Browsing by Author "Sontag, Fernando (56245905600)"
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Publication Mechanisms of vascular dysfunction in the interleukin-10–deficient murine model of preeclampsia indicate nitric oxide dysregulation(2021) ;Cubro, Hajrunisa (57194398691) ;Nath, Karl A. (7102188130) ;Suvakov, Sonja (36572404500) ;Garcia-Valencia, Oscar (57205373508) ;Parashuram, Santosh (57204718692) ;White, Wendy M. (54279565800) ;Weissgerber, Tracey L. (6506688349) ;Nath, Meryl C. (57200731038) ;Milic, Natasa M. (7003460927) ;Sontag, Fernando (56245905600) ;d'Uscio, Livius V. (6701488280) ;Zhu, Yi (56589215600) ;Kirkland, James L. (35594558800) ;Tchkonia, Tamar (6508197068) ;Alexander, Mariam P. (55201846000) ;Quinton, Reade A. (7004911745) ;Katusic, Zvonimir S. (7006971465) ;Grande, Joseph P. (7004996226)Garovic, Vesna D. (6603419874)Preeclampsia is a pregnancy-specific hypertensive disorder characterized by proteinuria, and vascular injury in the second half of pregnancy. We hypothesized that endothelium-dependent vascular dysfunction is present in a murine model of preeclampsia based on administration of human preeclamptic sera to interleukin-10-/- mice and studied mechanisms that underlie vascular injury. Pregnant wild type and IL-10-/- mice were injected with either normotensive or severe preeclamptic patient sera (sPE) during gestation. A preeclampsia-like phenotype was confirmed by blood pressure measurements; assessment of albuminuria; measurement of angiogenic factors; demonstration of foot process effacement and endotheliosis in kidney sections; and by accumulation of glycogen in placentas from IL-10-/- mice injected with sPE sera (IL-10-/-sPE). Vasomotor function of isolated aortas was assessed. The IL-10-/-sPE murine model demonstrated significantly augmented aortic contractions to phenylephrine and both impaired endothelium-dependent and, to a lesser extent, endothelium-independent relaxation compared to wild type normotensive mice. Treatment of isolated aortas with indomethacin, a cyclooxygenase inhibitor, improved, but failed to normalize contraction to phenylephrine to that of wild type normotensive mice, suggesting the additional contribution from nitric oxide downregulation and effects of indomethacin-resistant vasoconstricting factors. In contrast, indomethacin normalized relaxation of aortas derived from IL-10-/-sPE mice. Thus, our results identify the role of IL-10 deficiency in dysregulation of the cyclooxygenase pathway and vascular dysfunction in the IL-10-/-sPE murine model of preeclampsia and point towards a possible contribution of nitric oxide dysregulation. These compounds and related mechanisms may serve both as diagnostic markers and therapeutic targets for preventive and treatment strategies in preeclampsia. © 2020 International Society of Nephrology
