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 inThe journal of clinical endocrinology and metabolism Vol. 100; no. 6; pp. 2291 - 2302
Main Authors Pivovarova, Olga, Jürchott, Karsten, Rudovich, Natalia, Hornemann, Silke, Ye, Lu, Möckel, Simona, Murahovschi, Veronica, Kessler, Katharina, Seltmann, Anne-Cathrin, Maser-Gluth, Christiane, Mazuch, Jeannine, Kruse, Michael, Busjahn, Andreas, Kramer, Achim, Pfeiffer, Andreas F. H.
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 01.06.2015
Copyright by The Endocrine Society
Subjects
Online AccessGet full text
ISSN0021-972X
1945-7197
DOI10.1210/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.
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
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  surname: Rudovich
  fullname: Rudovich, Natalia
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  surname: Hornemann
  fullname: Hornemann, Silke
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  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
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  givenname: Simona
  surname: Möckel
  fullname: Möckel, Simona
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  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
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  givenname: Christiane
  surname: Maser-Gluth
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  organization: 4Institute for Pharmacology (C.M.-G.), University of Heidelberg, 69120 Heidelberg, Germany
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  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
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– 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
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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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https://www.ncbi.nlm.nih.gov/pubmed/25822100
https://www.proquest.com/docview/3164364826
Volume 100
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