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The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis

Circadian clock is known to adapt to environmental changes and can significantly influence cognitive and physiological functions. In this work, we report specific behavioral, cognitive, and sleep homeostatic defects in the after hours (Afh) circadian mouse mutant, which is characterized by lengthene...

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Autores principales: Maggi, Silvia, Balzani, Edoardo, Lassi, Glenda, Garcia-Garcia, Celina, Plano, Andrea, Espinoza, Stefano, Mus, Liudmila, Tinarelli, Federico, Nolan, Patrick M., Gainetdinov, Raul R., Balci, Fuat, Nieus, Thierry, Tucci, Valter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736711/
https://www.ncbi.nlm.nih.gov/pubmed/29259298
http://dx.doi.org/10.1038/s41598-017-18130-2
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author Maggi, Silvia
Balzani, Edoardo
Lassi, Glenda
Garcia-Garcia, Celina
Plano, Andrea
Espinoza, Stefano
Mus, Liudmila
Tinarelli, Federico
Nolan, Patrick M.
Gainetdinov, Raul R.
Balci, Fuat
Nieus, Thierry
Tucci, Valter
author_facet Maggi, Silvia
Balzani, Edoardo
Lassi, Glenda
Garcia-Garcia, Celina
Plano, Andrea
Espinoza, Stefano
Mus, Liudmila
Tinarelli, Federico
Nolan, Patrick M.
Gainetdinov, Raul R.
Balci, Fuat
Nieus, Thierry
Tucci, Valter
author_sort Maggi, Silvia
collection PubMed
description Circadian clock is known to adapt to environmental changes and can significantly influence cognitive and physiological functions. In this work, we report specific behavioral, cognitive, and sleep homeostatic defects in the after hours (Afh) circadian mouse mutant, which is characterized by lengthened circadian period. We found that the circadian timing irregularities in Afh mice resulted in higher interval timing uncertainty and suboptimal decisions due to incapability of processing probabilities. Our phenotypic observations further suggested that Afh mutants failed to exhibit the necessary phenotypic plasticity for adapting to temporal changes at multiple time scales (seconds-to-minutes to circadian). These behavioral effects of Afh mutation were complemented by the specific disruption of the Per/Cry circadian regulatory complex in brain regions that govern food anticipatory behaviors, sleep, and timing. We derive statistical predictions, which indicate that circadian clock and sleep are complementary processes in controlling behavioral/cognitive performance during 24 hrs. The results of this study have pivotal implications for understanding how the circadian clock modulates sleep and behavior.
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spelling pubmed-57367112017-12-21 The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis Maggi, Silvia Balzani, Edoardo Lassi, Glenda Garcia-Garcia, Celina Plano, Andrea Espinoza, Stefano Mus, Liudmila Tinarelli, Federico Nolan, Patrick M. Gainetdinov, Raul R. Balci, Fuat Nieus, Thierry Tucci, Valter Sci Rep Article Circadian clock is known to adapt to environmental changes and can significantly influence cognitive and physiological functions. In this work, we report specific behavioral, cognitive, and sleep homeostatic defects in the after hours (Afh) circadian mouse mutant, which is characterized by lengthened circadian period. We found that the circadian timing irregularities in Afh mice resulted in higher interval timing uncertainty and suboptimal decisions due to incapability of processing probabilities. Our phenotypic observations further suggested that Afh mutants failed to exhibit the necessary phenotypic plasticity for adapting to temporal changes at multiple time scales (seconds-to-minutes to circadian). These behavioral effects of Afh mutation were complemented by the specific disruption of the Per/Cry circadian regulatory complex in brain regions that govern food anticipatory behaviors, sleep, and timing. We derive statistical predictions, which indicate that circadian clock and sleep are complementary processes in controlling behavioral/cognitive performance during 24 hrs. The results of this study have pivotal implications for understanding how the circadian clock modulates sleep and behavior. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736711/ /pubmed/29259298 http://dx.doi.org/10.1038/s41598-017-18130-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Maggi, Silvia
Balzani, Edoardo
Lassi, Glenda
Garcia-Garcia, Celina
Plano, Andrea
Espinoza, Stefano
Mus, Liudmila
Tinarelli, Federico
Nolan, Patrick M.
Gainetdinov, Raul R.
Balci, Fuat
Nieus, Thierry
Tucci, Valter
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title_full The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title_fullStr The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title_full_unstemmed The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title_short The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
title_sort after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736711/
https://www.ncbi.nlm.nih.gov/pubmed/29259298
http://dx.doi.org/10.1038/s41598-017-18130-2
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