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Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background

Genetic and sexual factors influence the prevalence and the pathogenesis of many inflammatory disorders. In this study their relevance on the peripheral and central inflammatory status induced by a peripheral injection of lipopolysaccharide (LPS) was evaluated. BALB/c and CD-1 male and female mice w...

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Autores principales: Meneses, Gabriela, Rosetti, Marcos, Espinosa, Alejandro, Florentino, Alejandra, Bautista, Marcel, Díaz, Georgina, Olvera, Guillermo, Bárcena, Brandon, Fleury, Agnes, Adalid-Peralta, Laura, Lamoyi, Edmundo, Fragoso, Gladis, Sciutto, Edda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104912/
https://www.ncbi.nlm.nih.gov/pubmed/30133465
http://dx.doi.org/10.1371/journal.pone.0201375
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author Meneses, Gabriela
Rosetti, Marcos
Espinosa, Alejandro
Florentino, Alejandra
Bautista, Marcel
Díaz, Georgina
Olvera, Guillermo
Bárcena, Brandon
Fleury, Agnes
Adalid-Peralta, Laura
Lamoyi, Edmundo
Fragoso, Gladis
Sciutto, Edda
author_facet Meneses, Gabriela
Rosetti, Marcos
Espinosa, Alejandro
Florentino, Alejandra
Bautista, Marcel
Díaz, Georgina
Olvera, Guillermo
Bárcena, Brandon
Fleury, Agnes
Adalid-Peralta, Laura
Lamoyi, Edmundo
Fragoso, Gladis
Sciutto, Edda
author_sort Meneses, Gabriela
collection PubMed
description Genetic and sexual factors influence the prevalence and the pathogenesis of many inflammatory disorders. In this study their relevance on the peripheral and central inflammatory status induced by a peripheral injection of lipopolysaccharide (LPS) was evaluated. BALB/c and CD-1 male and female mice were intraperitoneally injected with LPS. Spleens and brains were collected 2 and 72 hours later to study the levels of IL-6, TNF-α and IL-1β. Percentage of microglia and astrocytes was determined in the cortex and hippocampus. Locomotor activity was registered before and during the 72 hours after LPS-treatment. Two hours after LPS-injection, a peripheral increase of the three cytokines was found. In brains, LPS increased TNF-α only in males with higher levels in CD-1 than BALB/c. IL-1β increased only in CD-1 males. IL-6 increased in both strains with lower levels in BALB/c females. Peripheral and central levels of cytokines decline 72 hrs after LPS-treatment whilst a significantly increase of Iba-1 expression was detected. A dramatic drop of the locomotor activity was observed immediately after LPS injection. Our results show that acute systemic administration of LPS leads to peripheral and central increase of pro-inflammatory cytokines and microglia activation, in a strain and sex dependent manner.
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spelling pubmed-61049122018-09-15 Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background Meneses, Gabriela Rosetti, Marcos Espinosa, Alejandro Florentino, Alejandra Bautista, Marcel Díaz, Georgina Olvera, Guillermo Bárcena, Brandon Fleury, Agnes Adalid-Peralta, Laura Lamoyi, Edmundo Fragoso, Gladis Sciutto, Edda PLoS One Research Article Genetic and sexual factors influence the prevalence and the pathogenesis of many inflammatory disorders. In this study their relevance on the peripheral and central inflammatory status induced by a peripheral injection of lipopolysaccharide (LPS) was evaluated. BALB/c and CD-1 male and female mice were intraperitoneally injected with LPS. Spleens and brains were collected 2 and 72 hours later to study the levels of IL-6, TNF-α and IL-1β. Percentage of microglia and astrocytes was determined in the cortex and hippocampus. Locomotor activity was registered before and during the 72 hours after LPS-treatment. Two hours after LPS-injection, a peripheral increase of the three cytokines was found. In brains, LPS increased TNF-α only in males with higher levels in CD-1 than BALB/c. IL-1β increased only in CD-1 males. IL-6 increased in both strains with lower levels in BALB/c females. Peripheral and central levels of cytokines decline 72 hrs after LPS-treatment whilst a significantly increase of Iba-1 expression was detected. A dramatic drop of the locomotor activity was observed immediately after LPS injection. Our results show that acute systemic administration of LPS leads to peripheral and central increase of pro-inflammatory cytokines and microglia activation, in a strain and sex dependent manner. Public Library of Science 2018-08-22 /pmc/articles/PMC6104912/ /pubmed/30133465 http://dx.doi.org/10.1371/journal.pone.0201375 Text en © 2018 Meneses et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Meneses, Gabriela
Rosetti, Marcos
Espinosa, Alejandro
Florentino, Alejandra
Bautista, Marcel
Díaz, Georgina
Olvera, Guillermo
Bárcena, Brandon
Fleury, Agnes
Adalid-Peralta, Laura
Lamoyi, Edmundo
Fragoso, Gladis
Sciutto, Edda
Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title_full Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title_fullStr Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title_full_unstemmed Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title_short Recovery from an acute systemic and central LPS-inflammation challenge is affected by mouse sex and genetic background
title_sort recovery from an acute systemic and central lps-inflammation challenge is affected by mouse sex and genetic background
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104912/
https://www.ncbi.nlm.nih.gov/pubmed/30133465
http://dx.doi.org/10.1371/journal.pone.0201375
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