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Covert Waking Brain Activity Reveals Instantaneous Sleep Depth

The neural correlates of the wake-sleep continuum remain incompletely understood, limiting the development of adaptive drug delivery systems for promoting sleep maintenance. The most useful measure for resolving early positions along this continuum is the alpha oscillation, an 8–13 Hz electroencepha...

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Autores principales: McKinney, Scott M., Dang-Vu, Thien Thanh, Buxton, Orfeu M., Solet, Jo M., Ellenbogen, Jeffrey M.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048302/
https://www.ncbi.nlm.nih.gov/pubmed/21408616
http://dx.doi.org/10.1371/journal.pone.0017351
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author McKinney, Scott M.
Dang-Vu, Thien Thanh
Buxton, Orfeu M.
Solet, Jo M.
Ellenbogen, Jeffrey M.
author_facet McKinney, Scott M.
Dang-Vu, Thien Thanh
Buxton, Orfeu M.
Solet, Jo M.
Ellenbogen, Jeffrey M.
author_sort McKinney, Scott M.
collection PubMed
description The neural correlates of the wake-sleep continuum remain incompletely understood, limiting the development of adaptive drug delivery systems for promoting sleep maintenance. The most useful measure for resolving early positions along this continuum is the alpha oscillation, an 8–13 Hz electroencephalographic rhythm prominent over posterior scalp locations. The brain activation signature of wakefulness, alpha expression discloses immediate levels of alertness and dissipates in concert with fading awareness as sleep begins. This brain activity pattern, however, is largely ignored once sleep begins. Here we show that the intensity of spectral power in the alpha band actually continues to disclose instantaneous responsiveness to noise—a measure of sleep depth—throughout a night of sleep. By systematically challenging sleep with realistic and varied acoustic disruption, we found that sleepers exhibited markedly greater sensitivity to sounds during moments of elevated alpha expression. This result demonstrates that alpha power is not a binary marker of the transition between sleep and wakefulness, but carries rich information about immediate sleep stability. Further, it shows that an empirical and ecologically relevant form of sleep depth is revealed in real-time by EEG spectral content in the alpha band, a measure that affords prediction on the order of minutes. This signal, which transcends the boundaries of classical sleep stages, could potentially be used for real-time feedback to novel, adaptive drug delivery systems for inducing sleep.
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spelling pubmed-30483022011-03-15 Covert Waking Brain Activity Reveals Instantaneous Sleep Depth McKinney, Scott M. Dang-Vu, Thien Thanh Buxton, Orfeu M. Solet, Jo M. Ellenbogen, Jeffrey M. PLoS One Research Article The neural correlates of the wake-sleep continuum remain incompletely understood, limiting the development of adaptive drug delivery systems for promoting sleep maintenance. The most useful measure for resolving early positions along this continuum is the alpha oscillation, an 8–13 Hz electroencephalographic rhythm prominent over posterior scalp locations. The brain activation signature of wakefulness, alpha expression discloses immediate levels of alertness and dissipates in concert with fading awareness as sleep begins. This brain activity pattern, however, is largely ignored once sleep begins. Here we show that the intensity of spectral power in the alpha band actually continues to disclose instantaneous responsiveness to noise—a measure of sleep depth—throughout a night of sleep. By systematically challenging sleep with realistic and varied acoustic disruption, we found that sleepers exhibited markedly greater sensitivity to sounds during moments of elevated alpha expression. This result demonstrates that alpha power is not a binary marker of the transition between sleep and wakefulness, but carries rich information about immediate sleep stability. Further, it shows that an empirical and ecologically relevant form of sleep depth is revealed in real-time by EEG spectral content in the alpha band, a measure that affords prediction on the order of minutes. This signal, which transcends the boundaries of classical sleep stages, could potentially be used for real-time feedback to novel, adaptive drug delivery systems for inducing sleep. Public Library of Science 2011-03-03 /pmc/articles/PMC3048302/ /pubmed/21408616 http://dx.doi.org/10.1371/journal.pone.0017351 Text en McKinney 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
McKinney, Scott M.
Dang-Vu, Thien Thanh
Buxton, Orfeu M.
Solet, Jo M.
Ellenbogen, Jeffrey M.
Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title_full Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title_fullStr Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title_full_unstemmed Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title_short Covert Waking Brain Activity Reveals Instantaneous Sleep Depth
title_sort covert waking brain activity reveals instantaneous sleep depth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048302/
https://www.ncbi.nlm.nih.gov/pubmed/21408616
http://dx.doi.org/10.1371/journal.pone.0017351
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