Changes of Dietary Fat and Carbohydrate Content Alter Central and Peripheral Clock in Humans
Context:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns influence circadian rhythms.Objective:We examined the effects of switching from a high-carbohydrate, low-fat diet to a low-carbohydrate...
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Published in | The journal of clinical endocrinology and metabolism Vol. 100; no. 6; pp. 2291 - 2302 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Oxford University Press
01.06.2015
Copyright by The Endocrine Society |
Subjects | |
Online Access | Get full text |
ISSN | 0021-972X 1945-7197 |
DOI | 10.1210/jc.2014-3868 |
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Abstract | Context:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns influence circadian rhythms.Objective:We examined the effects of switching from a high-carbohydrate, low-fat diet to a low-carbohydrate, high fat (LC/HFD) isocaloric diet on the central and peripheral circadian clocks in humans.Design:Diurnal patterns of salivary cortisol and gene expression were analyzed in blood monocytes of 29 nonobese healthy subjects before and 1 and 6 weeks after the dietary switch. For this, we established a method of rhythm prediction by 3-time point data.Results:The centrally driven cortisol rhythm showed a phase delay 1 and 6 weeks after the dietary switch to a LC/HFD as well as an amplitude increase. The dietary switch altered diurnal oscillations of core clock genes (PER1, PER2, PER3, and TEF) and inflammatory genes (CD14, CD180, NFKBIA, and IL1B). The LC/HFD also affected the expression of nonoscillating genes contributing to energy metabolism (SIRT1) and fat metabolism (ACOX3 and IDH3A). Expression of clock genes but not of salivary cortisol in monocytes tightly correlated with levels of blood lipids and with expression of metabolic and inflammatory genes.Conclusions:Our results suggest that the modulation of the dietary fat and carbohydrate content alters the function of the central and peripheral circadian clocks in humans. |
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AbstractList | Context:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns influence circadian rhythms.Objective:We examined the effects of switching from a high-carbohydrate, low-fat diet to a low-carbohydrate, high fat (LC/HFD) isocaloric diet on the central and peripheral circadian clocks in humans.Design:Diurnal patterns of salivary cortisol and gene expression were analyzed in blood monocytes of 29 nonobese healthy subjects before and 1 and 6 weeks after the dietary switch. For this, we established a method of rhythm prediction by 3-time point data.Results:The centrally driven cortisol rhythm showed a phase delay 1 and 6 weeks after the dietary switch to a LC/HFD as well as an amplitude increase. The dietary switch altered diurnal oscillations of core clock genes (PER1, PER2, PER3, and TEF) and inflammatory genes (CD14, CD180, NFKBIA, and IL1B). The LC/HFD also affected the expression of nonoscillating genes contributing to energy metabolism (SIRT1) and fat metabolism (ACOX3 and IDH3A). Expression of clock genes but not of salivary cortisol in monocytes tightly correlated with levels of blood lipids and with expression of metabolic and inflammatory genes.Conclusions:Our results suggest that the modulation of the dietary fat and carbohydrate content alters the function of the central and peripheral circadian clocks in humans. CONTEXT:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns influence circadian rhythms. OBJECTIVE:We examined the effects of switching from a high-carbohydrate, low-fat diet to a low-carbohydrate, high fat (LC/HFD) isocaloric diet on the central and peripheral circadian clocks in humans. DESIGN:Diurnal patterns of salivary cortisol and gene expression were analyzed in blood monocytes of 29 nonobese healthy subjects before and 1 and 6 weeks after the dietary switch. For this, we established a method of rhythm prediction by 3-time point data. RESULTS:The centrally driven cortisol rhythm showed a phase delay 1 and 6 weeks after the dietary switch to a LC/HFD as well as an amplitude increase. The dietary switch altered diurnal oscillations of core clock genes (PER1, PER2, PER3, and TEF) and inflammatory genes (CD14, CD180, NFKBIA, and IL1B). The LC/HFD also affected the expression of nonoscillating genes contributing to energy metabolism (SIRT1) and fat metabolism (ACOX3 and IDH3A). Expression of clock genes but not of salivary cortisol in monocytes tightly correlated with levels of blood lipids and with expression of metabolic and inflammatory genes. CONCLUSIONS:Our results suggest that the modulation of the dietary fat and carbohydrate content alters the function of the central and peripheral circadian clocks in humans. The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns influence circadian rhythms. We examined the effects of switching from a high-carbohydrate, low-fat diet to a low-carbohydrate, high fat (LC/HFD) isocaloric diet on the central and peripheral circadian clocks in humans. Diurnal patterns of salivary cortisol and gene expression were analyzed in blood monocytes of 29 nonobese healthy subjects before and 1 and 6 weeks after the dietary switch. For this, we established a method of rhythm prediction by 3-time point data. The centrally driven cortisol rhythm showed a phase delay 1 and 6 weeks after the dietary switch to a LC/HFD as well as an amplitude increase. The dietary switch altered diurnal oscillations of core clock genes (PER1, PER2, PER3, and TEF) and inflammatory genes (CD14, CD180, NFKBIA, and IL1B). The LC/HFD also affected the expression of nonoscillating genes contributing to energy metabolism (SIRT1) and fat metabolism (ACOX3 and IDH3A). Expression of clock genes but not of salivary cortisol in monocytes tightly correlated with levels of blood lipids and with expression of metabolic and inflammatory genes. Our results suggest that the modulation of the dietary fat and carbohydrate content alters the function of the central and peripheral circadian clocks in humans. |
Author | Kruse, Michael Seltmann, Anne-Cathrin Kessler, Katharina Pfeiffer, Andreas F. H. Ye, Lu Murahovschi, Veronica Rudovich, Natalia Möckel, Simona Mazuch, Jeannine Kramer, Achim Jürchott, Karsten Hornemann, Silke Pivovarova, Olga Busjahn, Andreas Maser-Gluth, Christiane |
AuthorAffiliation | Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany; Department of Endocrinology (O.P., N.R., Y.L., V.M., K.K., M.K., A.F.H.P.), Diabetes and Nutrition, Campus Benjamin Franklin, Charité University Medicine, 12203 Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies (K.J.), Charité University Medicine, 13353 Berlin, Germany; Institute for Pharmacology (C.M.-G.), University of Heidelberg, 69120 Heidelberg, Germany; Laboratory of Chronobiology (J.M., A.K.), Institute for Medical Immunology, Charité University Medicine, 10115 Berlin, Germany; and HealthTwiSt GmbH (A.B.), 13125 Berlin, Germany |
AuthorAffiliation_xml | – name: Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany; Department of Endocrinology (O.P., N.R., Y.L., V.M., K.K., M.K., A.F.H.P.), Diabetes and Nutrition, Campus Benjamin Franklin, Charité University Medicine, 12203 Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies (K.J.), Charité University Medicine, 13353 Berlin, Germany; Institute for Pharmacology (C.M.-G.), University of Heidelberg, 69120 Heidelberg, Germany; Laboratory of Chronobiology (J.M., A.K.), Institute for Medical Immunology, Charité University Medicine, 10115 Berlin, Germany; and HealthTwiSt GmbH (A.B.), 13125 Berlin, Germany |
Author_xml | – sequence: 1 givenname: Olga surname: Pivovarova fullname: Pivovarova, Olga email: olga.pivovarova@dife.de organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 2 givenname: Karsten surname: Jürchott fullname: Jürchott, Karsten organization: 3Berlin-Brandenburg Center for Regenerative Therapies (K.J.), Charité University Medicine, 13353 Berlin, Germany – sequence: 3 givenname: Natalia surname: Rudovich fullname: Rudovich, Natalia organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 4 givenname: Silke surname: Hornemann fullname: Hornemann, Silke organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 5 givenname: Lu surname: Ye fullname: Ye, Lu organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 6 givenname: Simona surname: Möckel fullname: Möckel, Simona organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 7 givenname: Veronica surname: Murahovschi fullname: Murahovschi, Veronica organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 8 givenname: Katharina surname: Kessler fullname: Kessler, Katharina organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 9 givenname: Anne-Cathrin surname: Seltmann fullname: Seltmann, Anne-Cathrin organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 10 givenname: Christiane surname: Maser-Gluth fullname: Maser-Gluth, Christiane organization: 4Institute for Pharmacology (C.M.-G.), University of Heidelberg, 69120 Heidelberg, Germany – sequence: 11 givenname: Jeannine surname: Mazuch fullname: Mazuch, Jeannine organization: 5Laboratory of Chronobiology (J.M., A.K.), Institute for Medical Immunology, Charité University Medicine, 10115 Berlin, Germany – sequence: 12 givenname: Michael surname: Kruse fullname: Kruse, Michael organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany – sequence: 13 givenname: Andreas surname: Busjahn fullname: Busjahn, Andreas organization: 6HealthTwiSt GmbH (A.B.), 13125 Berlin, Germany – sequence: 14 givenname: Achim surname: Kramer fullname: Kramer, Achim organization: 5Laboratory of Chronobiology (J.M., A.K.), Institute for Medical Immunology, Charité University Medicine, 10115 Berlin, Germany – sequence: 15 givenname: Andreas F. H. surname: Pfeiffer fullname: Pfeiffer, Andreas F. H. organization: 1Department of Clinical Nutrition (O.P., N.R., S.H., Y.L., S.M., V.M., K.K., A.-C.S., M.K., A.F.H.P.), German Institute of Human Nutrition Potsdam-Rehbruecke, 14558 Nuthetal, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25822100$$D View this record in MEDLINE/PubMed |
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Snippet | Context:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary... CONTEXT:The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary... The circadian clock coordinates numerous metabolic processes with light-dark and feeding regimens. However, in humans it is unknown whether dietary patterns... |
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SubjectTerms | Blood levels Brain - drug effects Brain - physiology Carbohydrate Metabolism - drug effects Carbohydrates CD14 antigen CD18 antigen Circadian Clocks - drug effects Circadian Clocks - genetics Circadian rhythm Circadian Rhythm - drug effects Circadian Rhythm - genetics Circadian rhythms CLOCK Proteins - genetics Cortisol Diet, Carbohydrate-Restricted Diet, Fat-Restricted Diet, High-Fat Dietary Carbohydrates - pharmacology Dietary Fats - pharmacology Diurnal Energy metabolism Fat metabolism Gene expression Gene Expression Regulation - drug effects High carbohydrate diet High fat diet Hormones Humans Hydrocortisone - metabolism Inflammation Lipid metabolism Lipid Metabolism - drug effects Low carbohydrate diet Low fat diet Metabolism Monocytes Monocytes - drug effects Monocytes - metabolism Nutrient deficiency Oils & fats Oscillations Period 1 protein Period 2 protein Period 3 protein SIRT1 protein |
Title | Changes of Dietary Fat and Carbohydrate Content Alter Central and Peripheral Clock in Humans |
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