Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.

Slow oscillations are a hallmark of slow wave sleep. They provide a temporal framework for a variety of phasic events to occur and interact during sleep, including the expression of high-frequency oscillations and the discharge of neurons across the entire brain. Evidence shows that the emergence of...

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Main Authors: Miguel Valencia, Julio Artieda, J Paul Bolam, Juan Mena-Segovia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3699652?pdf=render
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spelling doaj-e3388cec57b344619b05c877f3f6750c2020-11-25T02:47:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e6754010.1371/journal.pone.0067540Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.Miguel ValenciaJulio ArtiedaJ Paul BolamJuan Mena-SegoviaSlow oscillations are a hallmark of slow wave sleep. They provide a temporal framework for a variety of phasic events to occur and interact during sleep, including the expression of high-frequency oscillations and the discharge of neurons across the entire brain. Evidence shows that the emergence of distinct high-frequency oscillations during slow oscillations facilitates the communication among brain regions whose activity was correlated during the preceding waking period. While the frequencies of oscillations involved in such interactions have been identified, their dynamics and the correlations between them require further investigation. Here we analyzed the structure and dynamics of these signals in anesthetized rats. We show that spindles and gamma oscillations coexist but have distinct temporal dynamics across the slow oscillation cycle. Furthermore, we observed that spindles and gamma are functionally coupled to the slow oscillations and between each other. Following the activation of ascending pathways from the brainstem by means of a carbachol injection in the pedunculopontine nucleus, we were able to modify the gain in the gamma oscillations that are independent of the spindles while the spindle amplitude was reduced. Furthermore, carbachol produced a decoupling of the gamma oscillations that are dependent on the spindles but with no effect on their amplitude. None of the changes in the high-frequency oscillations affected the onset or shape of the slow oscillations, suggesting that slow oscillations occur independently of the phasic events that coexist with them. Our results provide novel insights into the regulation, dynamics and homeostasis of cortical slow oscillations.http://europepmc.org/articles/PMC3699652?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Miguel Valencia
Julio Artieda
J Paul Bolam
Juan Mena-Segovia
spellingShingle Miguel Valencia
Julio Artieda
J Paul Bolam
Juan Mena-Segovia
Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
PLoS ONE
author_facet Miguel Valencia
Julio Artieda
J Paul Bolam
Juan Mena-Segovia
author_sort Miguel Valencia
title Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
title_short Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
title_full Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
title_fullStr Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
title_full_unstemmed Dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
title_sort dynamic interaction of spindles and gamma activity during cortical slow oscillations and its modulation by subcortical afferents.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Slow oscillations are a hallmark of slow wave sleep. They provide a temporal framework for a variety of phasic events to occur and interact during sleep, including the expression of high-frequency oscillations and the discharge of neurons across the entire brain. Evidence shows that the emergence of distinct high-frequency oscillations during slow oscillations facilitates the communication among brain regions whose activity was correlated during the preceding waking period. While the frequencies of oscillations involved in such interactions have been identified, their dynamics and the correlations between them require further investigation. Here we analyzed the structure and dynamics of these signals in anesthetized rats. We show that spindles and gamma oscillations coexist but have distinct temporal dynamics across the slow oscillation cycle. Furthermore, we observed that spindles and gamma are functionally coupled to the slow oscillations and between each other. Following the activation of ascending pathways from the brainstem by means of a carbachol injection in the pedunculopontine nucleus, we were able to modify the gain in the gamma oscillations that are independent of the spindles while the spindle amplitude was reduced. Furthermore, carbachol produced a decoupling of the gamma oscillations that are dependent on the spindles but with no effect on their amplitude. None of the changes in the high-frequency oscillations affected the onset or shape of the slow oscillations, suggesting that slow oscillations occur independently of the phasic events that coexist with them. Our results provide novel insights into the regulation, dynamics and homeostasis of cortical slow oscillations.
url http://europepmc.org/articles/PMC3699652?pdf=render
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