Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782455696101474304 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5037237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT timmenicholasm criticalitymaximizescomplexityinneuraltissue AT marshallnajjaj criticalitymaximizescomplexityinneuraltissue AT bennettnicholas criticalitymaximizescomplexityinneuraltissue AT rippmonica criticalitymaximizescomplexityinneuraltissue AT lautzenhiseredward criticalitymaximizescomplexityinneuraltissue AT beggsjohnm criticalitymaximizescomplexityinneuraltissue |