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Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules

The circadian system is generally considered to be incapable of adjusting to rapid changes in sleep/work demands. In shiftworkers this leads to chronic circadian disruption and sleep loss, which together predict underperformance at work and negative health consequences. Two distinct experimental pro...

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Autores principales: Walbeek, Thijs J., Harrison, Elizabeth M., Soler, Robert R., Gorman, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445835/
https://www.ncbi.nlm.nih.gov/pubmed/33089177
http://dx.doi.org/10.3390/clockssleep1030032
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author Walbeek, Thijs J.
Harrison, Elizabeth M.
Soler, Robert R.
Gorman, Michael R.
author_facet Walbeek, Thijs J.
Harrison, Elizabeth M.
Soler, Robert R.
Gorman, Michael R.
author_sort Walbeek, Thijs J.
collection PubMed
description The circadian system is generally considered to be incapable of adjusting to rapid changes in sleep/work demands. In shiftworkers this leads to chronic circadian disruption and sleep loss, which together predict underperformance at work and negative health consequences. Two distinct experimental protocols have been proposed to increase circadian flexibility in rodents using dim light at night: rhythm bifurcation and T-cycle (i.e., day length) entrainment. Successful translation of such protocols to human shiftworkers could facilitate alignment of internal time with external demands. To assess entrainment flexibility following bifurcation and exposure to T-cycles, mice in Study 1 were repeatedly phase-shifted. Mice from experimental conditions rapidly phase-shifted their activity, while control mice showed expected transient misalignment. In Study 2 and 3, mice followed a several weeks-long intervention designed to model a modified DuPont or Continental shiftwork schedule, respectively. For both schedules, bifurcation and nocturnal dim lighting reduced circadian misalignment. Together, these studies demonstrate proof of concept that mammalian circadian systems can be rendered sufficiently flexible to adapt to multiple, rapidly changing shiftwork schedules. Flexible adaptation to exotic light-dark cycles likely relies on entrainment mechanisms that are distinct from traditional entrainment.
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spelling pubmed-74458352020-10-20 Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules Walbeek, Thijs J. Harrison, Elizabeth M. Soler, Robert R. Gorman, Michael R. Clocks Sleep Article The circadian system is generally considered to be incapable of adjusting to rapid changes in sleep/work demands. In shiftworkers this leads to chronic circadian disruption and sleep loss, which together predict underperformance at work and negative health consequences. Two distinct experimental protocols have been proposed to increase circadian flexibility in rodents using dim light at night: rhythm bifurcation and T-cycle (i.e., day length) entrainment. Successful translation of such protocols to human shiftworkers could facilitate alignment of internal time with external demands. To assess entrainment flexibility following bifurcation and exposure to T-cycles, mice in Study 1 were repeatedly phase-shifted. Mice from experimental conditions rapidly phase-shifted their activity, while control mice showed expected transient misalignment. In Study 2 and 3, mice followed a several weeks-long intervention designed to model a modified DuPont or Continental shiftwork schedule, respectively. For both schedules, bifurcation and nocturnal dim lighting reduced circadian misalignment. Together, these studies demonstrate proof of concept that mammalian circadian systems can be rendered sufficiently flexible to adapt to multiple, rapidly changing shiftwork schedules. Flexible adaptation to exotic light-dark cycles likely relies on entrainment mechanisms that are distinct from traditional entrainment. MDPI 2019-08-26 /pmc/articles/PMC7445835/ /pubmed/33089177 http://dx.doi.org/10.3390/clockssleep1030032 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Walbeek, Thijs J.
Harrison, Elizabeth M.
Soler, Robert R.
Gorman, Michael R.
Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title_full Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title_fullStr Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title_full_unstemmed Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title_short Enhanced Circadian Entrainment in Mice and Its Utility under Human Shiftwork Schedules
title_sort enhanced circadian entrainment in mice and its utility under human shiftwork schedules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445835/
https://www.ncbi.nlm.nih.gov/pubmed/33089177
http://dx.doi.org/10.3390/clockssleep1030032
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