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Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing

Neural activity recorded at multiple spatiotemporal scales is dominated by arrhythmic fluctuations without a characteristic temporal periodicity. Such activity often exhibits a 1/f-type power spectrum, in which power falls off with increasing frequency following a power-law function: [Formula: see t...

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Autores principales: Lin, Amy, Maniscalco, Brian, He, Biyu J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075946/
https://www.ncbi.nlm.nih.gov/pubmed/27822495
http://dx.doi.org/10.1523/ENEURO.0191-16.2016
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author Lin, Amy
Maniscalco, Brian
He, Biyu J.
author_facet Lin, Amy
Maniscalco, Brian
He, Biyu J.
author_sort Lin, Amy
collection PubMed
description Neural activity recorded at multiple spatiotemporal scales is dominated by arrhythmic fluctuations without a characteristic temporal periodicity. Such activity often exhibits a 1/f-type power spectrum, in which power falls off with increasing frequency following a power-law function: [Formula: see text] , which is indicative of scale-free dynamics. Two extensively studied forms of scale-free neural dynamics in the human brain are slow cortical potentials (SCPs)—the low-frequency (<5 Hz) component of brain field potentials—and the amplitude fluctuations of α oscillations, both of which have been shown to carry important functional roles. In addition, scale-free dynamics characterize normal human physiology such as heartbeat dynamics. However, the exact relationships among these scale-free neural and physiological dynamics remain unclear. We recorded simultaneous magnetoencephalography and electrocardiography in healthy subjects in the resting state and while performing a discrimination task on scale-free dynamical auditory stimuli that followed different scale-free statistics. We observed that long-range temporal correlation (captured by the power-law exponent β) in SCPs positively correlated with that of heartbeat dynamics across time within an individual and negatively correlated with that of α-amplitude fluctuations across individuals. In addition, across individuals, long-range temporal correlation of both SCP and α-oscillation amplitude predicted subjects’ discrimination performance in the auditory task, albeit through antagonistic relationships. These findings reveal interrelations among different scale-free neural and physiological dynamics and initial evidence for the involvement of scale-free neural dynamics in the processing of natural stimuli, which often exhibit scale-free dynamics.
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spelling pubmed-50759462016-11-07 Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing Lin, Amy Maniscalco, Brian He, Biyu J. eNeuro New Research Neural activity recorded at multiple spatiotemporal scales is dominated by arrhythmic fluctuations without a characteristic temporal periodicity. Such activity often exhibits a 1/f-type power spectrum, in which power falls off with increasing frequency following a power-law function: [Formula: see text] , which is indicative of scale-free dynamics. Two extensively studied forms of scale-free neural dynamics in the human brain are slow cortical potentials (SCPs)—the low-frequency (<5 Hz) component of brain field potentials—and the amplitude fluctuations of α oscillations, both of which have been shown to carry important functional roles. In addition, scale-free dynamics characterize normal human physiology such as heartbeat dynamics. However, the exact relationships among these scale-free neural and physiological dynamics remain unclear. We recorded simultaneous magnetoencephalography and electrocardiography in healthy subjects in the resting state and while performing a discrimination task on scale-free dynamical auditory stimuli that followed different scale-free statistics. We observed that long-range temporal correlation (captured by the power-law exponent β) in SCPs positively correlated with that of heartbeat dynamics across time within an individual and negatively correlated with that of α-amplitude fluctuations across individuals. In addition, across individuals, long-range temporal correlation of both SCP and α-oscillation amplitude predicted subjects’ discrimination performance in the auditory task, albeit through antagonistic relationships. These findings reveal interrelations among different scale-free neural and physiological dynamics and initial evidence for the involvement of scale-free neural dynamics in the processing of natural stimuli, which often exhibit scale-free dynamics. Society for Neuroscience 2016-10-24 /pmc/articles/PMC5075946/ /pubmed/27822495 http://dx.doi.org/10.1523/ENEURO.0191-16.2016 Text en Copyright © 2016 Lin et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Lin, Amy
Maniscalco, Brian
He, Biyu J.
Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title_full Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title_fullStr Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title_full_unstemmed Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title_short Scale-Free Neural and Physiological Dynamics in Naturalistic Stimuli Processing
title_sort scale-free neural and physiological dynamics in naturalistic stimuli processing
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075946/
https://www.ncbi.nlm.nih.gov/pubmed/27822495
http://dx.doi.org/10.1523/ENEURO.0191-16.2016
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