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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6312400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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