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Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs
BACKGROUND: Cortical neurons display network-level dynamics with unique spatiotemporal patterns that construct the backbone of processing information signals and contribute to higher functions. Recent years have seen a wealth of research on the characteristics of neuronal networks that are sufficien...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893465/ https://www.ncbi.nlm.nih.gov/pubmed/24387299 http://dx.doi.org/10.1186/1471-2202-15-3 |
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author | Wu, José Jiun-Shian Chang, Wei-Pang Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai Chuang |
author_facet | Wu, José Jiun-Shian Chang, Wei-Pang Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai Chuang |
author_sort | Wu, José Jiun-Shian |
collection | PubMed |
description | BACKGROUND: Cortical neurons display network-level dynamics with unique spatiotemporal patterns that construct the backbone of processing information signals and contribute to higher functions. Recent years have seen a wealth of research on the characteristics of neuronal networks that are sufficient conditions to activate or cease network functions. Local field potentials (LFPs) exhibit a scale-free and unique event size distribution (i.e., a neuronal avalanche) that has been proven in the cortex across species, including mice, rats, and humans, and may be used as an index of cortical excitability. In the present study, we induced seizure activity in the anterior cingulate cortex (ACC) with medial thalamic inputs and evaluated the impact of cortical excitability and thalamic inputs on network-level dynamics. We measured LFPs from multi-electrode recordings in mouse cortical slices and isoflurane-anesthetized rats. RESULTS: The ACC activity exhibited a neuronal avalanche with regard to avalanche size distribution, and the slope of the power-law distribution of the neuronal avalanche reflected network excitability in vitro and in vivo. We found that the slope of the neuronal avalanche in seizure-like activity significantly correlated with cortical excitability induced by γ-aminobutyric acid system manipulation. The thalamic inputs desynchronized cingulate seizures and affected the level of cortical excitability, the modulation of which could be determined by the slope of the avalanche size. CONCLUSIONS: We propose that the neuronal avalanche may be a tool for analyzing cortical activity through LFPs to determine alterations in network dynamics. |
format | Online Article Text |
id | pubmed-3893465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38934652014-01-27 Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs Wu, José Jiun-Shian Chang, Wei-Pang Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai Chuang BMC Neurosci Research Article BACKGROUND: Cortical neurons display network-level dynamics with unique spatiotemporal patterns that construct the backbone of processing information signals and contribute to higher functions. Recent years have seen a wealth of research on the characteristics of neuronal networks that are sufficient conditions to activate or cease network functions. Local field potentials (LFPs) exhibit a scale-free and unique event size distribution (i.e., a neuronal avalanche) that has been proven in the cortex across species, including mice, rats, and humans, and may be used as an index of cortical excitability. In the present study, we induced seizure activity in the anterior cingulate cortex (ACC) with medial thalamic inputs and evaluated the impact of cortical excitability and thalamic inputs on network-level dynamics. We measured LFPs from multi-electrode recordings in mouse cortical slices and isoflurane-anesthetized rats. RESULTS: The ACC activity exhibited a neuronal avalanche with regard to avalanche size distribution, and the slope of the power-law distribution of the neuronal avalanche reflected network excitability in vitro and in vivo. We found that the slope of the neuronal avalanche in seizure-like activity significantly correlated with cortical excitability induced by γ-aminobutyric acid system manipulation. The thalamic inputs desynchronized cingulate seizures and affected the level of cortical excitability, the modulation of which could be determined by the slope of the avalanche size. CONCLUSIONS: We propose that the neuronal avalanche may be a tool for analyzing cortical activity through LFPs to determine alterations in network dynamics. BioMed Central 2014-01-03 /pmc/articles/PMC3893465/ /pubmed/24387299 http://dx.doi.org/10.1186/1471-2202-15-3 Text en Copyright © 2014 Wu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wu, José Jiun-Shian Chang, Wei-Pang Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai Chuang Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title | Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title_full | Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title_fullStr | Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title_full_unstemmed | Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title_short | Cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
title_sort | cingulate seizure-like activity reveals neuronal avalanche regulated by network excitability and thalamic inputs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893465/ https://www.ncbi.nlm.nih.gov/pubmed/24387299 http://dx.doi.org/10.1186/1471-2202-15-3 |
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