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Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy

Although the influenza virus only infects the respiratory system, myalgias are commonly experienced during infection. In addition to a greater risk of hospitalization and death, older adults are more likely to develop disability following influenza infection; however, this relationship is understudi...

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Autores principales: Bartley, Jenna M., Pan, Sarah J., Keilich, Spencer R., Hopkins, Jacob W., Al-Naggar, Iman M., Kuchel, George A., Haynes, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925818/
https://www.ncbi.nlm.nih.gov/pubmed/26856410
http://dx.doi.org/10.18632/aging.100882
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author Bartley, Jenna M.
Pan, Sarah J.
Keilich, Spencer R.
Hopkins, Jacob W.
Al-Naggar, Iman M.
Kuchel, George A.
Haynes, Laura
author_facet Bartley, Jenna M.
Pan, Sarah J.
Keilich, Spencer R.
Hopkins, Jacob W.
Al-Naggar, Iman M.
Kuchel, George A.
Haynes, Laura
author_sort Bartley, Jenna M.
collection PubMed
description Although the influenza virus only infects the respiratory system, myalgias are commonly experienced during infection. In addition to a greater risk of hospitalization and death, older adults are more likely to develop disability following influenza infection; however, this relationship is understudied. We hypothesized that upon challenge with influenza, aging would be associated with functional impairments, as well as upregulation of skeletal muscle inflammatory and atrophy genes. Infected young and aged mice demonstrated decreased mobility and altered gait kinetics. These declines were more prominent in hind limbs and in aged mice. Skeletal muscle expression of genes involved in inflammation, as well as muscle atrophy and proteolysis, increased during influenza infection with an elevated and prolonged peak in aged mice. Infection also decreased expression of positive regulators of muscle mass and myogenesis components to a greater degree in aged mice. Gene expression correlated to influenza-induced body mass loss, although evidence did not support direct muscle infection. Overall, influenza leads to mobility impairments with induction of inflammatory and muscle degradation genes and downregulation of positive regulators of muscle. These effects are augmented and prolonged with aging, providing a molecular link between influenza infection, decreased resilience and increased risk of disability in the elderly.
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spelling pubmed-49258182016-07-01 Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy Bartley, Jenna M. Pan, Sarah J. Keilich, Spencer R. Hopkins, Jacob W. Al-Naggar, Iman M. Kuchel, George A. Haynes, Laura Aging (Albany NY) Research Paper Although the influenza virus only infects the respiratory system, myalgias are commonly experienced during infection. In addition to a greater risk of hospitalization and death, older adults are more likely to develop disability following influenza infection; however, this relationship is understudied. We hypothesized that upon challenge with influenza, aging would be associated with functional impairments, as well as upregulation of skeletal muscle inflammatory and atrophy genes. Infected young and aged mice demonstrated decreased mobility and altered gait kinetics. These declines were more prominent in hind limbs and in aged mice. Skeletal muscle expression of genes involved in inflammation, as well as muscle atrophy and proteolysis, increased during influenza infection with an elevated and prolonged peak in aged mice. Infection also decreased expression of positive regulators of muscle mass and myogenesis components to a greater degree in aged mice. Gene expression correlated to influenza-induced body mass loss, although evidence did not support direct muscle infection. Overall, influenza leads to mobility impairments with induction of inflammatory and muscle degradation genes and downregulation of positive regulators of muscle. These effects are augmented and prolonged with aging, providing a molecular link between influenza infection, decreased resilience and increased risk of disability in the elderly. Impact Journals LLC 2016-02-07 /pmc/articles/PMC4925818/ /pubmed/26856410 http://dx.doi.org/10.18632/aging.100882 Text en Copyright: © 2016 Bartley 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
Bartley, Jenna M.
Pan, Sarah J.
Keilich, Spencer R.
Hopkins, Jacob W.
Al-Naggar, Iman M.
Kuchel, George A.
Haynes, Laura
Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title_full Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title_fullStr Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title_full_unstemmed Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title_short Aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
title_sort aging augments the impact of influenza respiratory tract infection on mobility impairments, muscle-localized inflammation, and muscle atrophy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925818/
https://www.ncbi.nlm.nih.gov/pubmed/26856410
http://dx.doi.org/10.18632/aging.100882
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