Placental hypoxia-induced alterations in vascular function, morphology, and endothelial barrier integrity

被引:0
作者
Philippe Vangrieken
Alex H. V. Remels
Salwan Al-Nasiry
Aalt Bast
Ger. M. J. Janssen
Ulrike von Rango
Daan Vroomans
Yannick C. W. Pinckers
Frederik J. van Schooten
Paul M. H. Schiffers
机构
[1] Maastricht University Medical Center+,School of Nutrition and Translational Research in Metabolism (NUTRIM), Department of Pharmacology and Toxicology
[2] Maastricht University Medical Center+,School for Oncology and Developmental Biology (GROW), Department of Obstetrics and Gynaecology
[3] Maastricht University Medical Center+,School for Cardiovascular Diseases (CARIM), Department of Pharmacology and Toxicology
[4] Maastricht University Medical Center+,Department of Anatomy and Embryology
来源
Hypertension Research | 2020年 / 43卷
关键词
Placental hypoxia; Preeclampsia; Hypertension; Endothelium; Vascular smooth muscle;
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中图分类号
学科分类号
摘要
Preeclampsia (PE) is a pregnancy-related disorder characterized by hypertension and proteinuria that affects 3–10% of all pregnancies. Although its pathophysiology remains obscure, placental hypoxia-induced oxidative stress and alterations in vascular function, morphology, and endothelial barrier integrity are considered to play a key role in the development of preeclampsia. In this study, placental villous explants of noncomplicated placentae and BeWo cells were subjected to hypoxia. The effect of placental hypoxic-conditioned medium (HCM) on intraluminal-induced contraction and endothelial barrier integrity in chorionic arteries was investigated using pressure myography. The impact of BeWo cell HCM on endothelial cell viability, reactive oxygen species formation and inflammation was also determined. Alterations in arterial morphology and contractile responsiveness to the thromboxane A2 analog (U46619) after exposure to placental HCM were examined immunohistochemically and by wire myography, respectively. Intraluminal administration of placental HCM induced vasoconstriction and increased the endothelial permeability for KCl, which was concentration-dependently prevented by quercetin. Placental and BeWo cell HCMs decreased endothelial cell viability, increased the production of reactive oxygen species and enhanced the secretion of IL-6 and IL-8. The cross-sectional area of the arterial media was increased upon exposure to placental HCM, which was associated with increased vascular proliferation and contractile responsiveness to U46619, and all of these effects were prevented by the antioxidants quercetin and RRR-α-tocopherol. This study is the first to comprehensively demonstrate the link between factors secreted by placental cells in response to hypoxia and vascular abnormalities and paves the way for new diagnostic approaches and therapies to better protect the maternal vasculature during and after a preeclampsia-complicated pregnancy.
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页码:1361 / 1374
页数:13
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