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Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats

STUDY OBJECTIVES: Millions suffer from sleep disorders that often accompany severe illnesses such as major depression; a leading psychiatric disorder characterized by appetite and rapid eye movement sleep (REMS) abnormalities. Melanin-concentrating hormone (MCH) and nesfatin-1/NUCB2 (nesfatin) are s...

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Autores principales: Vas, Szilvia, Ádori, Csaba, Könczöl, Katalin, Kátai, Zita, Pap, Dorottya, Papp, Rege S., Bagdy, György, Palkovits, Miklós, Tóth, Zsuzsanna E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613383/
https://www.ncbi.nlm.nih.gov/pubmed/23560056
http://dx.doi.org/10.1371/journal.pone.0059809
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author Vas, Szilvia
Ádori, Csaba
Könczöl, Katalin
Kátai, Zita
Pap, Dorottya
Papp, Rege S.
Bagdy, György
Palkovits, Miklós
Tóth, Zsuzsanna E.
author_facet Vas, Szilvia
Ádori, Csaba
Könczöl, Katalin
Kátai, Zita
Pap, Dorottya
Papp, Rege S.
Bagdy, György
Palkovits, Miklós
Tóth, Zsuzsanna E.
author_sort Vas, Szilvia
collection PubMed
description STUDY OBJECTIVES: Millions suffer from sleep disorders that often accompany severe illnesses such as major depression; a leading psychiatric disorder characterized by appetite and rapid eye movement sleep (REMS) abnormalities. Melanin-concentrating hormone (MCH) and nesfatin-1/NUCB2 (nesfatin) are strongly co - expressed in the hypothalamus and are involved both in food intake regulation and depression. Since MCH was recognized earlier as a hypnogenic factor, we analyzed the potential role of nesfatin on vigilance. DESIGN: We subjected rats to a 72 h-long REMS deprivation using the classic flower pot method, followed by a 3 h-long ‘rebound sleep’. Nesfatin mRNA and protein expressions as well as neuronal activity (Fos) were measured by quantitative in situ hybridization technique, ELISA and immunohistochemistry, respectively, in ‘deprived’ and ‘rebound’ groups, relative to controls sacrificed at the same time. We also analyzed electroencephalogram of rats treated by intracerebroventricularly administered nesfatin-1, or saline. RESULTS: REMS deprivation downregulated the expression of nesfatin (mRNA and protein), however, enhanced REMS during ‘rebound’ reversed this to control levels. Additionally, increased transcriptional activity (Fos) was demonstrated in nesfatin neurons during ‘rebound’. Centrally administered nesfatin-1 at light on reduced REMS and intermediate stage of sleep, while increased passive wake for several hours and also caused a short-term increase in light slow wave sleep. CONCLUSIONS: The data designate nesfatin as a potential new factor in sleep regulation, which fact can also be relevant in the better understanding of the role of nesfatin in the pathomechanism of depression.
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spelling pubmed-36133832013-04-04 Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats Vas, Szilvia Ádori, Csaba Könczöl, Katalin Kátai, Zita Pap, Dorottya Papp, Rege S. Bagdy, György Palkovits, Miklós Tóth, Zsuzsanna E. PLoS One Research Article STUDY OBJECTIVES: Millions suffer from sleep disorders that often accompany severe illnesses such as major depression; a leading psychiatric disorder characterized by appetite and rapid eye movement sleep (REMS) abnormalities. Melanin-concentrating hormone (MCH) and nesfatin-1/NUCB2 (nesfatin) are strongly co - expressed in the hypothalamus and are involved both in food intake regulation and depression. Since MCH was recognized earlier as a hypnogenic factor, we analyzed the potential role of nesfatin on vigilance. DESIGN: We subjected rats to a 72 h-long REMS deprivation using the classic flower pot method, followed by a 3 h-long ‘rebound sleep’. Nesfatin mRNA and protein expressions as well as neuronal activity (Fos) were measured by quantitative in situ hybridization technique, ELISA and immunohistochemistry, respectively, in ‘deprived’ and ‘rebound’ groups, relative to controls sacrificed at the same time. We also analyzed electroencephalogram of rats treated by intracerebroventricularly administered nesfatin-1, or saline. RESULTS: REMS deprivation downregulated the expression of nesfatin (mRNA and protein), however, enhanced REMS during ‘rebound’ reversed this to control levels. Additionally, increased transcriptional activity (Fos) was demonstrated in nesfatin neurons during ‘rebound’. Centrally administered nesfatin-1 at light on reduced REMS and intermediate stage of sleep, while increased passive wake for several hours and also caused a short-term increase in light slow wave sleep. CONCLUSIONS: The data designate nesfatin as a potential new factor in sleep regulation, which fact can also be relevant in the better understanding of the role of nesfatin in the pathomechanism of depression. Public Library of Science 2013-04-01 /pmc/articles/PMC3613383/ /pubmed/23560056 http://dx.doi.org/10.1371/journal.pone.0059809 Text en © 2013 Vas et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vas, Szilvia
Ádori, Csaba
Könczöl, Katalin
Kátai, Zita
Pap, Dorottya
Papp, Rege S.
Bagdy, György
Palkovits, Miklós
Tóth, Zsuzsanna E.
Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title_full Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title_fullStr Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title_full_unstemmed Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title_short Nesfatin-1/NUCB2 as a Potential New Element of Sleep Regulation in Rats
title_sort nesfatin-1/nucb2 as a potential new element of sleep regulation in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613383/
https://www.ncbi.nlm.nih.gov/pubmed/23560056
http://dx.doi.org/10.1371/journal.pone.0059809
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