Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program

Abstract Melatonin and glucocorticoids are key hormones in determining daily rhythmicity and modulating defense responses. In nocturnal animals, corticosterone peaks at light/dark transition,while melatonin peaks at the middle of the night in both nocturnal and diurnal animals. The crosstalk between...

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Main Authors: Sanseray da Silveira Cruz-Machado, Eduardo K. Tamura, Claudia E. Carvalho-Sousa, Vanderlei Amadeu Rocha, Luciana Pinato, Pedro A. C. Fernandes, Regina P. Markus
Format: Article
Language:English
Published: Nature Publishing Group 2017-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-02286-y
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spelling doaj-426dffc13dc244318d7fcd9295dcaa862020-12-08T02:11:27ZengNature Publishing GroupScientific Reports2045-23222017-05-017111110.1038/s41598-017-02286-yDaily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional programSanseray da Silveira Cruz-Machado0Eduardo K. Tamura1Claudia E. Carvalho-Sousa2Vanderlei Amadeu Rocha3Luciana Pinato4Pedro A. C. Fernandes5Regina P. Markus6Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)São Paulo State University (UNESP)Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)Laboratory of Chronopharmacology, Department of Physiology, Institute of Biosciences, University of São Paulo (USP)Abstract Melatonin and glucocorticoids are key hormones in determining daily rhythmicity and modulating defense responses. In nocturnal animals, corticosterone peaks at light/dark transition,while melatonin peaks at the middle of the night in both nocturnal and diurnal animals. The crosstalk between adrenal and pineal glands under inflammatory conditions indicates that corticosterone potentiates nocturnal melatonin synthesis by reducing the activity of NFκB. This transcription factor, which modulates the expression of a key enzyme in melatonin synthesis, is sharply reduced at the entrance of darkness in the rat pineal gland. In this study, we established the basis for understanding the crosstalk between adrenal and pineal glands in physiological conditions. Here we show that the expression of 70 out of 84 genes implied in defense responses exhibit a sharp reduction exactly at the entrance of darkness. Mifepristone impair the changes of 13 out of 84 genes, suggesting that the rhythm of corticosterone modulates pineal phenotype, as mifepristone also reduces the expression of Aanat and the nocturnal synthesis of melatonin. Therefore, darkness-induced synthesis of the pineal hormone, besides being controlled by the central clock located in the hypothalamus, is also influencedby glucocorticoids through the regulation of NFκB transcriptional program.https://doi.org/10.1038/s41598-017-02286-y
collection DOAJ
language English
format Article
sources DOAJ
author Sanseray da Silveira Cruz-Machado
Eduardo K. Tamura
Claudia E. Carvalho-Sousa
Vanderlei Amadeu Rocha
Luciana Pinato
Pedro A. C. Fernandes
Regina P. Markus
spellingShingle Sanseray da Silveira Cruz-Machado
Eduardo K. Tamura
Claudia E. Carvalho-Sousa
Vanderlei Amadeu Rocha
Luciana Pinato
Pedro A. C. Fernandes
Regina P. Markus
Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
Scientific Reports
author_facet Sanseray da Silveira Cruz-Machado
Eduardo K. Tamura
Claudia E. Carvalho-Sousa
Vanderlei Amadeu Rocha
Luciana Pinato
Pedro A. C. Fernandes
Regina P. Markus
author_sort Sanseray da Silveira Cruz-Machado
title Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
title_short Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
title_full Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
title_fullStr Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
title_full_unstemmed Daily corticosterone rhythm modulates pineal function through NFκB-related gene transcriptional program
title_sort daily corticosterone rhythm modulates pineal function through nfκb-related gene transcriptional program
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-05-01
description Abstract Melatonin and glucocorticoids are key hormones in determining daily rhythmicity and modulating defense responses. In nocturnal animals, corticosterone peaks at light/dark transition,while melatonin peaks at the middle of the night in both nocturnal and diurnal animals. The crosstalk between adrenal and pineal glands under inflammatory conditions indicates that corticosterone potentiates nocturnal melatonin synthesis by reducing the activity of NFκB. This transcription factor, which modulates the expression of a key enzyme in melatonin synthesis, is sharply reduced at the entrance of darkness in the rat pineal gland. In this study, we established the basis for understanding the crosstalk between adrenal and pineal glands in physiological conditions. Here we show that the expression of 70 out of 84 genes implied in defense responses exhibit a sharp reduction exactly at the entrance of darkness. Mifepristone impair the changes of 13 out of 84 genes, suggesting that the rhythm of corticosterone modulates pineal phenotype, as mifepristone also reduces the expression of Aanat and the nocturnal synthesis of melatonin. Therefore, darkness-induced synthesis of the pineal hormone, besides being controlled by the central clock located in the hypothalamus, is also influencedby glucocorticoids through the regulation of NFκB transcriptional program.
url https://doi.org/10.1038/s41598-017-02286-y
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