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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9098492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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