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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)
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    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)
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    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

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