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Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide
Obesity is associated with an increase in the prevalence and severity of infections. Genetic animal models of obesity (ob/ob and db/db mice) display altered centrally-mediated sickness behaviour in response to acute inflammatory stimuli such as lipopolysaccharide (LPS). However, the effect of diet-i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Limited
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424462/ https://www.ncbi.nlm.nih.gov/pubmed/22328591 http://dx.doi.org/10.1242/dmm.009068 |
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author | Lawrence, Catherine B. Brough, David Knight, Elysse M. |
author_facet | Lawrence, Catherine B. Brough, David Knight, Elysse M. |
author_sort | Lawrence, Catherine B. |
collection | PubMed |
description | Obesity is associated with an increase in the prevalence and severity of infections. Genetic animal models of obesity (ob/ob and db/db mice) display altered centrally-mediated sickness behaviour in response to acute inflammatory stimuli such as lipopolysaccharide (LPS). However, the effect of diet-induced obesity (DIO) on the anorectic and febrile response to LPS in mice is unknown. This study therefore determined how DIO and ob/ob mice respond to a systemic inflammatory challenge. C57BL/6 DIO and ob/ob mice, and their respective controls, were given an intraperitoneal (i.p.) injection of LPS. Compared with controls, DIO and ob/ob mice exhibited an altered febrile response to LPS (100 μg/kg) over 8 hours. LPS caused a greater and more prolonged anorexic effect in DIO compared with control mice and, in ob/ob mice, LPS induced a reduction in food intake and body weight earlier than it did in controls. These effects of LPS in obese mice were also seen after a fixed dose of LPS (5 μg). LPS (100 μg/kg) induced Fos protein expression in several brain nuclei of control mice, with fewer Fos-positive cells observed in the brains of obese mice. An altered inflammatory response to LPS was also observed in obese mice compared with controls: changes in cytokine expression and release were detected in the plasma, spleen, liver and peritoneal macrophages in obese mice. In summary, DIO and ob/ob mice displayed an altered behavioural response and cytokine release to systemic inflammatory challenge. These findings could help explain why obese humans show increased sensitivity to infections. |
format | Online Article Text |
id | pubmed-3424462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Company of Biologists Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-34244622012-09-01 Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide Lawrence, Catherine B. Brough, David Knight, Elysse M. Dis Model Mech Research Article Obesity is associated with an increase in the prevalence and severity of infections. Genetic animal models of obesity (ob/ob and db/db mice) display altered centrally-mediated sickness behaviour in response to acute inflammatory stimuli such as lipopolysaccharide (LPS). However, the effect of diet-induced obesity (DIO) on the anorectic and febrile response to LPS in mice is unknown. This study therefore determined how DIO and ob/ob mice respond to a systemic inflammatory challenge. C57BL/6 DIO and ob/ob mice, and their respective controls, were given an intraperitoneal (i.p.) injection of LPS. Compared with controls, DIO and ob/ob mice exhibited an altered febrile response to LPS (100 μg/kg) over 8 hours. LPS caused a greater and more prolonged anorexic effect in DIO compared with control mice and, in ob/ob mice, LPS induced a reduction in food intake and body weight earlier than it did in controls. These effects of LPS in obese mice were also seen after a fixed dose of LPS (5 μg). LPS (100 μg/kg) induced Fos protein expression in several brain nuclei of control mice, with fewer Fos-positive cells observed in the brains of obese mice. An altered inflammatory response to LPS was also observed in obese mice compared with controls: changes in cytokine expression and release were detected in the plasma, spleen, liver and peritoneal macrophages in obese mice. In summary, DIO and ob/ob mice displayed an altered behavioural response and cytokine release to systemic inflammatory challenge. These findings could help explain why obese humans show increased sensitivity to infections. The Company of Biologists Limited 2012-09 2012-02-10 /pmc/articles/PMC3424462/ /pubmed/22328591 http://dx.doi.org/10.1242/dmm.009068 Text en © 2012. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms. |
spellingShingle | Research Article Lawrence, Catherine B. Brough, David Knight, Elysse M. Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title | Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title_full | Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title_fullStr | Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title_full_unstemmed | Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title_short | Obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
title_sort | obese mice exhibit an altered behavioural and inflammatory response to lipopolysaccharide |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424462/ https://www.ncbi.nlm.nih.gov/pubmed/22328591 http://dx.doi.org/10.1242/dmm.009068 |
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