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Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats

In the liver, clock genes are proposed to drive metabolic rhythms. These gene rhythms are driven by the suprachiasmatic nucleus (SCN) mainly by food intake and via autonomic and hormonal pathways. Forced activity during the normal rest phase, induces also food intake, thus neglecting the signals of...

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Autores principales: Salgado-Delgado, Roberto C., Saderi, Nadia, Basualdo, María del Carmen, Guerrero-Vargas, Natali N., Escobar, Carolina, Buijs, Ruud M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615006/
https://www.ncbi.nlm.nih.gov/pubmed/23565183
http://dx.doi.org/10.1371/journal.pone.0060052
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author Salgado-Delgado, Roberto C.
Saderi, Nadia
Basualdo, María del Carmen
Guerrero-Vargas, Natali N.
Escobar, Carolina
Buijs, Ruud M.
author_facet Salgado-Delgado, Roberto C.
Saderi, Nadia
Basualdo, María del Carmen
Guerrero-Vargas, Natali N.
Escobar, Carolina
Buijs, Ruud M.
author_sort Salgado-Delgado, Roberto C.
collection PubMed
description In the liver, clock genes are proposed to drive metabolic rhythms. These gene rhythms are driven by the suprachiasmatic nucleus (SCN) mainly by food intake and via autonomic and hormonal pathways. Forced activity during the normal rest phase, induces also food intake, thus neglecting the signals of the SCN, leading to conflicting time signals to target tissues of the SCN. The present study explored in a rodent model of night-work the influence of food during the normal sleep period on the synchrony of gene expression between clock genes and metabolic genes in the liver. Male Wistar rats were exposed to forced activity for 8 h either during the rest phase (day) or during the active phase (night) by using a slow rotating wheel. In this shift work model food intake shifts spontaneously to the forced activity period, therefore the influence of food alone without induced activity was tested in other groups of animals that were fed ad libitum, or fed during their rest or active phase. Rats forced to be active and/or eating during their rest phase, inverted their daily peak of Per1, Bmal1 and Clock and lost the rhythm of Per2 in the liver, moreover NAMPT and metabolic genes such as Pparα lost their rhythm and thus their synchrony with clock genes. We conclude that shift work or food intake in the rest phase leads to desynchronization within the liver, characterized by misaligned temporal patterns of clock genes and metabolic genes. This may be the cause of the development of the metabolic syndrome and obesity in individuals engaged in shift work.
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spelling pubmed-36150062013-04-05 Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats Salgado-Delgado, Roberto C. Saderi, Nadia Basualdo, María del Carmen Guerrero-Vargas, Natali N. Escobar, Carolina Buijs, Ruud M. PLoS One Research Article In the liver, clock genes are proposed to drive metabolic rhythms. These gene rhythms are driven by the suprachiasmatic nucleus (SCN) mainly by food intake and via autonomic and hormonal pathways. Forced activity during the normal rest phase, induces also food intake, thus neglecting the signals of the SCN, leading to conflicting time signals to target tissues of the SCN. The present study explored in a rodent model of night-work the influence of food during the normal sleep period on the synchrony of gene expression between clock genes and metabolic genes in the liver. Male Wistar rats were exposed to forced activity for 8 h either during the rest phase (day) or during the active phase (night) by using a slow rotating wheel. In this shift work model food intake shifts spontaneously to the forced activity period, therefore the influence of food alone without induced activity was tested in other groups of animals that were fed ad libitum, or fed during their rest or active phase. Rats forced to be active and/or eating during their rest phase, inverted their daily peak of Per1, Bmal1 and Clock and lost the rhythm of Per2 in the liver, moreover NAMPT and metabolic genes such as Pparα lost their rhythm and thus their synchrony with clock genes. We conclude that shift work or food intake in the rest phase leads to desynchronization within the liver, characterized by misaligned temporal patterns of clock genes and metabolic genes. This may be the cause of the development of the metabolic syndrome and obesity in individuals engaged in shift work. Public Library of Science 2013-04-02 /pmc/articles/PMC3615006/ /pubmed/23565183 http://dx.doi.org/10.1371/journal.pone.0060052 Text en © 2013 Salgado-Delgado et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Salgado-Delgado, Roberto C.
Saderi, Nadia
Basualdo, María del Carmen
Guerrero-Vargas, Natali N.
Escobar, Carolina
Buijs, Ruud M.
Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title_full Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title_fullStr Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title_full_unstemmed Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title_short Shift Work or Food Intake during the Rest Phase Promotes Metabolic Disruption and Desynchrony of Liver Genes in Male Rats
title_sort shift work or food intake during the rest phase promotes metabolic disruption and desynchrony of liver genes in male rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615006/
https://www.ncbi.nlm.nih.gov/pubmed/23565183
http://dx.doi.org/10.1371/journal.pone.0060052
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