A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.

We recently discovered, using Fos immunostaining, that the tuberal and mammillary hypothalamus contain a massive population of neurons specifically activated during paradoxical sleep (PS) hypersomnia. We further showed that some of the activated neurons of the tuberal hypothalamus express the melani...

Full description

Bibliographic Details
Main Authors: Emilie Sapin, Anne Bérod, Lucienne Léger, Paul A Herman, Pierre-Hervé Luppi, Christelle Peyron
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2909908?pdf=render
_version_ 1811265727106121728
author Emilie Sapin
Anne Bérod
Lucienne Léger
Paul A Herman
Pierre-Hervé Luppi
Christelle Peyron
author_facet Emilie Sapin
Anne Bérod
Lucienne Léger
Paul A Herman
Pierre-Hervé Luppi
Christelle Peyron
author_sort Emilie Sapin
collection DOAJ
description We recently discovered, using Fos immunostaining, that the tuberal and mammillary hypothalamus contain a massive population of neurons specifically activated during paradoxical sleep (PS) hypersomnia. We further showed that some of the activated neurons of the tuberal hypothalamus express the melanin concentrating hormone (MCH) neuropeptide and that icv injection of MCH induces a strong increase in PS quantity. However, the chemical nature of the majority of the neurons activated during PS had not been characterized. To determine whether these neurons are GABAergic, we combined in situ hybridization of GAD(67) mRNA with immunohistochemical detection of Fos in control, PS deprived and PS hypersomniac rats. We found that 74% of the very large population of Fos-labeled neurons located in the tuberal hypothalamus after PS hypersomnia were GAD-positive. We further demonstrated combining MCH immunohistochemistry and GAD(67)in situ hybridization that 85% of the MCH neurons were also GAD-positive. Finally, based on the number of Fos-ir/GAD(+), Fos-ir/MCH(+), and GAD(+)/MCH(+) double-labeled neurons counted from three sets of double-staining, we uncovered that around 80% of the large number of the Fos-ir/GAD(+) neurons located in the tuberal hypothalamus after PS hypersomnia do not contain MCH. Based on these and previous results, we propose that the non-MCH Fos/GABAergic neuronal population could be involved in PS induction and maintenance while the Fos/MCH/GABAergic neurons could be involved in the homeostatic regulation of PS. Further investigations will be needed to corroborate this original hypothesis.
first_indexed 2024-04-12T20:27:57Z
format Article
id doaj.art-24bddb0aceb94fef835fa06a75ffe05b
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-12T20:27:57Z
publishDate 2010-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-24bddb0aceb94fef835fa06a75ffe05b2022-12-22T03:17:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-0157e1176610.1371/journal.pone.0011766A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.Emilie SapinAnne BérodLucienne LégerPaul A HermanPierre-Hervé LuppiChristelle PeyronWe recently discovered, using Fos immunostaining, that the tuberal and mammillary hypothalamus contain a massive population of neurons specifically activated during paradoxical sleep (PS) hypersomnia. We further showed that some of the activated neurons of the tuberal hypothalamus express the melanin concentrating hormone (MCH) neuropeptide and that icv injection of MCH induces a strong increase in PS quantity. However, the chemical nature of the majority of the neurons activated during PS had not been characterized. To determine whether these neurons are GABAergic, we combined in situ hybridization of GAD(67) mRNA with immunohistochemical detection of Fos in control, PS deprived and PS hypersomniac rats. We found that 74% of the very large population of Fos-labeled neurons located in the tuberal hypothalamus after PS hypersomnia were GAD-positive. We further demonstrated combining MCH immunohistochemistry and GAD(67)in situ hybridization that 85% of the MCH neurons were also GAD-positive. Finally, based on the number of Fos-ir/GAD(+), Fos-ir/MCH(+), and GAD(+)/MCH(+) double-labeled neurons counted from three sets of double-staining, we uncovered that around 80% of the large number of the Fos-ir/GAD(+) neurons located in the tuberal hypothalamus after PS hypersomnia do not contain MCH. Based on these and previous results, we propose that the non-MCH Fos/GABAergic neuronal population could be involved in PS induction and maintenance while the Fos/MCH/GABAergic neurons could be involved in the homeostatic regulation of PS. Further investigations will be needed to corroborate this original hypothesis.http://europepmc.org/articles/PMC2909908?pdf=render
spellingShingle Emilie Sapin
Anne Bérod
Lucienne Léger
Paul A Herman
Pierre-Hervé Luppi
Christelle Peyron
A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
PLoS ONE
title A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
title_full A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
title_fullStr A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
title_full_unstemmed A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
title_short A very large number of GABAergic neurons are activated in the tuberal hypothalamus during paradoxical (REM) sleep hypersomnia.
title_sort very large number of gabaergic neurons are activated in the tuberal hypothalamus during paradoxical rem sleep hypersomnia
url http://europepmc.org/articles/PMC2909908?pdf=render
work_keys_str_mv AT emiliesapin averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT anneberod averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT lucienneleger averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT paulaherman averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT pierreherveluppi averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT christellepeyron averylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT emiliesapin verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT anneberod verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT lucienneleger verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT paulaherman verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT pierreherveluppi verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia
AT christellepeyron verylargenumberofgabaergicneuronsareactivatedinthetuberalhypothalamusduringparadoxicalremsleephypersomnia