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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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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. |
format | Online Article Text |
id | pubmed-6834928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
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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