Probabilistic, entropy-maximizing control of large-scale neural synchronization.

Oscillatory neural activity is dynamically controlled to coordinate perceptual, attentional and cognitive processes. On the macroscopic scale, this control is reflected in the U-shaped deviations of EEG spectral-power dynamics from stochastic dynamics, characterized by disproportionately elevated oc...

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Main Authors: Melisa Menceloglu, Marcia Grabowecky, Satoru Suzuki
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0249317
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spelling doaj-7fc30516620f4e63867731871dd3c9582021-05-15T04:30:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01164e024931710.1371/journal.pone.0249317Probabilistic, entropy-maximizing control of large-scale neural synchronization.Melisa MencelogluMarcia GraboweckySatoru SuzukiOscillatory neural activity is dynamically controlled to coordinate perceptual, attentional and cognitive processes. On the macroscopic scale, this control is reflected in the U-shaped deviations of EEG spectral-power dynamics from stochastic dynamics, characterized by disproportionately elevated occurrences of the lowest and highest ranges of power. To understand the mechanisms that generate these low- and high-power states, we fit a simple mathematical model of synchronization of oscillatory activity to human EEG data. The results consistently indicated that the majority (~95%) of synchronization dynamics is controlled by slowly adjusting the probability of synchronization while maintaining maximum entropy within the timescale of a few seconds. This strategy appears to be universal as the results generalized across oscillation frequencies, EEG current sources, and participants (N = 52) whether they rested with their eyes closed, rested with their eyes open in a darkened room, or viewed a silent nature video. Given that precisely coordinated behavior requires tightly controlled oscillatory dynamics, the current results suggest that the large-scale spatial synchronization of oscillatory activity is controlled by the relatively slow, entropy-maximizing adjustments of synchronization probability (demonstrated here) in combination with temporally precise phase adjustments (e.g., phase resetting generated by sensorimotor interactions). Interestingly, we observed a modest but consistent spatial pattern of deviations from the maximum-entropy rule, potentially suggesting that the mid-central-posterior region serves as an "entropy dump" to facilitate the temporally precise control of spectral-power dynamics in the surrounding regions.https://doi.org/10.1371/journal.pone.0249317
collection DOAJ
language English
format Article
sources DOAJ
author Melisa Menceloglu
Marcia Grabowecky
Satoru Suzuki
spellingShingle Melisa Menceloglu
Marcia Grabowecky
Satoru Suzuki
Probabilistic, entropy-maximizing control of large-scale neural synchronization.
PLoS ONE
author_facet Melisa Menceloglu
Marcia Grabowecky
Satoru Suzuki
author_sort Melisa Menceloglu
title Probabilistic, entropy-maximizing control of large-scale neural synchronization.
title_short Probabilistic, entropy-maximizing control of large-scale neural synchronization.
title_full Probabilistic, entropy-maximizing control of large-scale neural synchronization.
title_fullStr Probabilistic, entropy-maximizing control of large-scale neural synchronization.
title_full_unstemmed Probabilistic, entropy-maximizing control of large-scale neural synchronization.
title_sort probabilistic, entropy-maximizing control of large-scale neural synchronization.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Oscillatory neural activity is dynamically controlled to coordinate perceptual, attentional and cognitive processes. On the macroscopic scale, this control is reflected in the U-shaped deviations of EEG spectral-power dynamics from stochastic dynamics, characterized by disproportionately elevated occurrences of the lowest and highest ranges of power. To understand the mechanisms that generate these low- and high-power states, we fit a simple mathematical model of synchronization of oscillatory activity to human EEG data. The results consistently indicated that the majority (~95%) of synchronization dynamics is controlled by slowly adjusting the probability of synchronization while maintaining maximum entropy within the timescale of a few seconds. This strategy appears to be universal as the results generalized across oscillation frequencies, EEG current sources, and participants (N = 52) whether they rested with their eyes closed, rested with their eyes open in a darkened room, or viewed a silent nature video. Given that precisely coordinated behavior requires tightly controlled oscillatory dynamics, the current results suggest that the large-scale spatial synchronization of oscillatory activity is controlled by the relatively slow, entropy-maximizing adjustments of synchronization probability (demonstrated here) in combination with temporally precise phase adjustments (e.g., phase resetting generated by sensorimotor interactions). Interestingly, we observed a modest but consistent spatial pattern of deviations from the maximum-entropy rule, potentially suggesting that the mid-central-posterior region serves as an "entropy dump" to facilitate the temporally precise control of spectral-power dynamics in the surrounding regions.
url https://doi.org/10.1371/journal.pone.0249317
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