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Differentiating external zeitgeber impact on peripheral circadian clock resetting
Circadian clocks regulate physiological functions, including energy metabolism, along the 24-hour day cycle. The mammalian clock system is organized in a hierarchical manner with a coordinating pacemaker residing in the hypothalamic suprachiasmatic nucleus (SCN). The SCN clock is reset primarily by...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934673/ https://www.ncbi.nlm.nih.gov/pubmed/31882641 http://dx.doi.org/10.1038/s41598-019-56323-z |
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author | Heyde, Isabel Oster, Henrik |
author_facet | Heyde, Isabel Oster, Henrik |
author_sort | Heyde, Isabel |
collection | PubMed |
description | Circadian clocks regulate physiological functions, including energy metabolism, along the 24-hour day cycle. The mammalian clock system is organized in a hierarchical manner with a coordinating pacemaker residing in the hypothalamic suprachiasmatic nucleus (SCN). The SCN clock is reset primarily by the external light-dark cycle while other zeitgebers such as the timing of food intake are potent synchronizers of many peripheral tissue clocks. Under conflicting zeitgeber conditions, e.g. during shift work, phase synchrony across the clock network is disrupted promoting the development of metabolic disorders. We established a zeitgeber desynchrony (ZD) paradigm to quantify the differential contributions of the two main zeitgebers, light and food, to the resetting of specific tissue clocks and the effect on metabolic homeostasis in mice. Under 28-hour light-dark and 24-hour feeding-fasting conditions SCN and peripheral clock, as well as activity and hormonal rhythms showed specific periodicities aligning in-between those of the two zeitgebers. During ZD, metabolic homeostasis was cyclic with mice gaining weight under synchronous and losing weight under conflicting zeitgeber conditions. In summary, our study establishes an experimental paradigm to compare zeitgeber input in vivo and study the physiological consequences of chronodisruption. |
format | Online Article Text |
id | pubmed-6934673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69346732019-12-30 Differentiating external zeitgeber impact on peripheral circadian clock resetting Heyde, Isabel Oster, Henrik Sci Rep Article Circadian clocks regulate physiological functions, including energy metabolism, along the 24-hour day cycle. The mammalian clock system is organized in a hierarchical manner with a coordinating pacemaker residing in the hypothalamic suprachiasmatic nucleus (SCN). The SCN clock is reset primarily by the external light-dark cycle while other zeitgebers such as the timing of food intake are potent synchronizers of many peripheral tissue clocks. Under conflicting zeitgeber conditions, e.g. during shift work, phase synchrony across the clock network is disrupted promoting the development of metabolic disorders. We established a zeitgeber desynchrony (ZD) paradigm to quantify the differential contributions of the two main zeitgebers, light and food, to the resetting of specific tissue clocks and the effect on metabolic homeostasis in mice. Under 28-hour light-dark and 24-hour feeding-fasting conditions SCN and peripheral clock, as well as activity and hormonal rhythms showed specific periodicities aligning in-between those of the two zeitgebers. During ZD, metabolic homeostasis was cyclic with mice gaining weight under synchronous and losing weight under conflicting zeitgeber conditions. In summary, our study establishes an experimental paradigm to compare zeitgeber input in vivo and study the physiological consequences of chronodisruption. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934673/ /pubmed/31882641 http://dx.doi.org/10.1038/s41598-019-56323-z Text en © The Author(s) 2019 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 Heyde, Isabel Oster, Henrik Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title | Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title_full | Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title_fullStr | Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title_full_unstemmed | Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title_short | Differentiating external zeitgeber impact on peripheral circadian clock resetting |
title_sort | differentiating external zeitgeber impact on peripheral circadian clock resetting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934673/ https://www.ncbi.nlm.nih.gov/pubmed/31882641 http://dx.doi.org/10.1038/s41598-019-56323-z |
work_keys_str_mv | AT heydeisabel differentiatingexternalzeitgeberimpactonperipheralcircadianclockresetting AT osterhenrik differentiatingexternalzeitgeberimpactonperipheralcircadianclockresetting |