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子痫前期转基因大鼠模型的中肠系膜三角区血管紧张素 II 增加。

Increased angiotensin II in the mesometrial triangle of a transgenic rat model of preeclampsia.

机构信息

Wake Forest University Health Sciences, Winston-Salem, NC 27157-1032, USA.

出版信息

Hypertension. 2010 Feb;55(2):562-6. doi: 10.1161/HYPERTENSIONAHA.109.145656. Epub 2009 Dec 28.

Abstract

The pregnant female human angiotensinogen (hAGN) transgenic rat mated with the male hrenin (hREN) transgenic rat is a model of preeclampsia with increased blood pressure, proteinuria, and placenta alterations of edema and necrosis. The reverse mating of female hRENxmale hAGN does not show preeclamptic features. Because the placenta is well-recognized to be a key contributor to the preeclamptic syndrome, our hypothesis is that local angiotensin peptide concentrations found in the placenta and its associated mesometrial triangle of the preeclamptic transgenic rat differ from the reverse mating. We characterized the angiotensin peptide content and the mRNA expression of hREN and hAGN of the mesometrial triangle and the placenta. Three groups of pregnant rats from the matings (Sprague-DawleyxSprague-Dawley, reverse mating, and female hAGNxmale hREN) were studied on day 21 of gestation. In the hAGNxhREN transgenic rat, angiotensin II is significantly increased in the placenta and mesometrial triangle vs Sprague-Dawley (24.2+/-3.9 vs 8.6+/-1.5 pg/mg protein; 27.8+/-5.5 vs 5.6+/-1.3 pg/mg protein; P<0.05), whereas in the reverse mating angiotensin II is increased in the placenta (19.1+/-1.7 vs 5.6+/-1.3 pg/mg protein; P<0.05) but unchanged in the mesometrial triangle (4.2+/-0.2 vs 8.6+/-1.5 pg/mg protein). The marked contrast in the expression of angiotensin II in the mesometrial triangle of the preeclamptic model vs the reverse mating suggests that local angiotensin II generated from the maternal parts of the uteroplacental unit may play a critical role in preeclampsia.

摘要

人血管紧张素原(hAGN)转基因雌性大鼠与血管紧张素原(hREN)转基因雄性大鼠交配,可形成高血压、蛋白尿、胎盘水肿和坏死改变的子痫前期模型。反向交配的雌性 hRENx 雄性 hAGN 则不表现出子痫前期特征。由于胎盘被公认为子痫前期综合征的关键贡献者,我们的假设是,在子痫前期转基因大鼠的胎盘及其相关的中肾旁三角中发现的局部血管紧张素肽浓度与反向交配不同。我们对中肾旁三角和胎盘的血管紧张素肽含量以及 hREN 和 hAGN 的 mRNA 表达进行了特征描述。对来自交配的三组怀孕大鼠(Sprague-DawleyxSprague-Dawley、反向交配和雌性 hAGNx 雄性 hREN)进行了研究,研究时间为妊娠第 21 天。在 hAGNxhREN 转基因大鼠中,胎盘和中肾旁三角的血管紧张素 II 显著高于 Sprague-Dawley(24.2+/-3.9 对 8.6+/-1.5 pg/mg 蛋白;27.8+/-5.5 对 5.6+/-1.3 pg/mg 蛋白;P<0.05),而在反向交配中,胎盘中的血管紧张素 II 增加(19.1+/-1.7 对 5.6+/-1.3 pg/mg 蛋白;P<0.05),但中肾旁三角不变(4.2+/-0.2 对 8.6+/-1.5 pg/mg 蛋白)。在子痫前期模型的中肾旁三角中血管紧张素 II 的表达与反向交配的显著对比表明,来自母体子宫胎盘单位的局部血管紧张素 II 可能在子痫前期中发挥关键作用。

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