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LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats
Behavioral symptoms of sickness, such as fever and motor activity are a coordinated set of changes that develop during infection. The aim of study was to compare the sickness behaviour (SB) in healthy old and young rats treated with pyrogenic dose of endotoxin and to check their glutathione level. B...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933742/ https://www.ncbi.nlm.nih.gov/pubmed/26829940 http://dx.doi.org/10.1007/s10522-016-9636-x |
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author | Wrotek, Sylwia Jędrzejewski, Tomasz Nowakowska, Anna Kozak, Wiesław |
author_facet | Wrotek, Sylwia Jędrzejewski, Tomasz Nowakowska, Anna Kozak, Wiesław |
author_sort | Wrotek, Sylwia |
collection | PubMed |
description | Behavioral symptoms of sickness, such as fever and motor activity are a coordinated set of changes that develop during infection. The aim of study was to compare the sickness behaviour (SB) in healthy old and young rats treated with pyrogenic dose of endotoxin and to check their glutathione level. Before experimentation male Wistar rats were selected according to standard body mass, motor activity, and white blood cells count. Intraperitoneal injection of lipopolysaccharide (LPS) from E. coli was used to provoke SB. The level of liver glutathione, interleukin (IL) -6, deep body temperature (Tb) and motor activity were measured. Glutathione level in old and young rats did not differ significantly. In both young and old rats LPS administration provoked fever (the mean value of Tb was 38.06 ± 0.01 °C in old rats, and 38.19 ± 0.06 °C in young rats). LPS injection affected night-time activity in both groups (12 h averages were 1.56 ± 0.40 counts in old LPS-treated rats vs 2.74 ± 0.53 counts in not-treated old rats and 3.44 ± 0.60 counts for young LPS-treated vs 4.28 ± 0.57 counts for young not-treated rats). The injection of LPS provoked an elevation of plasma IL-6 concentration (from values below the lowest detectable standard in not-treated groups of animals to 6322.82 ± 537.00 pg/mL in old LPS-treated rats and 7415.62 ± 451.88 pg/mL in young LPS-treated rats). Based on these data, we conclude that good health of aged rats prevents decrease in the glutathione level. Old rats are still able to develop SB in response to pyrogenic dose of LPS, although its components have changed pattern compared to young animals. |
format | Online Article Text |
id | pubmed-4933742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-49337422016-07-18 LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats Wrotek, Sylwia Jędrzejewski, Tomasz Nowakowska, Anna Kozak, Wiesław Biogerontology Research Article Behavioral symptoms of sickness, such as fever and motor activity are a coordinated set of changes that develop during infection. The aim of study was to compare the sickness behaviour (SB) in healthy old and young rats treated with pyrogenic dose of endotoxin and to check their glutathione level. Before experimentation male Wistar rats were selected according to standard body mass, motor activity, and white blood cells count. Intraperitoneal injection of lipopolysaccharide (LPS) from E. coli was used to provoke SB. The level of liver glutathione, interleukin (IL) -6, deep body temperature (Tb) and motor activity were measured. Glutathione level in old and young rats did not differ significantly. In both young and old rats LPS administration provoked fever (the mean value of Tb was 38.06 ± 0.01 °C in old rats, and 38.19 ± 0.06 °C in young rats). LPS injection affected night-time activity in both groups (12 h averages were 1.56 ± 0.40 counts in old LPS-treated rats vs 2.74 ± 0.53 counts in not-treated old rats and 3.44 ± 0.60 counts for young LPS-treated vs 4.28 ± 0.57 counts for young not-treated rats). The injection of LPS provoked an elevation of plasma IL-6 concentration (from values below the lowest detectable standard in not-treated groups of animals to 6322.82 ± 537.00 pg/mL in old LPS-treated rats and 7415.62 ± 451.88 pg/mL in young LPS-treated rats). Based on these data, we conclude that good health of aged rats prevents decrease in the glutathione level. Old rats are still able to develop SB in response to pyrogenic dose of LPS, although its components have changed pattern compared to young animals. Springer Netherlands 2016-02-01 2016 /pmc/articles/PMC4933742/ /pubmed/26829940 http://dx.doi.org/10.1007/s10522-016-9636-x Text en © The Author(s) 2016 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 Article Wrotek, Sylwia Jędrzejewski, Tomasz Nowakowska, Anna Kozak, Wiesław LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title | LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title_full | LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title_fullStr | LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title_full_unstemmed | LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title_short | LPS alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
title_sort | lps alters pattern of sickness behavior but does not affect glutathione level in aged male rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4933742/ https://www.ncbi.nlm.nih.gov/pubmed/26829940 http://dx.doi.org/10.1007/s10522-016-9636-x |
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