Eating breakfast and avoiding late-evening snacking sustains lipid oxidation
Circadian (daily) regulation of metabolic pathways implies that food may be metabolized differentially over the daily cycle. To test that hypothesis, we monitored the metabolism of older subjects in a whole-room respiratory chamber over two separate 56-h sessions in a random crossover design. In one...
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Published in | PLoS biology Vol. 18; no. 2; p. e3000622 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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27.02.2020
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Abstract | Circadian (daily) regulation of metabolic pathways implies that food may be metabolized differentially over the daily cycle. To test that hypothesis, we monitored the metabolism of older subjects in a whole-room respiratory chamber over two separate 56-h sessions in a random crossover design. In one session, one of the 3 daily meals was presented as breakfast, whereas in the other session, a nutritionally equivalent meal was presented as a late-evening snack. The duration of the overnight fast was the same for both sessions. Whereas the two sessions did not differ in overall energy expenditure, the respiratory exchange ratio (RER) was different during sleep between the two sessions. Unexpectedly, this difference in RER due to daily meal timing was not due to daily differences in physical activity, sleep disruption, or core body temperature (CBT). Rather, we found that the daily timing of nutrient availability coupled with daily/circadian control of metabolism drives a switch in substrate preference such that the late-evening Snack Session resulted in significantly lower lipid oxidation (LO) compared to the Breakfast Session. Therefore, the timing of meals during the day/night cycle affects how ingested food is oxidized or stored in humans, with important implications for optimal eating habits. |
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AbstractList | Circadian (daily) regulation of metabolic pathways implies that food may be metabolized differentially over the daily cycle. To test that hypothesis, we monitored the metabolism of older subjects in a whole-room respiratory chamber over two separate 56-h sessions in a random crossover design. In one session, one of the 3 daily meals was presented as breakfast, whereas in the other session, a nutritionally equivalent meal was presented as a late-evening snack. The duration of the overnight fast was the same for both sessions. Whereas the two sessions did not differ in overall energy expenditure, the respiratory exchange ratio (RER) was different during sleep between the two sessions. Unexpectedly, this difference in RER due to daily meal timing was not due to daily differences in physical activity, sleep disruption, or core body temperature (CBT). Rather, we found that the daily timing of nutrient availability coupled with daily/circadian control of metabolism drives a switch in substrate preference such that the late-evening Snack Session resulted in significantly lower lipid oxidation (LO) compared to the Breakfast Session. Therefore, the timing of meals during the day/night cycle affects how ingested food is oxidized or stored in humans, with important implications for optimal eating habits. Circadian (daily) regulation of metabolic pathways implies that food may be metabolized differentially over the daily cycle. To test that hypothesis, we monitored the metabolism of older subjects in a whole-room respiratory chamber over two separate 56-h sessions in a random crossover design. In one session, one of the 3 daily meals was presented as breakfast, whereas in the other session, a nutritionally equivalent meal was presented as a late-evening snack. The duration of the overnight fast was the same for both sessions. Whereas the two sessions did not differ in overall energy expenditure, the respiratory exchange ratio (RER) was different during sleep between the two sessions. Unexpectedly, this difference in RER due to daily meal timing was not due to daily differences in physical activity, sleep disruption, or core body temperature (CBT). Rather, we found that the daily timing of nutrient availability coupled with daily/circadian control of metabolism drives a switch in substrate preference such that the late-evening Snack Session resulted in significantly lower lipid oxidation (LO) compared to the Breakfast Session. Therefore, the timing of meals during the day/night cycle affects how ingested food is oxidized or stored in humans, with important implications for optimal eating habits.Circadian (daily) regulation of metabolic pathways implies that food may be metabolized differentially over the daily cycle. To test that hypothesis, we monitored the metabolism of older subjects in a whole-room respiratory chamber over two separate 56-h sessions in a random crossover design. In one session, one of the 3 daily meals was presented as breakfast, whereas in the other session, a nutritionally equivalent meal was presented as a late-evening snack. The duration of the overnight fast was the same for both sessions. Whereas the two sessions did not differ in overall energy expenditure, the respiratory exchange ratio (RER) was different during sleep between the two sessions. Unexpectedly, this difference in RER due to daily meal timing was not due to daily differences in physical activity, sleep disruption, or core body temperature (CBT). Rather, we found that the daily timing of nutrient availability coupled with daily/circadian control of metabolism drives a switch in substrate preference such that the late-evening Snack Session resulted in significantly lower lipid oxidation (LO) compared to the Breakfast Session. Therefore, the timing of meals during the day/night cycle affects how ingested food is oxidized or stored in humans, with important implications for optimal eating habits. |
Audience | Academic |
Author | Page, Terry Hughey, Jacob J. Johnson, Carl Hirschie Buchowski, Maciej McGuinness, Owen P. Chen, Heidi Powers, James Kelly, Kevin Parsons |
AuthorAffiliation | 7 Tennessee Valley Healthcare System Geriatric Research, Education, and Clinical Center, Nashville, Tennessee, United States of America Charité - Universitätsmedizin Berlin, GERMANY 1 Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America 6 Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America 4 Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America 5 Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America 3 Division of Gastroenterology, Hepatology, & Nutrition, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America 2 Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America |
AuthorAffiliation_xml | – name: 5 Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America – name: 3 Division of Gastroenterology, Hepatology, & Nutrition, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America – name: 2 Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America – name: 4 Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America – name: 7 Tennessee Valley Healthcare System Geriatric Research, Education, and Clinical Center, Nashville, Tennessee, United States of America – name: Charité - Universitätsmedizin Berlin, GERMANY – name: 6 Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America – name: 1 Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America |
Author_xml | – sequence: 1 givenname: Kevin Parsons surname: Kelly fullname: Kelly, Kevin Parsons – sequence: 2 givenname: Owen P. orcidid: 0000-0002-1778-3203 surname: McGuinness fullname: McGuinness, Owen P. – sequence: 3 givenname: Maciej surname: Buchowski fullname: Buchowski, Maciej – sequence: 4 givenname: Jacob J. orcidid: 0000-0002-1558-6089 surname: Hughey fullname: Hughey, Jacob J. – sequence: 5 givenname: Heidi surname: Chen fullname: Chen, Heidi – sequence: 6 givenname: James surname: Powers fullname: Powers, James – sequence: 7 givenname: Terry surname: Page fullname: Page, Terry – sequence: 8 givenname: Carl Hirschie orcidid: 0000-0003-2878-3193 surname: Johnson fullname: Johnson, Carl Hirschie |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32108181$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2020 Public Library of Science 2020 Kelly et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2020 Kelly et al 2020 Kelly et al |
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SubjectTerms | Biological clocks Biology and Life Sciences Biophysics Body Mass Index Body temperature Breakfast Carbohydrate Metabolism - physiology Carbohydrates Circadian rhythm Circadian Rhythm - physiology Circadian rhythms Cross-Over Studies Crossovers Disruption Eating Eating behavior Energy Energy expenditure Evening Exercise Feeding Behavior - physiology Female Food Food habits Gene expression Human subjects Humans Industrialized nations Lipid Metabolism - physiology Lipid peroxidation Lipids Male Meals Meals - physiology Medical research Medicine and Health Sciences Metabolic pathways Metabolism Middle Aged Nutrient availability Nutrition research Obesity Oxidation Oxidation-Reduction Oxidation-reduction reaction Physical activity Physical Sciences Physiological aspects Physiology Pulmonary Gas Exchange - physiology Research and Analysis Methods Short Reports Sleep Sleep - physiology Snacks Substrate preferences Substrates Type 2 diabetes Weight control |
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Title | Eating breakfast and avoiding late-evening snacking sustains lipid oxidation |
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