Publication: Mechanisms of vascular dysfunction in the interleukin-10–deficient murine model of preeclampsia indicate nitric oxide dysregulation
| dc.contributor.author | Cubro, Hajrunisa (57194398691) | |
| dc.contributor.author | Nath, Karl A. (7102188130) | |
| dc.contributor.author | Suvakov, Sonja (36572404500) | |
| dc.contributor.author | Garcia-Valencia, Oscar (57205373508) | |
| dc.contributor.author | Parashuram, Santosh (57204718692) | |
| dc.contributor.author | White, Wendy M. (54279565800) | |
| dc.contributor.author | Weissgerber, Tracey L. (6506688349) | |
| dc.contributor.author | Nath, Meryl C. (57200731038) | |
| dc.contributor.author | Milic, Natasa M. (7003460927) | |
| dc.contributor.author | Sontag, Fernando (56245905600) | |
| dc.contributor.author | d'Uscio, Livius V. (6701488280) | |
| dc.contributor.author | Zhu, Yi (56589215600) | |
| dc.contributor.author | Kirkland, James L. (35594558800) | |
| dc.contributor.author | Tchkonia, Tamar (6508197068) | |
| dc.contributor.author | Alexander, Mariam P. (55201846000) | |
| dc.contributor.author | Quinton, Reade A. (7004911745) | |
| dc.contributor.author | Katusic, Zvonimir S. (7006971465) | |
| dc.contributor.author | Grande, Joseph P. (7004996226) | |
| dc.contributor.author | Garovic, Vesna D. (6603419874) | |
| dc.date.accessioned | 2025-06-12T13:40:47Z | |
| dc.date.available | 2025-06-12T13:40:47Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | 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 | |
| dc.identifier.uri | https://doi.org/10.1016/j.kint.2020.09.034 | |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85101331982&doi=10.1016%2fj.kint.2020.09.034&partnerID=40&md5=43909ed304fe7408d8fddf5b3b3bf2a5 | |
| dc.identifier.uri | https://remedy.med.bg.ac.rs/handle/123456789/4333 | |
| dc.subject | interleukin-10 | |
| dc.subject | mouse | |
| dc.subject | preeclampsia | |
| dc.subject | vascular reactivity | |
| dc.title | Mechanisms of vascular dysfunction in the interleukin-10–deficient murine model of preeclampsia indicate nitric oxide dysregulation | |
| dspace.entity.type | Publication |
