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Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex
Neurons in the primary somatosensory cortex (S1) respond to peripheral stimulation with synchronized bursts of spikes, which lock to the macroscopic 600-Hz EEG waves. The mechanism of burst generation and synchronization in S1 is not yet understood. Using models of single-neuron responses fitted to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566798/ https://www.ncbi.nlm.nih.gov/pubmed/28840189 http://dx.doi.org/10.1523/ENEURO.0173-17.2017 |
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author | Teleńczuk, Bartosz Kempter, Richard Curio, Gabriel Destexhe, Alain |
author_facet | Teleńczuk, Bartosz Kempter, Richard Curio, Gabriel Destexhe, Alain |
author_sort | Teleńczuk, Bartosz |
collection | PubMed |
description | Neurons in the primary somatosensory cortex (S1) respond to peripheral stimulation with synchronized bursts of spikes, which lock to the macroscopic 600-Hz EEG waves. The mechanism of burst generation and synchronization in S1 is not yet understood. Using models of single-neuron responses fitted to unit recordings from macaque monkeys, we show that these synchronized bursts are the consequence of correlated synaptic inputs combined with a refractory mechanism. In the presence of noise these models reproduce also the observed trial-to-trial response variability, where individual bursts represent one of many stereotypical temporal spike patterns. When additional slower and global excitability fluctuations are introduced the single-neuron spike patterns are correlated with the population activity, as demonstrated in experimental data. The underlying biophysical mechanism of S1 responses involves thalamic inputs arriving through depressing synapses to cortical neurons in a high-conductance state. Our findings show that a simple feedforward processing of peripheral inputs could give rise to neuronal responses with nontrivial temporal and population statistics. We conclude that neural systems could use refractoriness to encode variable cortical states into stereotypical short-term spike patterns amenable to processing at neuronal time scales (tens of milliseconds). |
format | Online Article Text |
id | pubmed-5566798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-55667982017-08-24 Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex Teleńczuk, Bartosz Kempter, Richard Curio, Gabriel Destexhe, Alain eNeuro New Research Neurons in the primary somatosensory cortex (S1) respond to peripheral stimulation with synchronized bursts of spikes, which lock to the macroscopic 600-Hz EEG waves. The mechanism of burst generation and synchronization in S1 is not yet understood. Using models of single-neuron responses fitted to unit recordings from macaque monkeys, we show that these synchronized bursts are the consequence of correlated synaptic inputs combined with a refractory mechanism. In the presence of noise these models reproduce also the observed trial-to-trial response variability, where individual bursts represent one of many stereotypical temporal spike patterns. When additional slower and global excitability fluctuations are introduced the single-neuron spike patterns are correlated with the population activity, as demonstrated in experimental data. The underlying biophysical mechanism of S1 responses involves thalamic inputs arriving through depressing synapses to cortical neurons in a high-conductance state. Our findings show that a simple feedforward processing of peripheral inputs could give rise to neuronal responses with nontrivial temporal and population statistics. We conclude that neural systems could use refractoriness to encode variable cortical states into stereotypical short-term spike patterns amenable to processing at neuronal time scales (tens of milliseconds). Society for Neuroscience 2017-08-23 /pmc/articles/PMC5566798/ /pubmed/28840189 http://dx.doi.org/10.1523/ENEURO.0173-17.2017 Text en Copyright © 2017 Teleńczuk et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | New Research Teleńczuk, Bartosz Kempter, Richard Curio, Gabriel Destexhe, Alain Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title | Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title_full | Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title_fullStr | Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title_full_unstemmed | Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title_short | Refractoriness Accounts for Variable Spike Burst Responses in Somatosensory Cortex |
title_sort | refractoriness accounts for variable spike burst responses in somatosensory cortex |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566798/ https://www.ncbi.nlm.nih.gov/pubmed/28840189 http://dx.doi.org/10.1523/ENEURO.0173-17.2017 |
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