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Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis

Although in-hospital mortality rates for sepsis have decreased, survivors often experience lasting physical and cognitive deficits. Moreover, older adults are more vulnerable to long-term complications associated with sepsis. We employed a murine model to examine the influence of age and sex on the...

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Autores principales: Barter, Jolie, Kumar, Ashok, Stortz, Julie A., Hollen, McKenzie, Nacionales, Dina, Efron, Philip A., Moldawer, Lyle L., Foster, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834928/
https://www.ncbi.nlm.nih.gov/pubmed/31278440
http://dx.doi.org/10.1007/s12035-019-01681-y
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author Barter, Jolie
Kumar, Ashok
Stortz, Julie A.
Hollen, McKenzie
Nacionales, Dina
Efron, Philip A.
Moldawer, Lyle L.
Foster, Thomas C.
author_facet Barter, Jolie
Kumar, Ashok
Stortz, Julie A.
Hollen, McKenzie
Nacionales, Dina
Efron, Philip A.
Moldawer, Lyle L.
Foster, Thomas C.
author_sort Barter, Jolie
collection PubMed
description Although in-hospital mortality rates for sepsis have decreased, survivors often experience lasting physical and cognitive deficits. Moreover, older adults are more vulnerable to long-term complications associated with sepsis. We employed a murine model to examine the influence of age and sex on the brain’s response and recovery following sepsis. Young (~ 4 months) and old (~ 20 months) mice (C57BL/6) of both sexes underwent cecal ligation and puncture (CLP) with restraint stress. The hippocampal transcriptome was examined in age- and sex-matched controls at 1 and 4 days post-CLP. In general, immune- and stress-related genes increased, while neuronal, synaptic, and glial genes decreased 1 day after CLP-induced sepsis. However, specific age and sex differences were observed for the initial responsiveness to sepsis as well as the rate of recovery examined on day 4. Young females exhibited a muted transcriptional response relative to young males and old females. Old females exhibited a robust shift in gene transcription on day 1, and while most genes recovered, genes linked to neurogenesis and myelination continued to be downregulated by day 4. In contrast, old males exhibited a more delayed or prolonged response to sepsis, such that neuronal and synaptic genes continued to decrease while immune response genes continued to increase on day 4. These results suggest that aging is associated with delayed recovery from sepsis, which is particularly evident in males. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-019-01681-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-68349282019-11-20 Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis Barter, Jolie Kumar, Ashok Stortz, Julie A. Hollen, McKenzie Nacionales, Dina Efron, Philip A. Moldawer, Lyle L. Foster, Thomas C. Mol Neurobiol Article Although in-hospital mortality rates for sepsis have decreased, survivors often experience lasting physical and cognitive deficits. Moreover, older adults are more vulnerable to long-term complications associated with sepsis. We employed a murine model to examine the influence of age and sex on the brain’s response and recovery following sepsis. Young (~ 4 months) and old (~ 20 months) mice (C57BL/6) of both sexes underwent cecal ligation and puncture (CLP) with restraint stress. The hippocampal transcriptome was examined in age- and sex-matched controls at 1 and 4 days post-CLP. In general, immune- and stress-related genes increased, while neuronal, synaptic, and glial genes decreased 1 day after CLP-induced sepsis. However, specific age and sex differences were observed for the initial responsiveness to sepsis as well as the rate of recovery examined on day 4. Young females exhibited a muted transcriptional response relative to young males and old females. Old females exhibited a robust shift in gene transcription on day 1, and while most genes recovered, genes linked to neurogenesis and myelination continued to be downregulated by day 4. In contrast, old males exhibited a more delayed or prolonged response to sepsis, such that neuronal and synaptic genes continued to decrease while immune response genes continued to increase on day 4. These results suggest that aging is associated with delayed recovery from sepsis, which is particularly evident in males. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-019-01681-y) contains supplementary material, which is available to authorized users. Springer US 2019-07-05 2019 /pmc/articles/PMC6834928/ /pubmed/31278440 http://dx.doi.org/10.1007/s12035-019-01681-y Text en © The Author(s) 2019 Open Access This 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 Article
Barter, Jolie
Kumar, Ashok
Stortz, Julie A.
Hollen, McKenzie
Nacionales, Dina
Efron, Philip A.
Moldawer, Lyle L.
Foster, Thomas C.
Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title_full Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title_fullStr Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title_full_unstemmed Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title_short Age and Sex Influence the Hippocampal Response and Recovery Following Sepsis
title_sort age and sex influence the hippocampal response and recovery following sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834928/
https://www.ncbi.nlm.nih.gov/pubmed/31278440
http://dx.doi.org/10.1007/s12035-019-01681-y
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