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After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues

OBJECTIVE: Epidemiological studies show that shift workers are at increased risk for type 2 diabetes. As modern societies increasingly require shift work, it seems crucial to determine whether there are long‐lasting health effects of rotational shifts. METHODS: This study examined the after‐effects...

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Autores principales: de Goede, Paul, Hellings, Tom P., Coopmans, Tom V., Ritsema, Wayne I. G. R., Kalsbeek, Andries
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496197/
https://www.ncbi.nlm.nih.gov/pubmed/32475077
http://dx.doi.org/10.1002/oby.22830
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author de Goede, Paul
Hellings, Tom P.
Coopmans, Tom V.
Ritsema, Wayne I. G. R.
Kalsbeek, Andries
author_facet de Goede, Paul
Hellings, Tom P.
Coopmans, Tom V.
Ritsema, Wayne I. G. R.
Kalsbeek, Andries
author_sort de Goede, Paul
collection PubMed
description OBJECTIVE: Epidemiological studies show that shift workers are at increased risk for type 2 diabetes. As modern societies increasingly require shift work, it seems crucial to determine whether there are long‐lasting health effects of rotational shifts. METHODS: This study examined the after‐effects of 4 weeks of time‐restricted feeding (TRF) during the light period (= light‐fed) in rats, an animal model for shift work. This study also included a TRF‐dark (= dark‐fed) control group. The aligned and misaligned feeding times of light and dark feeding are associated with poor and good health outcomes, respectively. Several physiological measures were monitored continuously; blood, liver, brown adipose tissue, and soleus and gastrocnemius muscle were collected following 11 days of ad libitum (AL) feeding after ending the TRF. RESULTS: In the dark‐fed animals, the day/night differences in food intake, activity, and respiratory exchange ratio were still enhanced at the end of the experiment. Light‐fed animals displayed the smallest day/night differences for these measures, as well as for body temperature. In both the light‐ and dark‐fed animals, rhythms in plasma glucose, nonesterified fatty acids, and gene expression had not fully recovered after 11 days of AL feeding. Importantly, the effects on gene expression were both tissue and gene dependent. CONCLUSIONS: Our data indicate that rotational shift workers may have an increased risk of long‐lasting disturbed rhythms in several physiological measures after a period of shift work. Clearly, such disturbances may harm their health.
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spelling pubmed-74961972020-09-25 After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues de Goede, Paul Hellings, Tom P. Coopmans, Tom V. Ritsema, Wayne I. G. R. Kalsbeek, Andries Obesity (Silver Spring) Original Articles OBJECTIVE: Epidemiological studies show that shift workers are at increased risk for type 2 diabetes. As modern societies increasingly require shift work, it seems crucial to determine whether there are long‐lasting health effects of rotational shifts. METHODS: This study examined the after‐effects of 4 weeks of time‐restricted feeding (TRF) during the light period (= light‐fed) in rats, an animal model for shift work. This study also included a TRF‐dark (= dark‐fed) control group. The aligned and misaligned feeding times of light and dark feeding are associated with poor and good health outcomes, respectively. Several physiological measures were monitored continuously; blood, liver, brown adipose tissue, and soleus and gastrocnemius muscle were collected following 11 days of ad libitum (AL) feeding after ending the TRF. RESULTS: In the dark‐fed animals, the day/night differences in food intake, activity, and respiratory exchange ratio were still enhanced at the end of the experiment. Light‐fed animals displayed the smallest day/night differences for these measures, as well as for body temperature. In both the light‐ and dark‐fed animals, rhythms in plasma glucose, nonesterified fatty acids, and gene expression had not fully recovered after 11 days of AL feeding. Importantly, the effects on gene expression were both tissue and gene dependent. CONCLUSIONS: Our data indicate that rotational shift workers may have an increased risk of long‐lasting disturbed rhythms in several physiological measures after a period of shift work. Clearly, such disturbances may harm their health. John Wiley and Sons Inc. 2020-05-31 2020-07 /pmc/articles/PMC7496197/ /pubmed/32475077 http://dx.doi.org/10.1002/oby.22830 Text en © 2020 The Authors. Obesity published by Wiley Periodicals LLC on behalf of The Obesity Society (TOS). This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
de Goede, Paul
Hellings, Tom P.
Coopmans, Tom V.
Ritsema, Wayne I. G. R.
Kalsbeek, Andries
After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title_full After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title_fullStr After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title_full_unstemmed After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title_short After‐Effects of Time‐Restricted Feeding on Whole‐Body Metabolism and Gene Expression in Four Different Peripheral Tissues
title_sort after‐effects of time‐restricted feeding on whole‐body metabolism and gene expression in four different peripheral tissues
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496197/
https://www.ncbi.nlm.nih.gov/pubmed/32475077
http://dx.doi.org/10.1002/oby.22830
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