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输卵管、子宫及体外环境对小鼠胚胎透明带变薄的影响。

The effect of the oviduct, uterine, and in vitro environments on zona thinning in the mouse embryo.

作者信息

Confino E, Rawlins R, Binor Z, Radwanska E

机构信息

Division of Reproductive Endocrinology and Infertility, Rush Presbyterian St. Luke's Medical Center, Chicago, Illinois, USA.

出版信息

Fertil Steril. 1997 Jul;68(1):164-7. doi: 10.1016/s0015-0282(97)81495-1.

Abstract

OBJECTIVE

To evaluate the impact of the oviduct, uterine, and in vitro environments on zona pellucida thinning in the mouse embryo.

DESIGN

Female mice were stimulated with pregnant mare serum gonadotropin and mated and hCG injection. Unilateral oviduct ligation was performed on day 2 of gestation using the dorsal approach. The mice were divided into equal groups and killed on days 2, 3, 4, 5, and 10 of gestation. In vitro incubated embryos served as controls. Average daily zona thickness measurements were subjected to analysis of variance and paired Student's t-test.

SETTING

The laboratory of the assisted reproductive program of Rush University Medical Center.

MAIN OUTCOME MEASURE(S): Progressive daily decrease in average zona thickness.

RESULT(S): Zona measurements of embryos flushed out of uterine horns, ligated oviducts, and in vitro incubation demonstrated statistically significant decreases in zona thickness, from 9.6 +/- 1.6 microns (day 3) to 6.0 +/- 0.8 microns (day 5), from 11.6 +/- 2.2 microns (day 2) to 6.0 +/- 1.6 microns (day 5), and from 11.1 +/- 2.0 microns (day 2) to 6.0 +/- 1.6 microns (day 5), respectively. There were no differences in average zona thickness for embryos in the same cell stage and same protocol day in all three locations.

CONCLUSION(S): Zona thinning seems to be induced primarily by the dividing embryo before implantation. A substantial tubal and uterine contribution to zona thinning was not detected in this mouse embryo model.

摘要

目的

评估输卵管、子宫和体外环境对小鼠胚胎透明带变薄的影响。

设计

用孕马血清促性腺激素刺激雌性小鼠并进行交配及注射人绒毛膜促性腺激素。在妊娠第2天采用背部入路进行单侧输卵管结扎。将小鼠分成相等的组,并在妊娠第2、3、4、5和10天处死。体外培养的胚胎作为对照。对平均每日透明带厚度测量值进行方差分析和配对学生t检验。

地点

拉什大学医学中心辅助生殖项目实验室。

主要观察指标

透明带平均厚度的每日逐渐减少。

结果

从子宫角冲出、结扎输卵管及体外培养的胚胎的透明带测量显示,透明带厚度有统计学显著下降,分别从9.6±1.6微米(第3天)降至6.0±0.8微米(第5天),从11.6±2.2微米(第2天)降至6.0±1.6微米(第5天),以及从11.1±2.0微米(第2天)降至6.0±1.6微米(第5天)。在所有三个位置,处于相同细胞阶段和相同实验方案日的胚胎的透明带平均厚度没有差异。

结论

透明带变薄似乎主要由植入前分裂的胚胎诱导。在这个小鼠胚胎模型中未检测到输卵管和子宫对透明带变薄有显著作用。

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