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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...

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Autores principales: Bano-Otalora, Beatriz, Martial, Franck, Harding, Court, Bechtold, David A., Allen, Annette E., Brown, Timothy M., Belle, Mino D. C., Lucas, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
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.
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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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