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Effect of chronic ethanol consumption in female rats subjected to experimental sepsis

The objective of this research was to evaluate the interference of ethanol consumption by female rats with cytokines involved in the sepsis process and its correlation with mortality, the main outcome of sepsis. Female Wistar rats in estrus phase were evaluated in three experiments. Experiment 1 (n=...

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Autores principales: Castro, C.L., Aguiar-Nemer, A.S., Castro-Faria-Neto, H.C., Barros, F.R., Rocha, E.M.S., Silva-Fonseca, V.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935275/
https://www.ncbi.nlm.nih.gov/pubmed/24345912
http://dx.doi.org/10.1590/1414-431X20133189
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author Castro, C.L.
Aguiar-Nemer, A.S.
Castro-Faria-Neto, H.C.
Barros, F.R.
Rocha, E.M.S.
Silva-Fonseca, V.A.
author_facet Castro, C.L.
Aguiar-Nemer, A.S.
Castro-Faria-Neto, H.C.
Barros, F.R.
Rocha, E.M.S.
Silva-Fonseca, V.A.
author_sort Castro, C.L.
collection PubMed
description The objective of this research was to evaluate the interference of ethanol consumption by female rats with cytokines involved in the sepsis process and its correlation with mortality, the main outcome of sepsis. Female Wistar rats in estrus phase were evaluated in three experiments. Experiment 1 (n=40) was performed to determine survival rates. Experiment 2 (n=69) was designed for biochemical analysis, measurement of cytokine and estrogen levels before and after sepsis, and experiment 3 (n=10) was performed to evaluate bacterial growth by colony counts of peritoneal fluid. In all experiments, treated animals were exposed to a 10% ethanol/water solution (v/v) as the single drinking source, while untreated animals were given tap water. After 4 weeks, sepsis was induced in the rats by ip injection of feces. In experiment 1, mortality in ethanol-exposed animals was delayed compared with those that drank water (48 h; P=0.0001). Experiment 2 showed increased tumor necrosis factor alpha (TNF-α) and decreased interleukin-6 (IL-6) and macrophage migration inhibitory factor in septic animals exposed to ethanol compared to septic animals not exposed. Sepsis also increased TNF-α and IL-6 levels in both ethanol- and water-exposed groups. Biochemical analysis showed higher creatinine, alanine aminotransferase and aspartate aminotransferase and decreased glucose levels in septic animals that were exposed to ethanol. In experiment 3, septic animals exposed to ethanol showed decreased numbers of colony-forming units than septic animals exposed to water. These results suggest that ethanol consumption delays the mortality of female rats in estrus phase after sepsis induction. Female characteristics, most probably sex hormones, may be involved in cytokine expression.
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spelling pubmed-39352752014-03-07 Effect of chronic ethanol consumption in female rats subjected to experimental sepsis Castro, C.L. Aguiar-Nemer, A.S. Castro-Faria-Neto, H.C. Barros, F.R. Rocha, E.M.S. Silva-Fonseca, V.A. Braz J Med Biol Res Biomedical Sciences The objective of this research was to evaluate the interference of ethanol consumption by female rats with cytokines involved in the sepsis process and its correlation with mortality, the main outcome of sepsis. Female Wistar rats in estrus phase were evaluated in three experiments. Experiment 1 (n=40) was performed to determine survival rates. Experiment 2 (n=69) was designed for biochemical analysis, measurement of cytokine and estrogen levels before and after sepsis, and experiment 3 (n=10) was performed to evaluate bacterial growth by colony counts of peritoneal fluid. In all experiments, treated animals were exposed to a 10% ethanol/water solution (v/v) as the single drinking source, while untreated animals were given tap water. After 4 weeks, sepsis was induced in the rats by ip injection of feces. In experiment 1, mortality in ethanol-exposed animals was delayed compared with those that drank water (48 h; P=0.0001). Experiment 2 showed increased tumor necrosis factor alpha (TNF-α) and decreased interleukin-6 (IL-6) and macrophage migration inhibitory factor in septic animals exposed to ethanol compared to septic animals not exposed. Sepsis also increased TNF-α and IL-6 levels in both ethanol- and water-exposed groups. Biochemical analysis showed higher creatinine, alanine aminotransferase and aspartate aminotransferase and decreased glucose levels in septic animals that were exposed to ethanol. In experiment 3, septic animals exposed to ethanol showed decreased numbers of colony-forming units than septic animals exposed to water. These results suggest that ethanol consumption delays the mortality of female rats in estrus phase after sepsis induction. Female characteristics, most probably sex hormones, may be involved in cytokine expression. Associação Brasileira de Divulgação Científica 2013-12-10 /pmc/articles/PMC3935275/ /pubmed/24345912 http://dx.doi.org/10.1590/1414-431X20133189 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 Biomedical Sciences
Castro, C.L.
Aguiar-Nemer, A.S.
Castro-Faria-Neto, H.C.
Barros, F.R.
Rocha, E.M.S.
Silva-Fonseca, V.A.
Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title_full Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title_fullStr Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title_full_unstemmed Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title_short Effect of chronic ethanol consumption in female rats subjected to experimental sepsis
title_sort effect of chronic ethanol consumption in female rats subjected to experimental sepsis
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935275/
https://www.ncbi.nlm.nih.gov/pubmed/24345912
http://dx.doi.org/10.1590/1414-431X20133189
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