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Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei

Food access restriction is associated to changes in gene expression of the circadian clock system. However, there are only a few studies investigating the effects of non-photic synchronizers, such as food entrainment, on the expression of clock genes in the central oscillators. We hypothesized that...

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Autores principales: De Araujo, Leonardo D., Roa, Silvia L., Bueno, Ana C., Coeli-Lacchini, Fernanda B., Martins, Clarissa S., Uchoa, Ernane T., Antunes-Rodrigues, Jose, Elias, Lucila L., Elias, Paula C., Moreira, Ayrton C., De Castro, Margaret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141585/
https://www.ncbi.nlm.nih.gov/pubmed/28003802
http://dx.doi.org/10.3389/fnins.2016.00567
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author De Araujo, Leonardo D.
Roa, Silvia L.
Bueno, Ana C.
Coeli-Lacchini, Fernanda B.
Martins, Clarissa S.
Uchoa, Ernane T.
Antunes-Rodrigues, Jose
Elias, Lucila L.
Elias, Paula C.
Moreira, Ayrton C.
De Castro, Margaret
author_facet De Araujo, Leonardo D.
Roa, Silvia L.
Bueno, Ana C.
Coeli-Lacchini, Fernanda B.
Martins, Clarissa S.
Uchoa, Ernane T.
Antunes-Rodrigues, Jose
Elias, Lucila L.
Elias, Paula C.
Moreira, Ayrton C.
De Castro, Margaret
author_sort De Araujo, Leonardo D.
collection PubMed
description Food access restriction is associated to changes in gene expression of the circadian clock system. However, there are only a few studies investigating the effects of non-photic synchronizers, such as food entrainment, on the expression of clock genes in the central oscillators. We hypothesized that different feeding restriction patterns could modulate the expression of clock genes in the suprachiasmatic nucleus (SCN) “master” clock and in extra-SCN oscillators such as the paraventricular (PVN) and arcuate (ARC) hypothalamic nuclei. Wistar rats were divided into four groups: Control group (CG; food available ad libitum), Restricted night-fed (RF-n; food access during 2 h at night), Restricted day-fed (RF-d; food access during 2 h at daytime), Day-fed (DF; food access during 12 h at daytime). After 21 days, rats were decapitated between ZT2-ZT3 (0800–0900 h); ZT11-ZT12 (1700–1800 h), or ZT17-18 (2300–2400 h). Plasma corticosterone was measured by radioimmunoassay (RIA). The expression of Clock, Bmal1, Per1, Per2, Per3, Cry1, Cry2, Rev-erbα, and Rorα were assessed in SCN, PVN, and ARC hypothalamic nuclei by RT-PCR and calculated by the 2([−DeltaDeltaCT(Cyclethreshold)])(2(−ΔΔCT)) method. Restricted food availability during few h led to decreased body weight in RF-n and RF-d groups compared to controls and DF group. We also observed an anticipatory corticosterone peak before food availability in RF-n and RF-d groups. Furthermore, the pattern of clock gene expression in response to RF-n, RF-d, and DF schedules was affected differently in the SCN, PVN, and ARC hypothalamic nuclei. In conclusion, the master oscillator in SCN as well as the oscillator in PVN and ARC, all brain areas involved in food intake, responds in a tissue-specific manner to feeding restriction.
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spelling pubmed-51415852016-12-21 Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei De Araujo, Leonardo D. Roa, Silvia L. Bueno, Ana C. Coeli-Lacchini, Fernanda B. Martins, Clarissa S. Uchoa, Ernane T. Antunes-Rodrigues, Jose Elias, Lucila L. Elias, Paula C. Moreira, Ayrton C. De Castro, Margaret Front Neurosci Neuroscience Food access restriction is associated to changes in gene expression of the circadian clock system. However, there are only a few studies investigating the effects of non-photic synchronizers, such as food entrainment, on the expression of clock genes in the central oscillators. We hypothesized that different feeding restriction patterns could modulate the expression of clock genes in the suprachiasmatic nucleus (SCN) “master” clock and in extra-SCN oscillators such as the paraventricular (PVN) and arcuate (ARC) hypothalamic nuclei. Wistar rats were divided into four groups: Control group (CG; food available ad libitum), Restricted night-fed (RF-n; food access during 2 h at night), Restricted day-fed (RF-d; food access during 2 h at daytime), Day-fed (DF; food access during 12 h at daytime). After 21 days, rats were decapitated between ZT2-ZT3 (0800–0900 h); ZT11-ZT12 (1700–1800 h), or ZT17-18 (2300–2400 h). Plasma corticosterone was measured by radioimmunoassay (RIA). The expression of Clock, Bmal1, Per1, Per2, Per3, Cry1, Cry2, Rev-erbα, and Rorα were assessed in SCN, PVN, and ARC hypothalamic nuclei by RT-PCR and calculated by the 2([−DeltaDeltaCT(Cyclethreshold)])(2(−ΔΔCT)) method. Restricted food availability during few h led to decreased body weight in RF-n and RF-d groups compared to controls and DF group. We also observed an anticipatory corticosterone peak before food availability in RF-n and RF-d groups. Furthermore, the pattern of clock gene expression in response to RF-n, RF-d, and DF schedules was affected differently in the SCN, PVN, and ARC hypothalamic nuclei. In conclusion, the master oscillator in SCN as well as the oscillator in PVN and ARC, all brain areas involved in food intake, responds in a tissue-specific manner to feeding restriction. Frontiers Media S.A. 2016-12-06 /pmc/articles/PMC5141585/ /pubmed/28003802 http://dx.doi.org/10.3389/fnins.2016.00567 Text en Copyright © 2016 De Araujo, Roa, Bueno, Coeli-Lacchini, Martins, Uchoa, Antunes-Rodrigues, Elias, Elias, Moreira and De Castro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
De Araujo, Leonardo D.
Roa, Silvia L.
Bueno, Ana C.
Coeli-Lacchini, Fernanda B.
Martins, Clarissa S.
Uchoa, Ernane T.
Antunes-Rodrigues, Jose
Elias, Lucila L.
Elias, Paula C.
Moreira, Ayrton C.
De Castro, Margaret
Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title_full Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title_fullStr Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title_full_unstemmed Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title_short Restricted Feeding Schedules Modulate in a Different Manner the Expression of Clock Genes in Rat Hypothalamic Nuclei
title_sort restricted feeding schedules modulate in a different manner the expression of clock genes in rat hypothalamic nuclei
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141585/
https://www.ncbi.nlm.nih.gov/pubmed/28003802
http://dx.doi.org/10.3389/fnins.2016.00567
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