Window in Mice
下载PDF
导出
摘要 Asoprisnil, a member of the selective progesterone receptor modulators, exerts high proges- terone receptor selectivity, endometrial targeted advantages and significant anti-implantation effect in rats. The purpose of this study was to confirm the anti-implantation effect of asoprisil, investigate the ultrastructural changes of the peri-implantation endometrium in mice and explore the effect of asoprisnil on endometrial receptivity and its targeted contraceptive proficiency. Post-coitus mice were adminis- tered with different dosages (0.2, 0.1, 0.05 mg·g^-1·day^-1) of asoprisnil from day 1 of pregnancy to day 3. Then 3 animals in each group were killed on day 5 of pregnancy, and uteri were collected to examine the ultrastructural changes of endometria under a transmission electron microscope (TEM). A total of 80 animals were sacrificed on day 8 of pregnancy, and the uterine horns were examined for the presence or absence of nidation sites and the number of implantation embryos. The results showed that the implan- tation rate and the average number of implantation embryos in asoprisnil groups were statistically sig- nificantly decreased as compared with the vehicle control group (P〈0.05). The TEM results revealed that, in vehicle control group, the tight junction between the luminal epithelia cells was short and straight, the gap was wide; the luminal epithelia cells were covered with plenty of short, clavate and neatly arranged microvilli; the endometril stromal cells were large with plenty of cytoplasm, and showed significant decidual change; there was more than one nucleus in stromal cells, and the karyotheca was integrity. In low dosage and high dosage asoprisnil groups, the tight junction was longer and more curve than in the vehicle control group; microvilli were uneven and asymmetrically distrib- uted in luminal epithelia; the stromal cells were small and the decidual change was not significant; there were karyopyknosis and karyolysis in stromal cells; there were abnormal thick-wall vessels in the en- dometrium. It was suggested that asoprisnil changed the ultrastructure of the endometrium in implantation window, disturbed the endometrial receptivity and finally resulted in embryo implantation failure. Asoprisnil, a member of the selective progesterone receptor modulators, exerts high proges- terone receptor selectivity, endometrial targeted advantages and significant anti-implantation effect in rats. The purpose of this study was to confirm the anti-implantation effect of asoprisil, investigate the ultrastructural changes of the peri-implantation endometrium in mice and explore the effect of asoprisnil on endometrial receptivity and its targeted contraceptive proficiency. Post-coitus mice were adminis- tered with different dosages (0.2, 0.1, 0.05 mg·g^-1·day^-1) of asoprisnil from day 1 of pregnancy to day 3. Then 3 animals in each group were killed on day 5 of pregnancy, and uteri were collected to examine the ultrastructural changes of endometria under a transmission electron microscope (TEM). A total of 80 animals were sacrificed on day 8 of pregnancy, and the uterine horns were examined for the presence or absence of nidation sites and the number of implantation embryos. The results showed that the implan- tation rate and the average number of implantation embryos in asoprisnil groups were statistically sig- nificantly decreased as compared with the vehicle control group (P〈0.05). The TEM results revealed that, in vehicle control group, the tight junction between the luminal epithelia cells was short and straight, the gap was wide; the luminal epithelia cells were covered with plenty of short, clavate and neatly arranged microvilli; the endometril stromal cells were large with plenty of cytoplasm, and showed significant decidual change; there was more than one nucleus in stromal cells, and the karyotheca was integrity. In low dosage and high dosage asoprisnil groups, the tight junction was longer and more curve than in the vehicle control group; microvilli were uneven and asymmetrically distrib- uted in luminal epithelia; the stromal cells were small and the decidual change was not significant; there were karyopyknosis and karyolysis in stromal cells; there were abnormal thick-wall vessels in the en- dometrium. It was suggested that asoprisnil changed the ultrastructure of the endometrium in implantation window, disturbed the endometrial receptivity and finally resulted in embryo implantation failure.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2013年第2期277-283,共7页 华中科技大学学报(医学英德文版)
基金 supported by Population and Family Planning Commission of Hubei Province,China(No.JS-2010004)
关键词 Asoprisnil ANTI-IMPLANTATION tight junction Asoprisnil anti-implantation tight junction
  • 相关文献

参考文献1

二级参考文献12

  • 1Lopata A. Implantation of the human embryo. Hum Reprod. 1996,11:175-184.
  • 2Psychoyos A, Mandon P. Study of the surface of the uterine epithelium by scanning electron microscope. Observations in the rat at the 4th and 5th day of pregnancy. C R Acad Sci Hebd Seances Acad Sci D,1971,272:2723-2725.
  • 3Enders AC, Nelson DM. Pinocytotic activity of the uterus of the rat.Am J Anat,1973, 138:277-299.
  • 4Nikas G, Makrigiannakis A, Hovatta O, et al. Surface morphology of the human endometrium. Basic and clinical aspects. Ann N Y Acad Sci, 2000,900:316-324.
  • 5Psychoyos A, Nikas G. Uterine pinopodes as markers of uterine receptivity. Ass Reprod Rev, 1994,4:26-32.
  • 6Nardo LG, Nikas G, Makrigiannakis A, et al. Synchronous expression of pinopodes and alpha v beta 3 and alpha 4 beta 1 integrins in the endometrial surface epithelium of normally menstruating women during the implantation window. J Reprod Med,2003,48:355-3
  • 7Stavreus-Evers A, Aghajanova L, Brismar H, et al. Co-existence of heparin-binding epidermal growth factor-like growth factor and pinopodes in human endometrium at the time of implantation. Mol Hum Reprod, 2002,8:765-769.
  • 8Aghajanova L, Stavreus-Evers A, Nikas Y, et al. Coexpression of pinopodes and leukemia inhibitory factor, as well as its receptor, in human endometrium. Fertil Steril, 2003,79:808-814.
  • 9Bentin-Ley U, Sjogren A, Nilsson L, et al. Presence of uterine pinopodes at the embryo-endometrial interface during human implantation in vitro. Hum Reprod,1999, 14:515-520.
  • 10Singh MM, Chauhan SC, Trivedi RN, et al. Correlation of pinopod development on uterine luminal epithelial surface with hormonal events and endometrial sensitivity in rat. Eur J Endocrinol,1996,135:107-117.

共引文献30

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部