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Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction

Caloric restriction (CR) promotes longevity in several species. Classic CR protocols often lead to chronic cycles of 2h-feeding/22h-fasting, raising the question whether calories, fasting or time of day are causal. To address this, we tested an AL control group and five CR protocols with different t...

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Autores principales: Acosta-Rodriguez, Victoria, Rijo-Ferreira, Filipa, Izumo, Mariko, Xu, Pin, Green, Carla, Takahashi, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969463/
http://dx.doi.org/10.1093/geroni/igab046.442
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author Acosta-Rodriguez, Victoria
Rijo-Ferreira, Filipa
Izumo, Mariko
Xu, Pin
Green, Carla
Takahashi, Joseph
author_facet Acosta-Rodriguez, Victoria
Rijo-Ferreira, Filipa
Izumo, Mariko
Xu, Pin
Green, Carla
Takahashi, Joseph
author_sort Acosta-Rodriguez, Victoria
collection PubMed
description Caloric restriction (CR) promotes longevity in several species. Classic CR protocols often lead to chronic cycles of 2h-feeding/22h-fasting, raising the question whether calories, fasting or time of day are causal. To address this, we tested an AL control group and five CR protocols with different timing and duration of feeding/fasting cycles. C57BL/6J male mice were subjected to 30% CR as one single meal a day at the beginning of the day or night (classical protocols with < 2h feeding, CR-day and CR-night), or smaller meals distributed for 12h (CR-day-12h and CR-night-12h), or evenly spread out throughout 24h (CR-spread) to abolish the otherwise daily feeding pattern adopted by nocturnal animals. We found that CR alone is sufficient to extend lifespan without fasting. However, the benefits are enhanced if feeding/fasting cycles are present and match their normal nocturnal activity. Circadian alignment of feeding with at least 12h fasting boosts CR-mediated increase on survival in mice, independently body weight. Aging leads to widespread upregulation of inflammation-related genes and downregulation of metabolic pathways in liver from ad lib fed mice; whereas CR at night ameliorates these aging-related changes and preserves circadian oscillations in gene expression. Overall, our results demonstrate that circadian interventions promote longevity and provide a novel perspective for elucidating mechanisms of aging.
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spelling pubmed-89694632022-04-01 Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction Acosta-Rodriguez, Victoria Rijo-Ferreira, Filipa Izumo, Mariko Xu, Pin Green, Carla Takahashi, Joseph Innov Aging Abstracts Caloric restriction (CR) promotes longevity in several species. Classic CR protocols often lead to chronic cycles of 2h-feeding/22h-fasting, raising the question whether calories, fasting or time of day are causal. To address this, we tested an AL control group and five CR protocols with different timing and duration of feeding/fasting cycles. C57BL/6J male mice were subjected to 30% CR as one single meal a day at the beginning of the day or night (classical protocols with < 2h feeding, CR-day and CR-night), or smaller meals distributed for 12h (CR-day-12h and CR-night-12h), or evenly spread out throughout 24h (CR-spread) to abolish the otherwise daily feeding pattern adopted by nocturnal animals. We found that CR alone is sufficient to extend lifespan without fasting. However, the benefits are enhanced if feeding/fasting cycles are present and match their normal nocturnal activity. Circadian alignment of feeding with at least 12h fasting boosts CR-mediated increase on survival in mice, independently body weight. Aging leads to widespread upregulation of inflammation-related genes and downregulation of metabolic pathways in liver from ad lib fed mice; whereas CR at night ameliorates these aging-related changes and preserves circadian oscillations in gene expression. Overall, our results demonstrate that circadian interventions promote longevity and provide a novel perspective for elucidating mechanisms of aging. Oxford University Press 2021-12-17 /pmc/articles/PMC8969463/ http://dx.doi.org/10.1093/geroni/igab046.442 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Acosta-Rodriguez, Victoria
Rijo-Ferreira, Filipa
Izumo, Mariko
Xu, Pin
Green, Carla
Takahashi, Joseph
Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title_full Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title_fullStr Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title_full_unstemmed Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title_short Circadian Alignment of Feeding Regulates Lifespan Extension by Caloric Restriction
title_sort circadian alignment of feeding regulates lifespan extension by caloric restriction
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969463/
http://dx.doi.org/10.1093/geroni/igab046.442
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