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Criticality Maximizes Complexity in Neural Tissue

The analysis of neural systems leverages tools from many different fields. Drawing on techniques from the study of critical phenomena in statistical mechanics, several studies have reported signatures of criticality in neural systems, including power-law distributions, shape collapses, and optimized...

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Autores principales: Timme, Nicholas M., Marshall, Najja J., Bennett, Nicholas, Ripp, Monica, Lautzenhiser, Edward, Beggs, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037237/
https://www.ncbi.nlm.nih.gov/pubmed/27729870
http://dx.doi.org/10.3389/fphys.2016.00425
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author Timme, Nicholas M.
Marshall, Najja J.
Bennett, Nicholas
Ripp, Monica
Lautzenhiser, Edward
Beggs, John M.
author_facet Timme, Nicholas M.
Marshall, Najja J.
Bennett, Nicholas
Ripp, Monica
Lautzenhiser, Edward
Beggs, John M.
author_sort Timme, Nicholas M.
collection PubMed
description The analysis of neural systems leverages tools from many different fields. Drawing on techniques from the study of critical phenomena in statistical mechanics, several studies have reported signatures of criticality in neural systems, including power-law distributions, shape collapses, and optimized quantities under tuning. Independently, neural complexity—an information theoretic measure—has been introduced in an effort to quantify the strength of correlations across multiple scales in a neural system. This measure represents an important tool in complex systems research because it allows for the quantification of the complexity of a neural system. In this analysis, we studied the relationships between neural complexity and criticality in neural culture data. We analyzed neural avalanches in 435 recordings from dissociated hippocampal cultures produced from rats, as well as neural avalanches from a cortical branching model. We utilized recently developed maximum likelihood estimation power-law fitting methods that account for doubly truncated power-laws, an automated shape collapse algorithm, and neural complexity and branching ratio calculation methods that account for sub-sampling, all of which are implemented in the freely available Neural Complexity and Criticality MATLAB toolbox. We found evidence that neural systems operate at or near a critical point and that neural complexity is optimized in these neural systems at or near the critical point. Surprisingly, we found evidence that complexity in neural systems is dependent upon avalanche profiles and neuron firing rate, but not precise spiking relationships between neurons. In order to facilitate future research, we made all of the culture data utilized in this analysis freely available online.
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spelling pubmed-50372372016-10-11 Criticality Maximizes Complexity in Neural Tissue Timme, Nicholas M. Marshall, Najja J. Bennett, Nicholas Ripp, Monica Lautzenhiser, Edward Beggs, John M. Front Physiol Physiology The analysis of neural systems leverages tools from many different fields. Drawing on techniques from the study of critical phenomena in statistical mechanics, several studies have reported signatures of criticality in neural systems, including power-law distributions, shape collapses, and optimized quantities under tuning. Independently, neural complexity—an information theoretic measure—has been introduced in an effort to quantify the strength of correlations across multiple scales in a neural system. This measure represents an important tool in complex systems research because it allows for the quantification of the complexity of a neural system. In this analysis, we studied the relationships between neural complexity and criticality in neural culture data. We analyzed neural avalanches in 435 recordings from dissociated hippocampal cultures produced from rats, as well as neural avalanches from a cortical branching model. We utilized recently developed maximum likelihood estimation power-law fitting methods that account for doubly truncated power-laws, an automated shape collapse algorithm, and neural complexity and branching ratio calculation methods that account for sub-sampling, all of which are implemented in the freely available Neural Complexity and Criticality MATLAB toolbox. We found evidence that neural systems operate at or near a critical point and that neural complexity is optimized in these neural systems at or near the critical point. Surprisingly, we found evidence that complexity in neural systems is dependent upon avalanche profiles and neuron firing rate, but not precise spiking relationships between neurons. In order to facilitate future research, we made all of the culture data utilized in this analysis freely available online. Frontiers Media S.A. 2016-09-27 /pmc/articles/PMC5037237/ /pubmed/27729870 http://dx.doi.org/10.3389/fphys.2016.00425 Text en Copyright © 2016 Timme, Marshall, Bennett, Ripp, Lautzenhiser and Beggs. 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 Physiology
Timme, Nicholas M.
Marshall, Najja J.
Bennett, Nicholas
Ripp, Monica
Lautzenhiser, Edward
Beggs, John M.
Criticality Maximizes Complexity in Neural Tissue
title Criticality Maximizes Complexity in Neural Tissue
title_full Criticality Maximizes Complexity in Neural Tissue
title_fullStr Criticality Maximizes Complexity in Neural Tissue
title_full_unstemmed Criticality Maximizes Complexity in Neural Tissue
title_short Criticality Maximizes Complexity in Neural Tissue
title_sort criticality maximizes complexity in neural tissue
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037237/
https://www.ncbi.nlm.nih.gov/pubmed/27729870
http://dx.doi.org/10.3389/fphys.2016.00425
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