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Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis

Fluid resuscitation following severe inflammation-induced hypoperfusion is critical for the restoration of hemodynamics and the prevention of multiorgan dysfunction syndrome during septic shock. Fluid resuscitation with commercially available crystalloid and colloid solutions only provides transient...

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Autores principales: Belcher, Donald A., Williams, Alexander T., Palmer, Andre F., Cabrales, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149844/
https://www.ncbi.nlm.nih.gov/pubmed/34035380
http://dx.doi.org/10.1038/s41598-021-90431-z
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author Belcher, Donald A.
Williams, Alexander T.
Palmer, Andre F.
Cabrales, Pedro
author_facet Belcher, Donald A.
Williams, Alexander T.
Palmer, Andre F.
Cabrales, Pedro
author_sort Belcher, Donald A.
collection PubMed
description Fluid resuscitation following severe inflammation-induced hypoperfusion is critical for the restoration of hemodynamics and the prevention of multiorgan dysfunction syndrome during septic shock. Fluid resuscitation with commercially available crystalloid and colloid solutions only provides transient benefits, followed by fluid extravasation and tissue edema through the inflamed endothelium. The increased molecular weight (M.W.) of polymerized human serum albumin (PolyHSA) can limit fluid extravasation, leading to restoration of hemodynamics. In this prospective study, we evaluated how fluid resuscitation with PolyHSA impacts the hemodynamic and immune response in a lipopolysaccharide (LPS) induced endotoxemia mouse model. Additionally, we evaluated fluid resuscitation with PolyHSA in a model of polymicrobial sepsis induced by cecal ligation and puncture (CLP). Resuscitation with PolyHSA attenuated the immune response and improved the maintenance of systemic hemodynamics and restoration of microcirculatory hemodynamics. This decrease in inflammatory immune response and maintenance of vascular wall shear stress likely contributes to the maintenance of vascular integrity following fluid resuscitation with PolyHSA. The sustained restoration of perfusion, decrease in pro-inflammatory immune response, and improved vascular integrity that results from the high M.W. of PolyHSA indicates that a PolyHSA based solution is a potential resuscitation fluid for endotoxic and septic shock.
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spelling pubmed-81498442021-05-26 Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis Belcher, Donald A. Williams, Alexander T. Palmer, Andre F. Cabrales, Pedro Sci Rep Article Fluid resuscitation following severe inflammation-induced hypoperfusion is critical for the restoration of hemodynamics and the prevention of multiorgan dysfunction syndrome during septic shock. Fluid resuscitation with commercially available crystalloid and colloid solutions only provides transient benefits, followed by fluid extravasation and tissue edema through the inflamed endothelium. The increased molecular weight (M.W.) of polymerized human serum albumin (PolyHSA) can limit fluid extravasation, leading to restoration of hemodynamics. In this prospective study, we evaluated how fluid resuscitation with PolyHSA impacts the hemodynamic and immune response in a lipopolysaccharide (LPS) induced endotoxemia mouse model. Additionally, we evaluated fluid resuscitation with PolyHSA in a model of polymicrobial sepsis induced by cecal ligation and puncture (CLP). Resuscitation with PolyHSA attenuated the immune response and improved the maintenance of systemic hemodynamics and restoration of microcirculatory hemodynamics. This decrease in inflammatory immune response and maintenance of vascular wall shear stress likely contributes to the maintenance of vascular integrity following fluid resuscitation with PolyHSA. The sustained restoration of perfusion, decrease in pro-inflammatory immune response, and improved vascular integrity that results from the high M.W. of PolyHSA indicates that a PolyHSA based solution is a potential resuscitation fluid for endotoxic and septic shock. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149844/ /pubmed/34035380 http://dx.doi.org/10.1038/s41598-021-90431-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Belcher, Donald A.
Williams, Alexander T.
Palmer, Andre F.
Cabrales, Pedro
Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title_full Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title_fullStr Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title_full_unstemmed Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title_short Polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
title_sort polymerized albumin restores impaired hemodynamics in endotoxemia and polymicrobial sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149844/
https://www.ncbi.nlm.nih.gov/pubmed/34035380
http://dx.doi.org/10.1038/s41598-021-90431-z
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