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The impact of hypertonic and normal saline in gut reperfusion after ischemia in rats
OBJECTIVE: We investigated the effect of two different saline solutions on the mechanisms of injury after intestinal ischemia: oxidative stress and inflammatory responses. METHODS: Wistar rats underwent transient superior mesenteric artery occlusion and were studied for 6 hours after reperfusion. Af...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Associação Brasileira de Medicina intensiva
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188464/ https://www.ncbi.nlm.nih.gov/pubmed/25295822 http://dx.doi.org/10.5935/0103-507X.20140039 |
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author | Chimabucuro, Wilson Kohama da Silva Junior, Bomfim Alves Moretti, Ana Iochabel Soares Velasco, Irineu Tadeu Rios, Ester Correia Sarmento Soriano, Francisco Garcia |
author_facet | Chimabucuro, Wilson Kohama da Silva Junior, Bomfim Alves Moretti, Ana Iochabel Soares Velasco, Irineu Tadeu Rios, Ester Correia Sarmento Soriano, Francisco Garcia |
author_sort | Chimabucuro, Wilson Kohama |
collection | PubMed |
description | OBJECTIVE: We investigated the effect of two different saline solutions on the mechanisms of injury after intestinal ischemia: oxidative stress and inflammatory responses. METHODS: Wistar rats underwent transient superior mesenteric artery occlusion and were studied for 6 hours after reperfusion. After randomization, the animals were divided into four groups: Sham; Hypertonic Saline, in which they received infusion of 4mL/kg body weight of 7.5% hypertonic saline; Saline, in which they received infusion of 33mL/kg body weight of 0.9% saline; and Non Treatment. The infusion was performed immediately prior to the reperfusion. The plasma concentrations of interleukin 6 and interleukin 10 were measured. Tissue samples (lung, liver, and intestine) were collected for malondialdehyde, myeloperoxidase, and interleukin measurements. RESULTS: The animals that received infusions (Hypertonic Saline and Saline) showed lower levels of tissue malondialdehyde, myeloperoxidase, interleukin 6, and interleukin 10 compared with the Non Treatment group. The plasma concentrations of interleukin 6 and interleukin 10 were higher in the animals treated with 7.5% hypertonic saline compared with Saline and Non Treatment groups. CONCLUSION: In this model of transient intestinal ischemia, the adequate maintenance of intravascular volume decreased oxidative stress and the synthesis of inflammatory markers. Both 7.5% Hypertonic Saline and Saline attenuated the deleterious effects observed after intestinal ischemia. |
format | Online Article Text |
id | pubmed-4188464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Associação Brasileira de Medicina intensiva |
record_format | MEDLINE/PubMed |
spelling | pubmed-41884642014-10-16 The impact of hypertonic and normal saline in gut reperfusion after ischemia in rats Chimabucuro, Wilson Kohama da Silva Junior, Bomfim Alves Moretti, Ana Iochabel Soares Velasco, Irineu Tadeu Rios, Ester Correia Sarmento Soriano, Francisco Garcia Rev Bras Ter Intensiva Original Article OBJECTIVE: We investigated the effect of two different saline solutions on the mechanisms of injury after intestinal ischemia: oxidative stress and inflammatory responses. METHODS: Wistar rats underwent transient superior mesenteric artery occlusion and were studied for 6 hours after reperfusion. After randomization, the animals were divided into four groups: Sham; Hypertonic Saline, in which they received infusion of 4mL/kg body weight of 7.5% hypertonic saline; Saline, in which they received infusion of 33mL/kg body weight of 0.9% saline; and Non Treatment. The infusion was performed immediately prior to the reperfusion. The plasma concentrations of interleukin 6 and interleukin 10 were measured. Tissue samples (lung, liver, and intestine) were collected for malondialdehyde, myeloperoxidase, and interleukin measurements. RESULTS: The animals that received infusions (Hypertonic Saline and Saline) showed lower levels of tissue malondialdehyde, myeloperoxidase, interleukin 6, and interleukin 10 compared with the Non Treatment group. The plasma concentrations of interleukin 6 and interleukin 10 were higher in the animals treated with 7.5% hypertonic saline compared with Saline and Non Treatment groups. CONCLUSION: In this model of transient intestinal ischemia, the adequate maintenance of intravascular volume decreased oxidative stress and the synthesis of inflammatory markers. Both 7.5% Hypertonic Saline and Saline attenuated the deleterious effects observed after intestinal ischemia. Associação Brasileira de Medicina intensiva 2014 /pmc/articles/PMC4188464/ /pubmed/25295822 http://dx.doi.org/10.5935/0103-507X.20140039 Text en 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 which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chimabucuro, Wilson Kohama da Silva Junior, Bomfim Alves Moretti, Ana Iochabel Soares Velasco, Irineu Tadeu Rios, Ester Correia Sarmento Soriano, Francisco Garcia The impact of hypertonic and normal saline in gut reperfusion after ischemia in rats |
title | The impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
title_full | The impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
title_fullStr | The impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
title_full_unstemmed | The impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
title_short | The impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
title_sort | impact of hypertonic and normal saline in gut reperfusion after
ischemia in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188464/ https://www.ncbi.nlm.nih.gov/pubmed/25295822 http://dx.doi.org/10.5935/0103-507X.20140039 |
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