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Partitioning neuronal variability

Responses of sensory neurons differ across repeated measurements. This variability is usually treated as stochasticity arising within neurons or neural circuits. However, some portion of the variability arises from fluctuations in excitability due to factors that are not purely sensory, such as arou...

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Detalles Bibliográficos
Autores principales: Goris, Robbe L.T., Movshon, J. Anthony, Simoncelli, Eero P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135707/
https://www.ncbi.nlm.nih.gov/pubmed/24777419
http://dx.doi.org/10.1038/nn.3711
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author Goris, Robbe L.T.
Movshon, J. Anthony
Simoncelli, Eero P.
author_facet Goris, Robbe L.T.
Movshon, J. Anthony
Simoncelli, Eero P.
author_sort Goris, Robbe L.T.
collection PubMed
description Responses of sensory neurons differ across repeated measurements. This variability is usually treated as stochasticity arising within neurons or neural circuits. However, some portion of the variability arises from fluctuations in excitability due to factors that are not purely sensory, such as arousal, attention, and adaptation. To isolate these fluctuations, we developed a model in which spikes are generated by a Poisson process whose rate is the product of a drive that is sensory in origin, and a gain summarizing stimulus-independent modulatory influences on excitability. This model provides an accurate account of response distributions of visual neurons in macaque LGN, V1, V2, and MT, revealing that variability originates in large part from excitability fluctuations which are correlated over time and between neurons, and which increase in strength along the visual pathway. The model provides a parsimonious explanation for observed systematic dependencies of response variability and covariability on firing rate.
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spelling pubmed-41357072014-12-01 Partitioning neuronal variability Goris, Robbe L.T. Movshon, J. Anthony Simoncelli, Eero P. Nat Neurosci Article Responses of sensory neurons differ across repeated measurements. This variability is usually treated as stochasticity arising within neurons or neural circuits. However, some portion of the variability arises from fluctuations in excitability due to factors that are not purely sensory, such as arousal, attention, and adaptation. To isolate these fluctuations, we developed a model in which spikes are generated by a Poisson process whose rate is the product of a drive that is sensory in origin, and a gain summarizing stimulus-independent modulatory influences on excitability. This model provides an accurate account of response distributions of visual neurons in macaque LGN, V1, V2, and MT, revealing that variability originates in large part from excitability fluctuations which are correlated over time and between neurons, and which increase in strength along the visual pathway. The model provides a parsimonious explanation for observed systematic dependencies of response variability and covariability on firing rate. 2014-04-28 2014-06 /pmc/articles/PMC4135707/ /pubmed/24777419 http://dx.doi.org/10.1038/nn.3711 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Goris, Robbe L.T.
Movshon, J. Anthony
Simoncelli, Eero P.
Partitioning neuronal variability
title Partitioning neuronal variability
title_full Partitioning neuronal variability
title_fullStr Partitioning neuronal variability
title_full_unstemmed Partitioning neuronal variability
title_short Partitioning neuronal variability
title_sort partitioning neuronal variability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135707/
https://www.ncbi.nlm.nih.gov/pubmed/24777419
http://dx.doi.org/10.1038/nn.3711
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