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Feedback optimizes neural coding and perception of natural stimuli
Growing evidence suggests that sensory neurons achieve optimal encoding by matching their tuning properties to the natural stimulus statistics. However, the underlying mechanisms remain unclear. Here we demonstrate that feedback pathways from higher brain areas mediate optimized encoding of naturali...
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/PMC6181564/ https://www.ncbi.nlm.nih.gov/pubmed/30289387 http://dx.doi.org/10.7554/eLife.38935 |
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author | Huang, Chengjie G Metzen, Michael G Chacron, Maurice J |
author_facet | Huang, Chengjie G Metzen, Michael G Chacron, Maurice J |
author_sort | Huang, Chengjie G |
collection | PubMed |
description | Growing evidence suggests that sensory neurons achieve optimal encoding by matching their tuning properties to the natural stimulus statistics. However, the underlying mechanisms remain unclear. Here we demonstrate that feedback pathways from higher brain areas mediate optimized encoding of naturalistic stimuli via temporal whitening in the weakly electric fish Apteronotus leptorhynchus. While one source of direct feedback uniformly enhances neural responses, a separate source of indirect feedback selectively attenuates responses to low frequencies, thus creating a high-pass neural tuning curve that opposes the decaying spectral power of natural stimuli. Additionally, we recorded from two populations of higher brain neurons responsible for the direct and indirect descending inputs. While one population displayed broadband tuning, the other displayed high-pass tuning and thus performed temporal whitening. Hence, our results demonstrate a novel function for descending input in optimizing neural responses to sensory input through temporal whitening that is likely to be conserved across systems and species. |
format | Online Article Text |
id | pubmed-6181564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61815642018-10-18 Feedback optimizes neural coding and perception of natural stimuli Huang, Chengjie G Metzen, Michael G Chacron, Maurice J eLife Neuroscience Growing evidence suggests that sensory neurons achieve optimal encoding by matching their tuning properties to the natural stimulus statistics. However, the underlying mechanisms remain unclear. Here we demonstrate that feedback pathways from higher brain areas mediate optimized encoding of naturalistic stimuli via temporal whitening in the weakly electric fish Apteronotus leptorhynchus. While one source of direct feedback uniformly enhances neural responses, a separate source of indirect feedback selectively attenuates responses to low frequencies, thus creating a high-pass neural tuning curve that opposes the decaying spectral power of natural stimuli. Additionally, we recorded from two populations of higher brain neurons responsible for the direct and indirect descending inputs. While one population displayed broadband tuning, the other displayed high-pass tuning and thus performed temporal whitening. Hence, our results demonstrate a novel function for descending input in optimizing neural responses to sensory input through temporal whitening that is likely to be conserved across systems and species. eLife Sciences Publications, Ltd 2018-10-05 /pmc/articles/PMC6181564/ /pubmed/30289387 http://dx.doi.org/10.7554/eLife.38935 Text en © 2018, Huang 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 Huang, Chengjie G Metzen, Michael G Chacron, Maurice J Feedback optimizes neural coding and perception of natural stimuli |
title | Feedback optimizes neural coding and perception of natural stimuli |
title_full | Feedback optimizes neural coding and perception of natural stimuli |
title_fullStr | Feedback optimizes neural coding and perception of natural stimuli |
title_full_unstemmed | Feedback optimizes neural coding and perception of natural stimuli |
title_short | Feedback optimizes neural coding and perception of natural stimuli |
title_sort | feedback optimizes neural coding and perception of natural stimuli |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181564/ https://www.ncbi.nlm.nih.gov/pubmed/30289387 http://dx.doi.org/10.7554/eLife.38935 |
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