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Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells

Several mechanisms are associated with brain dysfunction during sepsis; one of the most important are activation of microglia and astrocytes. Activation of glial cells induces changes in permeability of the blood-brain barrier, secretion of inflammatory cytokines, and these alterations could induce...

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Autores principales: Michels, Monique, Steckert, Amanda V., Quevedo, João, Barichello, Tatiana, Dal-Pizzol, Felipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626467/
https://www.ncbi.nlm.nih.gov/pubmed/26515197
http://dx.doi.org/10.1186/s40635-015-0066-x
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author Michels, Monique
Steckert, Amanda V.
Quevedo, João
Barichello, Tatiana
Dal-Pizzol, Felipe
author_facet Michels, Monique
Steckert, Amanda V.
Quevedo, João
Barichello, Tatiana
Dal-Pizzol, Felipe
author_sort Michels, Monique
collection PubMed
description Several mechanisms are associated with brain dysfunction during sepsis; one of the most important are activation of microglia and astrocytes. Activation of glial cells induces changes in permeability of the blood-brain barrier, secretion of inflammatory cytokines, and these alterations could induce neuronal dysfunction. Furthermore, blood-borne leukocytes can also reach the brain and participate in inflammatory response. Mechanisms involved in sepsis-associated brain dysfunction were revised here, focusing in neuroinflammation and involvement of blood-borne leukocytes and glial cells in this process.
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spelling pubmed-46264672015-11-04 Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells Michels, Monique Steckert, Amanda V. Quevedo, João Barichello, Tatiana Dal-Pizzol, Felipe Intensive Care Med Exp Review Several mechanisms are associated with brain dysfunction during sepsis; one of the most important are activation of microglia and astrocytes. Activation of glial cells induces changes in permeability of the blood-brain barrier, secretion of inflammatory cytokines, and these alterations could induce neuronal dysfunction. Furthermore, blood-borne leukocytes can also reach the brain and participate in inflammatory response. Mechanisms involved in sepsis-associated brain dysfunction were revised here, focusing in neuroinflammation and involvement of blood-borne leukocytes and glial cells in this process. Springer International Publishing 2015-10-29 /pmc/articles/PMC4626467/ /pubmed/26515197 http://dx.doi.org/10.1186/s40635-015-0066-x Text en © Michels et al. 2015 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 Review
Michels, Monique
Steckert, Amanda V.
Quevedo, João
Barichello, Tatiana
Dal-Pizzol, Felipe
Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title_full Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title_fullStr Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title_full_unstemmed Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title_short Mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
title_sort mechanisms of long-term cognitive dysfunction of sepsis: from blood-borne leukocytes to glial cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626467/
https://www.ncbi.nlm.nih.gov/pubmed/26515197
http://dx.doi.org/10.1186/s40635-015-0066-x
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