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Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways

Sensory systems must continuously adapt to optimally encode stimuli encountered within the natural environment. The prevailing view is that such optimal coding comes at the cost of increased ambiguity, yet to date, prior studies have focused on artificial stimuli. Accordingly, here we investigated w...

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Autores principales: Carriot, Jerome, McAllister, Graham, Hooshangnejad, Hamed, Mackrous, Isabelle, Cullen, Kathleen E., Chacron, Maurice J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098492/
https://www.ncbi.nlm.nih.gov/pubmed/35551186
http://dx.doi.org/10.1038/s41467-022-30348-x
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author Carriot, Jerome
McAllister, Graham
Hooshangnejad, Hamed
Mackrous, Isabelle
Cullen, Kathleen E.
Chacron, Maurice J.
author_facet Carriot, Jerome
McAllister, Graham
Hooshangnejad, Hamed
Mackrous, Isabelle
Cullen, Kathleen E.
Chacron, Maurice J.
author_sort Carriot, Jerome
collection PubMed
description Sensory systems must continuously adapt to optimally encode stimuli encountered within the natural environment. The prevailing view is that such optimal coding comes at the cost of increased ambiguity, yet to date, prior studies have focused on artificial stimuli. Accordingly, here we investigated whether such a trade-off between optimality and ambiguity exists in the encoding of natural stimuli in the vestibular system. We recorded vestibular nuclei and their target vestibular thalamocortical neurons during naturalistic and artificial self-motion stimulation. Surprisingly, we found no trade-off between optimality and ambiguity. Using computational methods, we demonstrate that thalamocortical neural adaptation in the form of contrast gain control actually reduces coding ambiguity without compromising the optimality of coding under naturalistic but not artificial stimulation. Thus, taken together, our results challenge the common wisdom that adaptation leads to ambiguity and instead suggest an essential role in underlying unambiguous optimized encoding of natural stimuli.
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spelling pubmed-90984922022-05-14 Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways Carriot, Jerome McAllister, Graham Hooshangnejad, Hamed Mackrous, Isabelle Cullen, Kathleen E. Chacron, Maurice J. Nat Commun Article Sensory systems must continuously adapt to optimally encode stimuli encountered within the natural environment. The prevailing view is that such optimal coding comes at the cost of increased ambiguity, yet to date, prior studies have focused on artificial stimuli. Accordingly, here we investigated whether such a trade-off between optimality and ambiguity exists in the encoding of natural stimuli in the vestibular system. We recorded vestibular nuclei and their target vestibular thalamocortical neurons during naturalistic and artificial self-motion stimulation. Surprisingly, we found no trade-off between optimality and ambiguity. Using computational methods, we demonstrate that thalamocortical neural adaptation in the form of contrast gain control actually reduces coding ambiguity without compromising the optimality of coding under naturalistic but not artificial stimulation. Thus, taken together, our results challenge the common wisdom that adaptation leads to ambiguity and instead suggest an essential role in underlying unambiguous optimized encoding of natural stimuli. Nature Publishing Group UK 2022-05-12 /pmc/articles/PMC9098492/ /pubmed/35551186 http://dx.doi.org/10.1038/s41467-022-30348-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Carriot, Jerome
McAllister, Graham
Hooshangnejad, Hamed
Mackrous, Isabelle
Cullen, Kathleen E.
Chacron, Maurice J.
Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title_full Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title_fullStr Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title_full_unstemmed Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title_short Sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
title_sort sensory adaptation mediates efficient and unambiguous encoding of natural stimuli by vestibular thalamocortical pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098492/
https://www.ncbi.nlm.nih.gov/pubmed/35551186
http://dx.doi.org/10.1038/s41467-022-30348-x
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