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Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters
Nocturnal secretion of melatonin from the pineal gland may affect central and peripheral timing, in addition to its well-known involvement in the control of seasonal physiology. The Syrian hamster is a photoperiodic species, which displays gonadal atrophy and increased adiposity when adapted to shor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444759/ https://www.ncbi.nlm.nih.gov/pubmed/26074760 http://dx.doi.org/10.3389/fnins.2015.00190 |
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author | Chakir, Ibtissam Dumont, Stéphanie Pévet, Paul Ouarour, Ali Challet, Etienne Vuillez, Patrick |
author_facet | Chakir, Ibtissam Dumont, Stéphanie Pévet, Paul Ouarour, Ali Challet, Etienne Vuillez, Patrick |
author_sort | Chakir, Ibtissam |
collection | PubMed |
description | Nocturnal secretion of melatonin from the pineal gland may affect central and peripheral timing, in addition to its well-known involvement in the control of seasonal physiology. The Syrian hamster is a photoperiodic species, which displays gonadal atrophy and increased adiposity when adapted to short (winter-like) photoperiods. Here we investigated whether pineal melatonin secreted at night can impact daily rhythmicity of metabolic hormones and glucose in that seasonal species. For that purpose, daily variations of plasma leptin, cortisol, insulin and glucose were analyzed in pinealectomized hamsters, as compared to sham-operated controls kept under very long (16 h light/08 h dark) or short photoperiods (08 h light/16 h dark). Daily rhythms of leptin under both long and short photoperiods were blunted by pinealectomy. Furthermore, the phase of cortisol rhythm under a short photoperiod was advanced by 5.6 h after pinealectomy. Neither plasma insulin, nor blood glucose displays robust daily rhythmicity, even in sham-operated hamsters. Pinealectomy, however, totally reversed the decreased levels of insulin under short days and the photoperiodic variations in mean levels of blood glucose (i.e., reduction and increase in long and short days, respectively). Together, these findings in Syrian hamsters show that circulating melatonin at night drives the daily rhythmicity of plasma leptin, participates in the phase control of cortisol rhythm and modulates glucose homeostasis according to photoperiod-dependent metabolic state. |
format | Online Article Text |
id | pubmed-4444759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44447592015-06-12 Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters Chakir, Ibtissam Dumont, Stéphanie Pévet, Paul Ouarour, Ali Challet, Etienne Vuillez, Patrick Front Neurosci Endocrinology Nocturnal secretion of melatonin from the pineal gland may affect central and peripheral timing, in addition to its well-known involvement in the control of seasonal physiology. The Syrian hamster is a photoperiodic species, which displays gonadal atrophy and increased adiposity when adapted to short (winter-like) photoperiods. Here we investigated whether pineal melatonin secreted at night can impact daily rhythmicity of metabolic hormones and glucose in that seasonal species. For that purpose, daily variations of plasma leptin, cortisol, insulin and glucose were analyzed in pinealectomized hamsters, as compared to sham-operated controls kept under very long (16 h light/08 h dark) or short photoperiods (08 h light/16 h dark). Daily rhythms of leptin under both long and short photoperiods were blunted by pinealectomy. Furthermore, the phase of cortisol rhythm under a short photoperiod was advanced by 5.6 h after pinealectomy. Neither plasma insulin, nor blood glucose displays robust daily rhythmicity, even in sham-operated hamsters. Pinealectomy, however, totally reversed the decreased levels of insulin under short days and the photoperiodic variations in mean levels of blood glucose (i.e., reduction and increase in long and short days, respectively). Together, these findings in Syrian hamsters show that circulating melatonin at night drives the daily rhythmicity of plasma leptin, participates in the phase control of cortisol rhythm and modulates glucose homeostasis according to photoperiod-dependent metabolic state. Frontiers Media S.A. 2015-05-27 /pmc/articles/PMC4444759/ /pubmed/26074760 http://dx.doi.org/10.3389/fnins.2015.00190 Text en Copyright © 2015 Chakir, Dumont, Pévet, Ouarour, Challet and Vuillez. 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 | Endocrinology Chakir, Ibtissam Dumont, Stéphanie Pévet, Paul Ouarour, Ali Challet, Etienne Vuillez, Patrick Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title | Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title_full | Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title_fullStr | Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title_full_unstemmed | Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title_short | Pineal melatonin is a circadian time-giver for leptin rhythm in Syrian hamsters |
title_sort | pineal melatonin is a circadian time-giver for leptin rhythm in syrian hamsters |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444759/ https://www.ncbi.nlm.nih.gov/pubmed/26074760 http://dx.doi.org/10.3389/fnins.2015.00190 |
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