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Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis

BACKGROUND: Fluid resuscitation is a crucial therapy for sepsis, and the use of balanced fluids and/or isotonic albumin may improve patient survival. We have previously demonstrated that resuscitation with normal saline results in increased hepatic leukocyte recruitment in a murine model of sepsis....

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Autores principales: Patrick, Amanda L., Grin, Peter M., Kraus, Nicole, Gold, Michelle, Berardocco, Matthew, Liaw, Patricia C., Fox-Robichaud, Alison E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247397/
https://www.ncbi.nlm.nih.gov/pubmed/28105603
http://dx.doi.org/10.1186/s40635-017-0118-5
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author Patrick, Amanda L.
Grin, Peter M.
Kraus, Nicole
Gold, Michelle
Berardocco, Matthew
Liaw, Patricia C.
Fox-Robichaud, Alison E.
author_facet Patrick, Amanda L.
Grin, Peter M.
Kraus, Nicole
Gold, Michelle
Berardocco, Matthew
Liaw, Patricia C.
Fox-Robichaud, Alison E.
author_sort Patrick, Amanda L.
collection PubMed
description BACKGROUND: Fluid resuscitation is a crucial therapy for sepsis, and the use of balanced fluids and/or isotonic albumin may improve patient survival. We have previously demonstrated that resuscitation with normal saline results in increased hepatic leukocyte recruitment in a murine model of sepsis. Given that clinical formulations of albumin are in saline, our objectives were to develop a novel balanced electrolyte solution specifically for sepsis and to determine if supplementing this solution with albumin would improve the inflammatory response in sepsis. METHODS: We developed two novel buffered electrolyte solutions that contain different concentrations of acetate and gluconate, named Seplyte L and Seplyte H, and administered these solutions with or without 5% albumin. Normal saline with or without albumin and Ringer’s lactate served as controls. Sepsis was induced by cecal ligation and puncture (CLP), and the liver microvasculature was imaged in vivo at 6 h after CLP to quantify leukocyte recruitment. Hepatic cytokine expression and plasma cell-free DNA (cfDNA) concentrations were also measured. RESULTS: Septic mice receiving either Seplyte fluid showed significant reductions in hepatic post-sinusoidal leukocyte rolling and adhesion compared to normal saline. Hepatic cytokine concentrations varied in response to different concentrations of acetate and gluconate in the novel resuscitation fluids but were unaffected by albumin. All Seplyte fluids significantly increased hepatic TNF-α levels at 6 h compared to control fluids. However, Seplyte H exhibited a similar cytokine profile to the control fluids for all other cytokines, whereas mice given Seplyte L had significantly elevated IL-6, IL-10, KC (CXCL1), and MCP-1 (CCL2). Plasma cfDNA was generally increased during sepsis, but resuscitation fluid composition did not significantly affect cfDNA concentrations. CONCLUSIONS: Electrolyte concentrations and buffer constituents of resuscitation fluids can modulate hepatic cytokine production and leukocyte recruitment in septic mice, while the effects of albumin are modest during early sepsis. Therefore, crystalloid fluid choice should be an important consideration for resuscitation in sepsis, and the effects of fluid composition on inflammation in other organ systems should be studied to better understand the physiological impact of this vital sepsis therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40635-017-0118-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-52473972017-02-02 Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis Patrick, Amanda L. Grin, Peter M. Kraus, Nicole Gold, Michelle Berardocco, Matthew Liaw, Patricia C. Fox-Robichaud, Alison E. Intensive Care Med Exp Research BACKGROUND: Fluid resuscitation is a crucial therapy for sepsis, and the use of balanced fluids and/or isotonic albumin may improve patient survival. We have previously demonstrated that resuscitation with normal saline results in increased hepatic leukocyte recruitment in a murine model of sepsis. Given that clinical formulations of albumin are in saline, our objectives were to develop a novel balanced electrolyte solution specifically for sepsis and to determine if supplementing this solution with albumin would improve the inflammatory response in sepsis. METHODS: We developed two novel buffered electrolyte solutions that contain different concentrations of acetate and gluconate, named Seplyte L and Seplyte H, and administered these solutions with or without 5% albumin. Normal saline with or without albumin and Ringer’s lactate served as controls. Sepsis was induced by cecal ligation and puncture (CLP), and the liver microvasculature was imaged in vivo at 6 h after CLP to quantify leukocyte recruitment. Hepatic cytokine expression and plasma cell-free DNA (cfDNA) concentrations were also measured. RESULTS: Septic mice receiving either Seplyte fluid showed significant reductions in hepatic post-sinusoidal leukocyte rolling and adhesion compared to normal saline. Hepatic cytokine concentrations varied in response to different concentrations of acetate and gluconate in the novel resuscitation fluids but were unaffected by albumin. All Seplyte fluids significantly increased hepatic TNF-α levels at 6 h compared to control fluids. However, Seplyte H exhibited a similar cytokine profile to the control fluids for all other cytokines, whereas mice given Seplyte L had significantly elevated IL-6, IL-10, KC (CXCL1), and MCP-1 (CCL2). Plasma cfDNA was generally increased during sepsis, but resuscitation fluid composition did not significantly affect cfDNA concentrations. CONCLUSIONS: Electrolyte concentrations and buffer constituents of resuscitation fluids can modulate hepatic cytokine production and leukocyte recruitment in septic mice, while the effects of albumin are modest during early sepsis. Therefore, crystalloid fluid choice should be an important consideration for resuscitation in sepsis, and the effects of fluid composition on inflammation in other organ systems should be studied to better understand the physiological impact of this vital sepsis therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40635-017-0118-5) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-01-19 /pmc/articles/PMC5247397/ /pubmed/28105603 http://dx.doi.org/10.1186/s40635-017-0118-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research
Patrick, Amanda L.
Grin, Peter M.
Kraus, Nicole
Gold, Michelle
Berardocco, Matthew
Liaw, Patricia C.
Fox-Robichaud, Alison E.
Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title_full Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title_fullStr Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title_full_unstemmed Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title_short Resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
title_sort resuscitation fluid composition affects hepatic inflammation in a murine model of early sepsis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247397/
https://www.ncbi.nlm.nih.gov/pubmed/28105603
http://dx.doi.org/10.1186/s40635-017-0118-5
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