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在正常妊娠和妊娠晚期的子宫胎盘单位中,AT1、AT2 和 AT(1-7) 受体的表达。

AT1, AT2, and AT(1-7) receptor expression in the uteroplacental unit of normotensive and hypertensive rats during early and late pregnancy.

机构信息

Hypertension and Vascular Research Center, Wake Forest School of Medicine, Winston-Salem, North Carolina 27157-1032, USA.

出版信息

Placenta. 2013 Jun;34(6):497-502. doi: 10.1016/j.placenta.2013.03.008. Epub 2013 Apr 17.

Abstract

INTRODUCTION

We investigated the expression of angiotensin receptors in early pregnancy and established whether normal pregnancy or preeclampsia alters the expression and distribution of the uteroplacental AT1R, AT2R and mas/AT1-7R at late gestation.

METHODS

The percentage of each receptor subtype present in tissues from virgin rats and from normotensive and RUPP hypertensive pregnant rats was established by in vitro receptor autoradiography. Receptor mRNA levels were determined by quantitative PCR at early and late pregnancy.

RESULTS

AT1R mRNA levels were up-regulated in the interimplantation (IIS) site at day 7 of gestation. AT2R mRNA levels were decreased at day 5 and 7 in the IIS but increased in the implantation site (IS) at day 5 and 7 as compared to the IIS at day 5. Mas/AT1-7R mRNA was increased in early pregnancy. In normal pregnancy and RUPP the mRNA for all angiotensin receptors was reduced in the uterus at late gestation. The AT1R accounted for the majority of binding in the uterus of virgin and the placenta of pregnant and RUPP. In RUPP pregnancy there was a significant competition with d-Ala in the placenta labyrinth.

DISCUSSION AND CONCLUSION

The expression of angiotensin receptors suggests their involvement in the maintenance of early stages of pregnancy. During late gestation down-regulation of Ang receptors in the uterus may arise from feedback down-regulation by Ang II. In the placenta the levels of AT1Rs are equivalent in the RUPP model. The increased binding of mas/AT1-7R at late gestation in RUPP may represent a compensatory mechanism to reduce uteroplacental vascular resistance.

摘要

简介

我们研究了血管紧张素受体在早孕中的表达,并确定正常妊娠或子痫前期是否会改变晚期妊娠时的子宫胎盘 AT1R、AT2R 和 mas/AT1-7R 的表达和分布。

方法

通过体外受体放射自显影术确定 virgin 大鼠组织和正常妊娠及 RUPP 高血压妊娠大鼠组织中各受体亚型的比例。通过定量 PCR 测定早期和晚期妊娠时的受体 mRNA 水平。

结果

AT1R mRNA 水平在妊娠第 7 天的种植前(IIS)部位上调。AT2R mRNA 水平在第 5 天和第 7 天的 IIS 中降低,但在第 5 天和第 7 天的植入部位(IS)中增加,与第 5 天的 IIS 相比。Mas/AT1-7R mRNA 在早孕时增加。在正常妊娠和 RUPP 中,所有血管紧张素受体的 mRNA 在晚期妊娠时在子宫中减少。AT1R 在 virgin 子宫和胎盘的妊娠和 RUPP 中占大部分结合。在 RUPP 妊娠中,胎盘迷路中与 d-Ala 有显著竞争。

讨论和结论

血管紧张素受体的表达表明其参与维持早期妊娠。在妊娠晚期,子宫中血管紧张素受体的下调可能是由 Ang II 的反馈下调引起的。在胎盘,RUPP 模型中 AT1Rs 的水平相当。RUPP 中晚期 mas/AT1-7R 结合的增加可能代表一种补偿机制,以降低胎盘血管阻力。

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