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Plasticity of brain wave network interactions and evolution across physiologic states

Neural plasticity transcends a range of spatio-temporal scales and serves as the basis of various brain activities and physiologic functions. At the microscopic level, it enables the emergence of brain waves with complex temporal dynamics. At the macroscopic level, presence and dominance of specific...

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Autores principales: Liu, Kang K. L., Bartsch, Ronny P., Lin, Aijing, Mantegna, Rosario N., Ivanov, Plamen Ch.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620446/
https://www.ncbi.nlm.nih.gov/pubmed/26578891
http://dx.doi.org/10.3389/fncir.2015.00062
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author Liu, Kang K. L.
Bartsch, Ronny P.
Lin, Aijing
Mantegna, Rosario N.
Ivanov, Plamen Ch.
author_facet Liu, Kang K. L.
Bartsch, Ronny P.
Lin, Aijing
Mantegna, Rosario N.
Ivanov, Plamen Ch.
author_sort Liu, Kang K. L.
collection PubMed
description Neural plasticity transcends a range of spatio-temporal scales and serves as the basis of various brain activities and physiologic functions. At the microscopic level, it enables the emergence of brain waves with complex temporal dynamics. At the macroscopic level, presence and dominance of specific brain waves is associated with important brain functions. The role of neural plasticity at different levels in generating distinct brain rhythms and how brain rhythms communicate with each other across brain areas to generate physiologic states and functions remains not understood. Here we perform an empirical exploration of neural plasticity at the level of brain wave network interactions representing dynamical communications within and between different brain areas in the frequency domain. We introduce the concept of time delay stability (TDS) to quantify coordinated bursts in the activity of brain waves, and we employ a system-wide Network Physiology integrative approach to probe the network of coordinated brain wave activations and its evolution across physiologic states. We find an association between network structure and physiologic states. We uncover a hierarchical reorganization in the brain wave networks in response to changes in physiologic state, indicating new aspects of neural plasticity at the integrated level. Globally, we find that the entire brain network undergoes a pronounced transition from low connectivity in Deep Sleep and REM to high connectivity in Light Sleep and Wake. In contrast, we find that locally, different brain areas exhibit different network dynamics of brain wave interactions to achieve differentiation in function during different sleep stages. Moreover, our analyses indicate that plasticity also emerges in frequency-specific networks, which represent interactions across brain locations mediated through a specific frequency band. Comparing frequency-specific networks within the same physiologic state we find very different degree of network connectivity and link strength, while at the same time each frequency-specific network is characterized by a different signature pattern of sleep-stage stratification, reflecting a remarkable flexibility in response to change in physiologic state. These new aspects of neural plasticity demonstrate that in addition to dominant brain waves, the network of brain wave interactions is a previously unrecognized hallmark of physiologic state and function.
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spelling pubmed-46204462015-11-17 Plasticity of brain wave network interactions and evolution across physiologic states Liu, Kang K. L. Bartsch, Ronny P. Lin, Aijing Mantegna, Rosario N. Ivanov, Plamen Ch. Front Neural Circuits Neuroscience Neural plasticity transcends a range of spatio-temporal scales and serves as the basis of various brain activities and physiologic functions. At the microscopic level, it enables the emergence of brain waves with complex temporal dynamics. At the macroscopic level, presence and dominance of specific brain waves is associated with important brain functions. The role of neural plasticity at different levels in generating distinct brain rhythms and how brain rhythms communicate with each other across brain areas to generate physiologic states and functions remains not understood. Here we perform an empirical exploration of neural plasticity at the level of brain wave network interactions representing dynamical communications within and between different brain areas in the frequency domain. We introduce the concept of time delay stability (TDS) to quantify coordinated bursts in the activity of brain waves, and we employ a system-wide Network Physiology integrative approach to probe the network of coordinated brain wave activations and its evolution across physiologic states. We find an association between network structure and physiologic states. We uncover a hierarchical reorganization in the brain wave networks in response to changes in physiologic state, indicating new aspects of neural plasticity at the integrated level. Globally, we find that the entire brain network undergoes a pronounced transition from low connectivity in Deep Sleep and REM to high connectivity in Light Sleep and Wake. In contrast, we find that locally, different brain areas exhibit different network dynamics of brain wave interactions to achieve differentiation in function during different sleep stages. Moreover, our analyses indicate that plasticity also emerges in frequency-specific networks, which represent interactions across brain locations mediated through a specific frequency band. Comparing frequency-specific networks within the same physiologic state we find very different degree of network connectivity and link strength, while at the same time each frequency-specific network is characterized by a different signature pattern of sleep-stage stratification, reflecting a remarkable flexibility in response to change in physiologic state. These new aspects of neural plasticity demonstrate that in addition to dominant brain waves, the network of brain wave interactions is a previously unrecognized hallmark of physiologic state and function. Frontiers Media S.A. 2015-10-26 /pmc/articles/PMC4620446/ /pubmed/26578891 http://dx.doi.org/10.3389/fncir.2015.00062 Text en Copyright © 2015 Liu, Bartsch, Lin, Mantegna and Ivanov. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Liu, Kang K. L.
Bartsch, Ronny P.
Lin, Aijing
Mantegna, Rosario N.
Ivanov, Plamen Ch.
Plasticity of brain wave network interactions and evolution across physiologic states
title Plasticity of brain wave network interactions and evolution across physiologic states
title_full Plasticity of brain wave network interactions and evolution across physiologic states
title_fullStr Plasticity of brain wave network interactions and evolution across physiologic states
title_full_unstemmed Plasticity of brain wave network interactions and evolution across physiologic states
title_short Plasticity of brain wave network interactions and evolution across physiologic states
title_sort plasticity of brain wave network interactions and evolution across physiologic states
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620446/
https://www.ncbi.nlm.nih.gov/pubmed/26578891
http://dx.doi.org/10.3389/fncir.2015.00062
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