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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...

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Autores principales: Teleńczuk, Bartosz, Kempter, Richard, Curio, Gabriel, Destexhe, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2017
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).
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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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