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Hypertonic saline solution reduces the inflammatory response in endotoxemic rats
OBJECTIVE: Volume replacement in septic patients improves hemodynamic stability. This effect can reduce the inflammatory response. The objective of this study was to evaluate the effect of 7.5% hypertonic saline solution versus 0.9% normal saline solution for volume replacement during an inflammator...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521811/ https://www.ncbi.nlm.nih.gov/pubmed/23295602 http://dx.doi.org/10.6061/clinics/2012(12)18 |
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author | Theobaldo, Mariana Cardillo Barbeiro, Hermes Vieira Barbeiro, Denise Frediani Petroni, Ricardo Soriano, Francisco Garcia |
author_facet | Theobaldo, Mariana Cardillo Barbeiro, Hermes Vieira Barbeiro, Denise Frediani Petroni, Ricardo Soriano, Francisco Garcia |
author_sort | Theobaldo, Mariana Cardillo |
collection | PubMed |
description | OBJECTIVE: Volume replacement in septic patients improves hemodynamic stability. This effect can reduce the inflammatory response. The objective of this study was to evaluate the effect of 7.5% hypertonic saline solution versus 0.9% normal saline solution for volume replacement during an inflammatory response in endotoxemic rats. METHODS: We measured cytokines (serum and gut), nitrite, and lipid peroxidation (TBARS) as indicators of oxidative stress in the gut. Rats were divided into four groups: control group (C) that did not receive lipopolysaccharide; lipopolysaccharide injection without treatment (LPS); lipopolysaccharide injection with saline treatment (LPS +S); and lipopolysaccharide injection with hypertonic saline treatment (LPS +H). Serum and intestine were collected. Measurements were taken at 1.5, 8, and 24 h after lipopolysaccharide administration. RESULTS: Of the four groups, the LPS +H group had the highest survival rate. Hypertonic saline solution treatment led to lower levels of IL-6, IL-10, nitric oxide, and thiobarbituric acid reactive substances compared to 0.9% normal saline. In addition, hypertonic saline treatment resulted in a lower mortality compared to 0.9% normal saline treatment in endotoxemic rats. Volume replacement reduced levels of inflammatory mediators in the plasma and gut. CONCLUSION: Hypertonic saline treatment reduced mortality and lowered levels of inflammatory mediators in endotoxemic rats. Hypertonic saline also has the advantage of requiring less volume replacement. |
format | Online Article Text |
id | pubmed-3521811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-35218112012-12-17 Hypertonic saline solution reduces the inflammatory response in endotoxemic rats Theobaldo, Mariana Cardillo Barbeiro, Hermes Vieira Barbeiro, Denise Frediani Petroni, Ricardo Soriano, Francisco Garcia Clinics (Sao Paulo) Basic Research OBJECTIVE: Volume replacement in septic patients improves hemodynamic stability. This effect can reduce the inflammatory response. The objective of this study was to evaluate the effect of 7.5% hypertonic saline solution versus 0.9% normal saline solution for volume replacement during an inflammatory response in endotoxemic rats. METHODS: We measured cytokines (serum and gut), nitrite, and lipid peroxidation (TBARS) as indicators of oxidative stress in the gut. Rats were divided into four groups: control group (C) that did not receive lipopolysaccharide; lipopolysaccharide injection without treatment (LPS); lipopolysaccharide injection with saline treatment (LPS +S); and lipopolysaccharide injection with hypertonic saline treatment (LPS +H). Serum and intestine were collected. Measurements were taken at 1.5, 8, and 24 h after lipopolysaccharide administration. RESULTS: Of the four groups, the LPS +H group had the highest survival rate. Hypertonic saline solution treatment led to lower levels of IL-6, IL-10, nitric oxide, and thiobarbituric acid reactive substances compared to 0.9% normal saline. In addition, hypertonic saline treatment resulted in a lower mortality compared to 0.9% normal saline treatment in endotoxemic rats. Volume replacement reduced levels of inflammatory mediators in the plasma and gut. CONCLUSION: Hypertonic saline treatment reduced mortality and lowered levels of inflammatory mediators in endotoxemic rats. Hypertonic saline also has the advantage of requiring less volume replacement. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012-12 /pmc/articles/PMC3521811/ /pubmed/23295602 http://dx.doi.org/10.6061/clinics/2012(12)18 Text en Copyright © 2012 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Research Theobaldo, Mariana Cardillo Barbeiro, Hermes Vieira Barbeiro, Denise Frediani Petroni, Ricardo Soriano, Francisco Garcia Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title | Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title_full | Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title_fullStr | Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title_full_unstemmed | Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title_short | Hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
title_sort | hypertonic saline solution reduces the inflammatory response in endotoxemic rats |
topic | Basic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521811/ https://www.ncbi.nlm.nih.gov/pubmed/23295602 http://dx.doi.org/10.6061/clinics/2012(12)18 |
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