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Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior
Synthetic drug-like molecules that directly modulate the activity of key clock proteins offer the potential to directly modulate the endogenous circadian rhythm and treat diseases associated with clock dysfunction. Here, we demonstrate that synthetic ligands targeting a key component of the mammalia...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495958/ https://www.ncbi.nlm.nih.gov/pubmed/25536025 http://dx.doi.org/10.1038/ncomms6759 |
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author | Banerjee, Subhashis Wang, Yongjun Solt, Laura A. Griffett, Kristine Kazantzis, Melissa Amador, Ariadna El-Gendy, Bahaa M. Huitron-Resendiz, Salvador Roberts, Amanda J. Shin, Youseung Kamenecka, Theodore M. Burris, Thomas P. |
author_facet | Banerjee, Subhashis Wang, Yongjun Solt, Laura A. Griffett, Kristine Kazantzis, Melissa Amador, Ariadna El-Gendy, Bahaa M. Huitron-Resendiz, Salvador Roberts, Amanda J. Shin, Youseung Kamenecka, Theodore M. Burris, Thomas P. |
author_sort | Banerjee, Subhashis |
collection | PubMed |
description | Synthetic drug-like molecules that directly modulate the activity of key clock proteins offer the potential to directly modulate the endogenous circadian rhythm and treat diseases associated with clock dysfunction. Here, we demonstrate that synthetic ligands targeting a key component of the mammalian clock, the nuclear receptors REV-ERBα and β, regulate sleep architecture and emotional behavior in mice. REV-ERB agonists induce wakefulness and reduce REM and slow-wave sleep. Interestingly, REV-ERB agonists also reduce anxiety-like behavior. These data are consistent with increased anxiety-like behavior of REV-ERBβ null mice, in which REV-ERB agonists have no effect Also consistent with these effects being mediated by REV-ERB, the effect of the agonist on sleep and anxiety was suppressed by lithium treatment. These results indicate that pharmacological targeting of REVERB may lead to the development of novel therapeutics to treat sleep disorders and anxiety. |
format | Online Article Text |
id | pubmed-4495958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-44959582015-07-08 Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior Banerjee, Subhashis Wang, Yongjun Solt, Laura A. Griffett, Kristine Kazantzis, Melissa Amador, Ariadna El-Gendy, Bahaa M. Huitron-Resendiz, Salvador Roberts, Amanda J. Shin, Youseung Kamenecka, Theodore M. Burris, Thomas P. Nat Commun Article Synthetic drug-like molecules that directly modulate the activity of key clock proteins offer the potential to directly modulate the endogenous circadian rhythm and treat diseases associated with clock dysfunction. Here, we demonstrate that synthetic ligands targeting a key component of the mammalian clock, the nuclear receptors REV-ERBα and β, regulate sleep architecture and emotional behavior in mice. REV-ERB agonists induce wakefulness and reduce REM and slow-wave sleep. Interestingly, REV-ERB agonists also reduce anxiety-like behavior. These data are consistent with increased anxiety-like behavior of REV-ERBβ null mice, in which REV-ERB agonists have no effect Also consistent with these effects being mediated by REV-ERB, the effect of the agonist on sleep and anxiety was suppressed by lithium treatment. These results indicate that pharmacological targeting of REVERB may lead to the development of novel therapeutics to treat sleep disorders and anxiety. 2014-12-23 /pmc/articles/PMC4495958/ /pubmed/25536025 http://dx.doi.org/10.1038/ncomms6759 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Banerjee, Subhashis Wang, Yongjun Solt, Laura A. Griffett, Kristine Kazantzis, Melissa Amador, Ariadna El-Gendy, Bahaa M. Huitron-Resendiz, Salvador Roberts, Amanda J. Shin, Youseung Kamenecka, Theodore M. Burris, Thomas P. Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title | Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title_full | Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title_fullStr | Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title_full_unstemmed | Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title_short | Pharmacological Targeting of the Mammalian Clock Regulates Sleep Architecture and Emotional Behavior |
title_sort | pharmacological targeting of the mammalian clock regulates sleep architecture and emotional behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4495958/ https://www.ncbi.nlm.nih.gov/pubmed/25536025 http://dx.doi.org/10.1038/ncomms6759 |
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