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Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland
The role of the pineal gland is to translate the rhythmic cycles of night and day encoded by the retina into hormonal signals that are transmitted to the rest of the neuronal system in the form of serotonin and melatonin synthesis and release. Here we describe that the production of both melatonin a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378626/ https://www.ncbi.nlm.nih.gov/pubmed/22723743 http://dx.doi.org/10.1371/journal.pbio.1001347 |
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author | González, Sergio Moreno-Delgado, David Moreno, Estefanía Pérez-Capote, Kamil Franco, Rafael Mallol, Josefa Cortés, Antoni Casadó, Vicent Lluís, Carme Ortiz, Jordi Ferré, Sergi Canela, Enric McCormick, Peter J. |
author_facet | González, Sergio Moreno-Delgado, David Moreno, Estefanía Pérez-Capote, Kamil Franco, Rafael Mallol, Josefa Cortés, Antoni Casadó, Vicent Lluís, Carme Ortiz, Jordi Ferré, Sergi Canela, Enric McCormick, Peter J. |
author_sort | González, Sergio |
collection | PubMed |
description | The role of the pineal gland is to translate the rhythmic cycles of night and day encoded by the retina into hormonal signals that are transmitted to the rest of the neuronal system in the form of serotonin and melatonin synthesis and release. Here we describe that the production of both melatonin and serotonin by the pineal gland is regulated by a circadian-related heteromerization of adrenergic and dopamine D(4) receptors. Through α(1) (B)-D(4) and β(1)-D(4) receptor heteromers dopamine inhibits adrenergic receptor signaling and blocks the synthesis of melatonin induced by adrenergic receptor ligands. This inhibition was not observed at hours of the day when D(4) was not expressed. These data provide a new perspective on dopamine function and constitute the first example of a circadian-controlled receptor heteromer. The unanticipated heteromerization between adrenergic and dopamine D(4) receptors provides a feedback mechanism for the neuronal hormone system in the form of dopamine to control circadian inputs. |
format | Online Article Text |
id | pubmed-3378626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33786262012-06-21 Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland González, Sergio Moreno-Delgado, David Moreno, Estefanía Pérez-Capote, Kamil Franco, Rafael Mallol, Josefa Cortés, Antoni Casadó, Vicent Lluís, Carme Ortiz, Jordi Ferré, Sergi Canela, Enric McCormick, Peter J. PLoS Biol Research Article The role of the pineal gland is to translate the rhythmic cycles of night and day encoded by the retina into hormonal signals that are transmitted to the rest of the neuronal system in the form of serotonin and melatonin synthesis and release. Here we describe that the production of both melatonin and serotonin by the pineal gland is regulated by a circadian-related heteromerization of adrenergic and dopamine D(4) receptors. Through α(1) (B)-D(4) and β(1)-D(4) receptor heteromers dopamine inhibits adrenergic receptor signaling and blocks the synthesis of melatonin induced by adrenergic receptor ligands. This inhibition was not observed at hours of the day when D(4) was not expressed. These data provide a new perspective on dopamine function and constitute the first example of a circadian-controlled receptor heteromer. The unanticipated heteromerization between adrenergic and dopamine D(4) receptors provides a feedback mechanism for the neuronal hormone system in the form of dopamine to control circadian inputs. Public Library of Science 2012-06-19 /pmc/articles/PMC3378626/ /pubmed/22723743 http://dx.doi.org/10.1371/journal.pbio.1001347 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article González, Sergio Moreno-Delgado, David Moreno, Estefanía Pérez-Capote, Kamil Franco, Rafael Mallol, Josefa Cortés, Antoni Casadó, Vicent Lluís, Carme Ortiz, Jordi Ferré, Sergi Canela, Enric McCormick, Peter J. Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title | Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title_full | Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title_fullStr | Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title_full_unstemmed | Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title_short | Circadian-Related Heteromerization of Adrenergic and Dopamine D(4) Receptors Modulates Melatonin Synthesis and Release in the Pineal Gland |
title_sort | circadian-related heteromerization of adrenergic and dopamine d(4) receptors modulates melatonin synthesis and release in the pineal gland |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378626/ https://www.ncbi.nlm.nih.gov/pubmed/22723743 http://dx.doi.org/10.1371/journal.pbio.1001347 |
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