From the Department of Pharmacology (A.R.N., S.D.S., L.N.A., J.W., P.N., M.M., K.-T.L., J.A.S., J.L.G., C.D.S.), Roy J. and Lucille A. Carver College of Medicine, University of Iowa.
Department of Physiology, Cardiovascular Center, Medical College of Wisconsin, Milwaukee (S.D.S., J.W., P.N., K.-T.L., J.L.G., C.D.S.).
Hypertension. 2019 Jul;74(1):173-183. doi: 10.1161/HYPERTENSIONAHA.119.13101. Epub 2019 May 20.
Preeclampsia is a hypertensive disorder of pregnancy associated with vascular dysfunction and cardiovascular risk to offspring. We hypothesize that endothelial PPARγ (peroxisome proliferator-activated receptor-γ) provides cardiovascular protection in offspring from pregnancies complicated by hypertension. C57BL/6J dams were bred with E-V290M sires, which express a dominant-negative allele of PPARγ selectively in the endothelium. Arginine vasopressin was infused throughout gestation. Vasopressin elevated maternal blood pressure at gestational day 14 to 15 and urinary protein at day 17 consistent. Systolic blood pressure and vasodilation responses to acetylcholine were similar in vasopressin-exposed offspring compared to offspring from control pregnancies. We treated offspring with a subpressor dose of angiotensin II to test if hypertension during pregnancy predisposes offspring to hypertension. Male and female angiotensin II-treated E-V290M offspring from vasopressin-exposed but not control pregnancy exhibited significant impairment in acetylcholine-induced relaxation in carotid artery. Endothelial dysfunction in angiotensin II-treated E-V290M vasopressin-exposed offspring was attenuated by tempol, an effect which was more prominent in male offspring. Nrf2 (nuclear factor-E2-related factor) protein levels were significantly elevated in aorta from male E-V290M offspring, but not female offspring compared to controls. Blockade of ROCK (Rho-kinase) signaling and incubation with a ROCK2-specific inhibitor improved endothelial function in both male and female E-V290M offspring from vasopressin-exposed pregnancy. Our data suggest that interference with endothelial PPARγ in offspring from vasopressin-exposed pregnancies increases the risk for endothelial dysfunction on exposure to a cardiovascular stressor in adulthood. This implies that endothelial PPARγ provides protection to cardiovascular stressors in offspring of a pregnancy complicated by hypertension and perhaps in preeclampsia.
子痫前期是一种与血管功能障碍和心血管风险相关的妊娠高血压疾病。我们假设内皮细胞 PPARγ(过氧化物酶体增殖物激活受体-γ)为妊娠合并高血压的后代提供心血管保护。C57BL/6J 母鼠与表达内皮细胞选择性显性负效 PPARγ 的 E-V290M 父鼠交配,血管升压素在整个妊娠期输注。血管升压素在妊娠第 14-15 天使母体血压升高,并在第 17 天使尿蛋白升高。血管升压素暴露的后代与来自对照妊娠的后代相比,乙酰胆碱引起的收缩压和血管舒张反应相似。我们用亚加压素剂量的血管紧张素 II 治疗后代,以测试妊娠期间的高血压是否使后代易患高血压。来自血管升压素暴露但不是对照妊娠的雄性和雌性血管紧张素 II 处理的 E-V290M 后代的颈总动脉对乙酰胆碱诱导的舒张有明显的损害。血管紧张素 II 处理的 E-V290M 血管升压素暴露的后代中,内皮功能障碍被 tempol 减轻,这种作用在雄性后代中更为明显。与对照组相比,雄性 E-V290M 后代的主动脉中 Nrf2(核因子-E2 相关因子)蛋白水平显著升高,但雌性后代没有。阻断 ROCK(Rho 激酶)信号和用 ROCK2 特异性抑制剂孵育可改善血管升压素暴露妊娠的雄性和雌性 E-V290M 后代的内皮功能。我们的数据表明,在血管升压素暴露的后代中干扰内皮细胞 PPARγ,会增加成年后暴露于心血管应激源时发生内皮功能障碍的风险。这意味着内皮细胞 PPARγ为妊娠合并高血压的后代提供了对心血管应激源的保护,也许在子痫前期中也是如此。