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Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption
Shift work and trans-time zone travel lead to insufficient sleep and numerous pathologies. Here, we examined sleep/wake dynamics during chronic exposure to environmental circadian disruption (ECD), and if chronic partial sleep loss associated with ECD influences the induction of shift-related inflam...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656961/ https://www.ncbi.nlm.nih.gov/pubmed/23696854 http://dx.doi.org/10.1371/journal.pone.0063752 |
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author | Brager, Allison J. Ehlen, J. Christopher Castanon-Cervantes, Oscar Natarajan, Divya Delisser, Patrick Davidson, Alec J. Paul, Ketema N. |
author_facet | Brager, Allison J. Ehlen, J. Christopher Castanon-Cervantes, Oscar Natarajan, Divya Delisser, Patrick Davidson, Alec J. Paul, Ketema N. |
author_sort | Brager, Allison J. |
collection | PubMed |
description | Shift work and trans-time zone travel lead to insufficient sleep and numerous pathologies. Here, we examined sleep/wake dynamics during chronic exposure to environmental circadian disruption (ECD), and if chronic partial sleep loss associated with ECD influences the induction of shift-related inflammatory disorder. Sleep and wakefulness were telemetrically recorded across three months of ECD, in which the dark-phase of a light-dark cycle was advanced weekly by 6 h. A three month regimen of ECD caused a temporary reorganization of sleep (NREM and REM) and wake processes across each week, resulting in an approximately 10% net loss of sleep each week relative to baseline levels. A separate group of mice were subjected to ECD or a regimen of imposed wakefulness (IW) aimed to mimic sleep amounts under ECD for one month. Fos-immunoreactivity (IR) was quantified in sleep-wake regulatory areas: the nucleus accumbens (NAc), basal forebrain (BF), and medial preoptic area (MnPO). To assess the inflammatory response, trunk blood was treated with lipopolysaccharide (LPS) and subsequent release of IL-6 was measured. Fos-IR was greatest in the NAc, BF, and MnPO of mice subjected to IW. The inflammatory response to LPS was elevated in mice subjected to ECD, but not mice subjected to IW. Thus, the net sleep loss that occurs under ECD is not associated with a pathological immune response. |
format | Online Article Text |
id | pubmed-3656961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36569612013-05-21 Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption Brager, Allison J. Ehlen, J. Christopher Castanon-Cervantes, Oscar Natarajan, Divya Delisser, Patrick Davidson, Alec J. Paul, Ketema N. PLoS One Research Article Shift work and trans-time zone travel lead to insufficient sleep and numerous pathologies. Here, we examined sleep/wake dynamics during chronic exposure to environmental circadian disruption (ECD), and if chronic partial sleep loss associated with ECD influences the induction of shift-related inflammatory disorder. Sleep and wakefulness were telemetrically recorded across three months of ECD, in which the dark-phase of a light-dark cycle was advanced weekly by 6 h. A three month regimen of ECD caused a temporary reorganization of sleep (NREM and REM) and wake processes across each week, resulting in an approximately 10% net loss of sleep each week relative to baseline levels. A separate group of mice were subjected to ECD or a regimen of imposed wakefulness (IW) aimed to mimic sleep amounts under ECD for one month. Fos-immunoreactivity (IR) was quantified in sleep-wake regulatory areas: the nucleus accumbens (NAc), basal forebrain (BF), and medial preoptic area (MnPO). To assess the inflammatory response, trunk blood was treated with lipopolysaccharide (LPS) and subsequent release of IL-6 was measured. Fos-IR was greatest in the NAc, BF, and MnPO of mice subjected to IW. The inflammatory response to LPS was elevated in mice subjected to ECD, but not mice subjected to IW. Thus, the net sleep loss that occurs under ECD is not associated with a pathological immune response. Public Library of Science 2013-05-17 /pmc/articles/PMC3656961/ /pubmed/23696854 http://dx.doi.org/10.1371/journal.pone.0063752 Text en © 2013 Brager et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Brager, Allison J. Ehlen, J. Christopher Castanon-Cervantes, Oscar Natarajan, Divya Delisser, Patrick Davidson, Alec J. Paul, Ketema N. Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title | Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title_full | Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title_fullStr | Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title_full_unstemmed | Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title_short | Sleep Loss and the Inflammatory Response in Mice Under Chronic Environmental Circadian Disruption |
title_sort | sleep loss and the inflammatory response in mice under chronic environmental circadian disruption |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656961/ https://www.ncbi.nlm.nih.gov/pubmed/23696854 http://dx.doi.org/10.1371/journal.pone.0063752 |
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