Cargando…

Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice

Aging is an important risk factor for post-stroke infection, which accounts for a large proportion of stroke-associated mortality. Despite this, studies evaluating post-stroke infection rates in aged animal models are limited. In addition, few studies have assessed gut microbes as a potential source...

Descripción completa

Detalles Bibliográficos
Autores principales: Crapser, Joshua, Ritzel, Rodney, Verma, Rajkumar, Venna, Venugopal R., Liu, Fudong, Chauhan, Anjali, Koellhoffer, Edward, Patel, Anita, Ricker, Austin, Maas, Kendra, Graf, Joerg, McCullough, Louise D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931853/
https://www.ncbi.nlm.nih.gov/pubmed/27115295
http://dx.doi.org/10.18632/aging.100952
_version_ 1782440972716605440
author Crapser, Joshua
Ritzel, Rodney
Verma, Rajkumar
Venna, Venugopal R.
Liu, Fudong
Chauhan, Anjali
Koellhoffer, Edward
Patel, Anita
Ricker, Austin
Maas, Kendra
Graf, Joerg
McCullough, Louise D.
author_facet Crapser, Joshua
Ritzel, Rodney
Verma, Rajkumar
Venna, Venugopal R.
Liu, Fudong
Chauhan, Anjali
Koellhoffer, Edward
Patel, Anita
Ricker, Austin
Maas, Kendra
Graf, Joerg
McCullough, Louise D.
author_sort Crapser, Joshua
collection PubMed
description Aging is an important risk factor for post-stroke infection, which accounts for a large proportion of stroke-associated mortality. Despite this, studies evaluating post-stroke infection rates in aged animal models are limited. In addition, few studies have assessed gut microbes as a potential source of infection following stroke. Therefore we investigated the effects of age and the role of bacterial translocation from the gut in post-stroke infection in young (8-12 weeks) and aged (18-20 months) C57Bl/6 male mice following transient middle cerebral artery occlusion (MCAO) or sham surgery. Gut permeability was examined and peripheral organs were assessed for the presence of gut-derived bacteria following stroke. Furthermore, sickness parameters and components of innate and adaptive immunity were examined. We found that while stroke induced gut permeability and bacterial translocation in both young and aged mice, only young mice were able to resolve infection. Bacterial species seeding peripheral organs also differed between young (Escherichia) and aged (Enterobacter) mice. Consequently, aged mice developed a septic response marked by persistent and exacerbated hypothermia, weight loss, and immune dysfunction compared to young mice following stroke.
format Online
Article
Text
id pubmed-4931853
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-49318532016-07-18 Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice Crapser, Joshua Ritzel, Rodney Verma, Rajkumar Venna, Venugopal R. Liu, Fudong Chauhan, Anjali Koellhoffer, Edward Patel, Anita Ricker, Austin Maas, Kendra Graf, Joerg McCullough, Louise D. Aging (Albany NY) Research Paper Aging is an important risk factor for post-stroke infection, which accounts for a large proportion of stroke-associated mortality. Despite this, studies evaluating post-stroke infection rates in aged animal models are limited. In addition, few studies have assessed gut microbes as a potential source of infection following stroke. Therefore we investigated the effects of age and the role of bacterial translocation from the gut in post-stroke infection in young (8-12 weeks) and aged (18-20 months) C57Bl/6 male mice following transient middle cerebral artery occlusion (MCAO) or sham surgery. Gut permeability was examined and peripheral organs were assessed for the presence of gut-derived bacteria following stroke. Furthermore, sickness parameters and components of innate and adaptive immunity were examined. We found that while stroke induced gut permeability and bacterial translocation in both young and aged mice, only young mice were able to resolve infection. Bacterial species seeding peripheral organs also differed between young (Escherichia) and aged (Enterobacter) mice. Consequently, aged mice developed a septic response marked by persistent and exacerbated hypothermia, weight loss, and immune dysfunction compared to young mice following stroke. Impact Journals LLC 2016-04-25 /pmc/articles/PMC4931853/ /pubmed/27115295 http://dx.doi.org/10.18632/aging.100952 Text en Copyright: © 2016 Crapser et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Crapser, Joshua
Ritzel, Rodney
Verma, Rajkumar
Venna, Venugopal R.
Liu, Fudong
Chauhan, Anjali
Koellhoffer, Edward
Patel, Anita
Ricker, Austin
Maas, Kendra
Graf, Joerg
McCullough, Louise D.
Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title_full Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title_fullStr Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title_full_unstemmed Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title_short Ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
title_sort ischemic stroke induces gut permeability and enhances bacterial translocation leading to sepsis in aged mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931853/
https://www.ncbi.nlm.nih.gov/pubmed/27115295
http://dx.doi.org/10.18632/aging.100952
work_keys_str_mv AT crapserjoshua ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT ritzelrodney ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT vermarajkumar ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT vennavenugopalr ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT liufudong ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT chauhananjali ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT koellhofferedward ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT patelanita ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT rickeraustin ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT maaskendra ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT grafjoerg ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice
AT mcculloughlouised ischemicstrokeinducesgutpermeabilityandenhancesbacterialtranslocationleadingtosepsisinagedmice