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Bright daytime light enhances circadian amplitude in a diurnal mammal
Mammalian circadian rhythms are orchestrated by a master pacemaker in the hypothalamic suprachiasmatic nuclei (SCN), which receives information about the 24 h light–dark cycle from the retina. The accepted function of this light signal is to reset circadian phase in order to ensure appropriate synch...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179182/ https://www.ncbi.nlm.nih.gov/pubmed/34031246 http://dx.doi.org/10.1073/pnas.2100094118 |
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author | Bano-Otalora, Beatriz Martial, Franck Harding, Court Bechtold, David A. Allen, Annette E. Brown, Timothy M. Belle, Mino D. C. Lucas, Robert J. |
author_facet | Bano-Otalora, Beatriz Martial, Franck Harding, Court Bechtold, David A. Allen, Annette E. Brown, Timothy M. Belle, Mino D. C. Lucas, Robert J. |
author_sort | Bano-Otalora, Beatriz |
collection | PubMed |
description | Mammalian circadian rhythms are orchestrated by a master pacemaker in the hypothalamic suprachiasmatic nuclei (SCN), which receives information about the 24 h light–dark cycle from the retina. The accepted function of this light signal is to reset circadian phase in order to ensure appropriate synchronization with the celestial day. Here, we ask whether light also impacts another key property of the circadian oscillation, its amplitude. To this end, we measured circadian rhythms in behavioral activity, body temperature, and SCN electrophysiological activity in the diurnal murid rodent Rhabdomys pumilio following stable entrainment to 12:12 light–dark cycles at four different daytime intensities (ranging from 18 to 1,900 lx melanopic equivalent daylight illuminance). R. pumilio showed strongly diurnal activity and body temperature rhythms in all conditions, but measures of rhythm robustness were positively correlated with daytime irradiance under both entrainment and subsequent free run. Whole-cell and extracellular recordings of electrophysiological activity in ex vivo SCN revealed substantial differences in electrophysiological activity between dim and bright light conditions. At lower daytime irradiance, daytime peaks in SCN spontaneous firing rate and membrane depolarization were substantially depressed, leading to an overall marked reduction in the amplitude of circadian rhythms in spontaneous activity. Our data reveal a previously unappreciated impact of daytime light intensity on SCN physiology and the amplitude of circadian rhythms and highlight the potential importance of daytime light exposure for circadian health. |
format | Online Article Text |
id | pubmed-8179182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-81791822021-06-16 Bright daytime light enhances circadian amplitude in a diurnal mammal Bano-Otalora, Beatriz Martial, Franck Harding, Court Bechtold, David A. Allen, Annette E. Brown, Timothy M. Belle, Mino D. C. Lucas, Robert J. Proc Natl Acad Sci U S A Biological Sciences Mammalian circadian rhythms are orchestrated by a master pacemaker in the hypothalamic suprachiasmatic nuclei (SCN), which receives information about the 24 h light–dark cycle from the retina. The accepted function of this light signal is to reset circadian phase in order to ensure appropriate synchronization with the celestial day. Here, we ask whether light also impacts another key property of the circadian oscillation, its amplitude. To this end, we measured circadian rhythms in behavioral activity, body temperature, and SCN electrophysiological activity in the diurnal murid rodent Rhabdomys pumilio following stable entrainment to 12:12 light–dark cycles at four different daytime intensities (ranging from 18 to 1,900 lx melanopic equivalent daylight illuminance). R. pumilio showed strongly diurnal activity and body temperature rhythms in all conditions, but measures of rhythm robustness were positively correlated with daytime irradiance under both entrainment and subsequent free run. Whole-cell and extracellular recordings of electrophysiological activity in ex vivo SCN revealed substantial differences in electrophysiological activity between dim and bright light conditions. At lower daytime irradiance, daytime peaks in SCN spontaneous firing rate and membrane depolarization were substantially depressed, leading to an overall marked reduction in the amplitude of circadian rhythms in spontaneous activity. Our data reveal a previously unappreciated impact of daytime light intensity on SCN physiology and the amplitude of circadian rhythms and highlight the potential importance of daytime light exposure for circadian health. National Academy of Sciences 2021-06-01 2021-05-24 /pmc/articles/PMC8179182/ /pubmed/34031246 http://dx.doi.org/10.1073/pnas.2100094118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Biological Sciences Bano-Otalora, Beatriz Martial, Franck Harding, Court Bechtold, David A. Allen, Annette E. Brown, Timothy M. Belle, Mino D. C. Lucas, Robert J. Bright daytime light enhances circadian amplitude in a diurnal mammal |
title | Bright daytime light enhances circadian amplitude in a diurnal mammal |
title_full | Bright daytime light enhances circadian amplitude in a diurnal mammal |
title_fullStr | Bright daytime light enhances circadian amplitude in a diurnal mammal |
title_full_unstemmed | Bright daytime light enhances circadian amplitude in a diurnal mammal |
title_short | Bright daytime light enhances circadian amplitude in a diurnal mammal |
title_sort | bright daytime light enhances circadian amplitude in a diurnal mammal |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179182/ https://www.ncbi.nlm.nih.gov/pubmed/34031246 http://dx.doi.org/10.1073/pnas.2100094118 |
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