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Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia

Preeclampsia is a complication of pregnancy characterised by gestational hypertension, proteinuria and/or end organ disease. The reduced uteroplacental perfusion (RUPP) model, via partial occlusion of the lower abdominal aorta, mimics insufficient placental perfusion as a primary causal characterist...

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Autores principales: Morton, J. S., Levasseur, J., Ganguly, E., Quon, A., Kirschenman, R., Dyck, J. R. B., Fraser, G. M., Davidge, S. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606748/
https://www.ncbi.nlm.nih.gov/pubmed/31266978
http://dx.doi.org/10.1038/s41598-019-45959-6
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author Morton, J. S.
Levasseur, J.
Ganguly, E.
Quon, A.
Kirschenman, R.
Dyck, J. R. B.
Fraser, G. M.
Davidge, S. T.
author_facet Morton, J. S.
Levasseur, J.
Ganguly, E.
Quon, A.
Kirschenman, R.
Dyck, J. R. B.
Fraser, G. M.
Davidge, S. T.
author_sort Morton, J. S.
collection PubMed
description Preeclampsia is a complication of pregnancy characterised by gestational hypertension, proteinuria and/or end organ disease. The reduced uteroplacental perfusion (RUPP) model, via partial occlusion of the lower abdominal aorta, mimics insufficient placental perfusion as a primary causal characteristic of preeclampsia. However, a major limitation of the RUPP model is that perfusion is reduced to the entire hindquarters of the rat resulting in hindlimb ischemia. We hypothesised that clipping the uterine and ovarian arteries in the selective (s)RUPP model would provoke signs of preeclampsia while avoiding systemic ischemia. Sham, RUPP or sRUPP procedures were performed in pregnant Sprague Dawley rats on gestational day (GD)14. On GD21 uterine blood flow was significantly reduced in both the RUPP and sRUPP models while aortic flow was reduced only in RUPP. Both models resulted in increased MAP, increased vascular oxidative stress (superoxide generation), increased pro-inflammatory (RANTES) and reduced pro-angiogenic (endoglin) mediators. Vascular compliance and constriction were unaltered in either RUPP or sRUPP groups. In summary, refinements to the RUPP model simultaneously maintain the characteristic phenotype of preeclampsia and avoid peripheral ischemia; providing a useful tool which may be used to increase our knowledge and bring us closer to a solution for women affected by preeclampsia.
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spelling pubmed-66067482019-07-14 Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia Morton, J. S. Levasseur, J. Ganguly, E. Quon, A. Kirschenman, R. Dyck, J. R. B. Fraser, G. M. Davidge, S. T. Sci Rep Article Preeclampsia is a complication of pregnancy characterised by gestational hypertension, proteinuria and/or end organ disease. The reduced uteroplacental perfusion (RUPP) model, via partial occlusion of the lower abdominal aorta, mimics insufficient placental perfusion as a primary causal characteristic of preeclampsia. However, a major limitation of the RUPP model is that perfusion is reduced to the entire hindquarters of the rat resulting in hindlimb ischemia. We hypothesised that clipping the uterine and ovarian arteries in the selective (s)RUPP model would provoke signs of preeclampsia while avoiding systemic ischemia. Sham, RUPP or sRUPP procedures were performed in pregnant Sprague Dawley rats on gestational day (GD)14. On GD21 uterine blood flow was significantly reduced in both the RUPP and sRUPP models while aortic flow was reduced only in RUPP. Both models resulted in increased MAP, increased vascular oxidative stress (superoxide generation), increased pro-inflammatory (RANTES) and reduced pro-angiogenic (endoglin) mediators. Vascular compliance and constriction were unaltered in either RUPP or sRUPP groups. In summary, refinements to the RUPP model simultaneously maintain the characteristic phenotype of preeclampsia and avoid peripheral ischemia; providing a useful tool which may be used to increase our knowledge and bring us closer to a solution for women affected by preeclampsia. Nature Publishing Group UK 2019-07-02 /pmc/articles/PMC6606748/ /pubmed/31266978 http://dx.doi.org/10.1038/s41598-019-45959-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Morton, J. S.
Levasseur, J.
Ganguly, E.
Quon, A.
Kirschenman, R.
Dyck, J. R. B.
Fraser, G. M.
Davidge, S. T.
Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title_full Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title_fullStr Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title_full_unstemmed Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title_short Characterisation of the Selective Reduced Uteroplacental Perfusion (sRUPP) Model of Preeclampsia
title_sort characterisation of the selective reduced uteroplacental perfusion (srupp) model of preeclampsia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6606748/
https://www.ncbi.nlm.nih.gov/pubmed/31266978
http://dx.doi.org/10.1038/s41598-019-45959-6
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