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Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception

Recent research has identified late-latency, long-lasting neural activity as a robust correlate of conscious perception. Yet, the dynamical nature of this activity is poorly understood, and the mechanisms governing its presence or absence and the associated conscious perception remain elusive. We ap...

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Autores principales: Baria, Alexis T., Maniscalco, Brian, He, Biyu J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720802/
https://www.ncbi.nlm.nih.gov/pubmed/29176808
http://dx.doi.org/10.1371/journal.pcbi.1005806
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author Baria, Alexis T.
Maniscalco, Brian
He, Biyu J.
author_facet Baria, Alexis T.
Maniscalco, Brian
He, Biyu J.
author_sort Baria, Alexis T.
collection PubMed
description Recent research has identified late-latency, long-lasting neural activity as a robust correlate of conscious perception. Yet, the dynamical nature of this activity is poorly understood, and the mechanisms governing its presence or absence and the associated conscious perception remain elusive. We applied dynamic-pattern analysis to whole-brain slow (< 5 Hz) cortical dynamics recorded by magnetoencephalography (MEG) in human subjects performing a threshold-level visual perception task. Up to 1 second before stimulus onset, brain activity pattern across widespread cortices significantly predicted whether a threshold-level visual stimulus was later consciously perceived. This initial state of brain activity interacts nonlinearly with stimulus input to shape the evolving cortical activity trajectory, with seen and unseen trials following well separated trajectories. We observed that cortical activity trajectories during conscious perception are fast evolving and robust to small variations in the initial state. In addition, spontaneous brain activity pattern prior to stimulus onset also influences unconscious perceptual making in unseen trials. Together, these results suggest that brain dynamics underlying conscious visual perception belongs to the class of initial-state-dependent, robust, transient neural dynamics.
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spelling pubmed-57208022017-12-15 Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception Baria, Alexis T. Maniscalco, Brian He, Biyu J. PLoS Comput Biol Research Article Recent research has identified late-latency, long-lasting neural activity as a robust correlate of conscious perception. Yet, the dynamical nature of this activity is poorly understood, and the mechanisms governing its presence or absence and the associated conscious perception remain elusive. We applied dynamic-pattern analysis to whole-brain slow (< 5 Hz) cortical dynamics recorded by magnetoencephalography (MEG) in human subjects performing a threshold-level visual perception task. Up to 1 second before stimulus onset, brain activity pattern across widespread cortices significantly predicted whether a threshold-level visual stimulus was later consciously perceived. This initial state of brain activity interacts nonlinearly with stimulus input to shape the evolving cortical activity trajectory, with seen and unseen trials following well separated trajectories. We observed that cortical activity trajectories during conscious perception are fast evolving and robust to small variations in the initial state. In addition, spontaneous brain activity pattern prior to stimulus onset also influences unconscious perceptual making in unseen trials. Together, these results suggest that brain dynamics underlying conscious visual perception belongs to the class of initial-state-dependent, robust, transient neural dynamics. Public Library of Science 2017-11-27 /pmc/articles/PMC5720802/ /pubmed/29176808 http://dx.doi.org/10.1371/journal.pcbi.1005806 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Baria, Alexis T.
Maniscalco, Brian
He, Biyu J.
Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title_full Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title_fullStr Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title_full_unstemmed Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title_short Initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
title_sort initial-state-dependent, robust, transient neural dynamics encode conscious visual perception
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720802/
https://www.ncbi.nlm.nih.gov/pubmed/29176808
http://dx.doi.org/10.1371/journal.pcbi.1005806
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