Cargando…
Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli
The investigation of distributed coding across multiple neurons in the cortex remains to this date a challenge. Our current understanding of collective encoding of information and the relevant timescales is still limited. Most results are restricted to disparate timescales, focused on either very fa...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035626/ https://www.ncbi.nlm.nih.gov/pubmed/21346812 http://dx.doi.org/10.1371/journal.pone.0016758 |
_version_ | 1782197798456786944 |
---|---|
author | Jurjuţ, Ovidiu F. Nikolić, Danko Singer, Wolf Yu, Shan Havenith, Martha N. Mureşan, Raul C. |
author_facet | Jurjuţ, Ovidiu F. Nikolić, Danko Singer, Wolf Yu, Shan Havenith, Martha N. Mureşan, Raul C. |
author_sort | Jurjuţ, Ovidiu F. |
collection | PubMed |
description | The investigation of distributed coding across multiple neurons in the cortex remains to this date a challenge. Our current understanding of collective encoding of information and the relevant timescales is still limited. Most results are restricted to disparate timescales, focused on either very fast, e.g., spike-synchrony, or slow timescales, e.g., firing rate. Here, we investigated systematically multineuronal activity patterns evolving on different timescales, spanning the whole range from spike-synchrony to mean firing rate. Using multi-electrode recordings from cat visual cortex, we show that cortical responses can be described as trajectories in a high-dimensional pattern space. Patterns evolve on a continuum of coexisting timescales that strongly relate to the temporal properties of stimuli. Timescales consistent with the time constants of neuronal membranes and fast synaptic transmission (5–20 ms) play a particularly salient role in encoding a large amount of stimulus-related information. Thus, to faithfully encode the properties of visual stimuli the brain engages multiple neurons into activity patterns evolving on multiple timescales. |
format | Text |
id | pubmed-3035626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30356262011-02-23 Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli Jurjuţ, Ovidiu F. Nikolić, Danko Singer, Wolf Yu, Shan Havenith, Martha N. Mureşan, Raul C. PLoS One Research Article The investigation of distributed coding across multiple neurons in the cortex remains to this date a challenge. Our current understanding of collective encoding of information and the relevant timescales is still limited. Most results are restricted to disparate timescales, focused on either very fast, e.g., spike-synchrony, or slow timescales, e.g., firing rate. Here, we investigated systematically multineuronal activity patterns evolving on different timescales, spanning the whole range from spike-synchrony to mean firing rate. Using multi-electrode recordings from cat visual cortex, we show that cortical responses can be described as trajectories in a high-dimensional pattern space. Patterns evolve on a continuum of coexisting timescales that strongly relate to the temporal properties of stimuli. Timescales consistent with the time constants of neuronal membranes and fast synaptic transmission (5–20 ms) play a particularly salient role in encoding a large amount of stimulus-related information. Thus, to faithfully encode the properties of visual stimuli the brain engages multiple neurons into activity patterns evolving on multiple timescales. Public Library of Science 2011-02-08 /pmc/articles/PMC3035626/ /pubmed/21346812 http://dx.doi.org/10.1371/journal.pone.0016758 Text en Jurjuţ et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Jurjuţ, Ovidiu F. Nikolić, Danko Singer, Wolf Yu, Shan Havenith, Martha N. Mureşan, Raul C. Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title | Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title_full | Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title_fullStr | Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title_full_unstemmed | Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title_short | Timescales of Multineuronal Activity Patterns Reflect Temporal Structure of Visual Stimuli |
title_sort | timescales of multineuronal activity patterns reflect temporal structure of visual stimuli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035626/ https://www.ncbi.nlm.nih.gov/pubmed/21346812 http://dx.doi.org/10.1371/journal.pone.0016758 |
work_keys_str_mv | AT jurjutovidiuf timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli AT nikolicdanko timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli AT singerwolf timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli AT yushan timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli AT havenithmarthan timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli AT muresanraulc timescalesofmultineuronalactivitypatternsreflecttemporalstructureofvisualstimuli |