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Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways

It is commonly assumed that the brain’s neural coding strategies are adapted to the statistics of natural stimuli. Specifically, to maximize information transmission, a sensory neuron’s tuning function should effectively oppose the decaying stimulus spectral power, such that the neural response is t...

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Autores principales: Mitchell, Diana E, Kwan, Annie, Carriot, Jerome, Chacron, Maurice J, Cullen, Kathleen E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312400/
https://www.ncbi.nlm.nih.gov/pubmed/30561328
http://dx.doi.org/10.7554/eLife.43019
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author Mitchell, Diana E
Kwan, Annie
Carriot, Jerome
Chacron, Maurice J
Cullen, Kathleen E
author_facet Mitchell, Diana E
Kwan, Annie
Carriot, Jerome
Chacron, Maurice J
Cullen, Kathleen E
author_sort Mitchell, Diana E
collection PubMed
description It is commonly assumed that the brain’s neural coding strategies are adapted to the statistics of natural stimuli. Specifically, to maximize information transmission, a sensory neuron’s tuning function should effectively oppose the decaying stimulus spectral power, such that the neural response is temporally decorrelated (i.e. ‘whitened’). However, theory predicts that the structure of neuronal variability also plays an essential role in determining how coding is optimized. Here, we provide experimental evidence supporting this view by recording from neurons in early vestibular pathways during naturalistic self-motion. We found that central vestibular neurons displayed temporally whitened responses that could not be explained by their tuning alone. Rather, computational modeling and analysis revealed that neuronal variability and tuning were matched to effectively complement natural stimulus statistics, thereby achieving temporal decorrelation and optimizing information transmission. Taken together, our findings reveal a novel strategy by which neural variability contributes to optimized processing of naturalistic stimuli.
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spelling pubmed-63124002019-01-04 Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways Mitchell, Diana E Kwan, Annie Carriot, Jerome Chacron, Maurice J Cullen, Kathleen E eLife Neuroscience It is commonly assumed that the brain’s neural coding strategies are adapted to the statistics of natural stimuli. Specifically, to maximize information transmission, a sensory neuron’s tuning function should effectively oppose the decaying stimulus spectral power, such that the neural response is temporally decorrelated (i.e. ‘whitened’). However, theory predicts that the structure of neuronal variability also plays an essential role in determining how coding is optimized. Here, we provide experimental evidence supporting this view by recording from neurons in early vestibular pathways during naturalistic self-motion. We found that central vestibular neurons displayed temporally whitened responses that could not be explained by their tuning alone. Rather, computational modeling and analysis revealed that neuronal variability and tuning were matched to effectively complement natural stimulus statistics, thereby achieving temporal decorrelation and optimizing information transmission. Taken together, our findings reveal a novel strategy by which neural variability contributes to optimized processing of naturalistic stimuli. eLife Sciences Publications, Ltd 2018-12-18 /pmc/articles/PMC6312400/ /pubmed/30561328 http://dx.doi.org/10.7554/eLife.43019 Text en © 2018, Mitchell et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mitchell, Diana E
Kwan, Annie
Carriot, Jerome
Chacron, Maurice J
Cullen, Kathleen E
Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title_full Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title_fullStr Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title_full_unstemmed Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title_short Neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
title_sort neuronal variability and tuning are balanced to optimize naturalistic self-motion coding in primate vestibular pathways
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312400/
https://www.ncbi.nlm.nih.gov/pubmed/30561328
http://dx.doi.org/10.7554/eLife.43019
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