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Network dynamics in nociceptive pathways assessed by the neuronal avalanche model
BACKGROUND: Traditional electroencephalography provides a critical assessment of pain responses. The perception of pain, however, may involve a series of signal transmission pathways in higher cortical function. Recent studies have shown that a mathematical method, the neuronal avalanche model, may...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478175/ https://www.ncbi.nlm.nih.gov/pubmed/22537828 http://dx.doi.org/10.1186/1744-8069-8-33 |
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author | Wu, José Jiun-Shian Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai-Chuang |
author_facet | Wu, José Jiun-Shian Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai-Chuang |
author_sort | Wu, José Jiun-Shian |
collection | PubMed |
description | BACKGROUND: Traditional electroencephalography provides a critical assessment of pain responses. The perception of pain, however, may involve a series of signal transmission pathways in higher cortical function. Recent studies have shown that a mathematical method, the neuronal avalanche model, may be applied to evaluate higher-order network dynamics. The neuronal avalanche is a cascade of neuronal activity, the size distribution of which can be approximated by a power law relationship manifested by the slope of a straight line (i.e., the α value). We investigated whether the neuronal avalanche could be a useful index for nociceptive assessment. FINDINGS: Neuronal activity was recorded with a 4 × 8 multichannel electrode array in the primary somatosensory cortex (S1) and anterior cingulate cortex (ACC). Under light anesthesia, peripheral pinch stimulation increased the slope of the α value in both the ACC and S1, whereas brush stimulation increased the α value only in the S1. The increase in α values was blocked in both regions under deep anesthesia. The increase in α values in the ACC induced by peripheral pinch stimulation was blocked by medial thalamic lesion, but the increase in α values in the S1 induced by brush and pinch stimulation was not affected. CONCLUSIONS: The neuronal avalanche model shows a critical state in the cortical network for noxious-related signal processing. The α value may provide an index of brain network activity that distinguishes the responses to somatic stimuli from the control state. These network dynamics may be valuable for the evaluation of acute nociceptive processes and may be applied to chronic pathological pain conditions. |
format | Online Article Text |
id | pubmed-3478175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34781752012-10-23 Network dynamics in nociceptive pathways assessed by the neuronal avalanche model Wu, José Jiun-Shian Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai-Chuang Mol Pain Short Report BACKGROUND: Traditional electroencephalography provides a critical assessment of pain responses. The perception of pain, however, may involve a series of signal transmission pathways in higher cortical function. Recent studies have shown that a mathematical method, the neuronal avalanche model, may be applied to evaluate higher-order network dynamics. The neuronal avalanche is a cascade of neuronal activity, the size distribution of which can be approximated by a power law relationship manifested by the slope of a straight line (i.e., the α value). We investigated whether the neuronal avalanche could be a useful index for nociceptive assessment. FINDINGS: Neuronal activity was recorded with a 4 × 8 multichannel electrode array in the primary somatosensory cortex (S1) and anterior cingulate cortex (ACC). Under light anesthesia, peripheral pinch stimulation increased the slope of the α value in both the ACC and S1, whereas brush stimulation increased the α value only in the S1. The increase in α values was blocked in both regions under deep anesthesia. The increase in α values in the ACC induced by peripheral pinch stimulation was blocked by medial thalamic lesion, but the increase in α values in the S1 induced by brush and pinch stimulation was not affected. CONCLUSIONS: The neuronal avalanche model shows a critical state in the cortical network for noxious-related signal processing. The α value may provide an index of brain network activity that distinguishes the responses to somatic stimuli from the control state. These network dynamics may be valuable for the evaluation of acute nociceptive processes and may be applied to chronic pathological pain conditions. BioMed Central 2012-04-26 /pmc/articles/PMC3478175/ /pubmed/22537828 http://dx.doi.org/10.1186/1744-8069-8-33 Text en Copyright ©2012 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. |
spellingShingle | Short Report Wu, José Jiun-Shian Shih, Hsi-Chien Yen, Chen-Tung Shyu, Bai-Chuang Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title | Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title_full | Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title_fullStr | Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title_full_unstemmed | Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title_short | Network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
title_sort | network dynamics in nociceptive pathways assessed by the neuronal avalanche model |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478175/ https://www.ncbi.nlm.nih.gov/pubmed/22537828 http://dx.doi.org/10.1186/1744-8069-8-33 |
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