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Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches

Songbirds provide a model for adult plasticity in the auditory cortex as a function of recent experience due to parallels with human auditory processing. As for speech processing in humans, activity in songbirds’ higher auditory cortex (caudomedial nidopallium, NCM) is lateralized for complex vocali...

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Autores principales: Furest Cataldo, Basilio, Yang, Lillian, Cabezas, Bryan, Ovetsky, Jonathan, Vicario, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681987/
https://www.ncbi.nlm.nih.gov/pubmed/38012325
http://dx.doi.org/10.1038/s42003-023-05567-7
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author Furest Cataldo, Basilio
Yang, Lillian
Cabezas, Bryan
Ovetsky, Jonathan
Vicario, David S.
author_facet Furest Cataldo, Basilio
Yang, Lillian
Cabezas, Bryan
Ovetsky, Jonathan
Vicario, David S.
author_sort Furest Cataldo, Basilio
collection PubMed
description Songbirds provide a model for adult plasticity in the auditory cortex as a function of recent experience due to parallels with human auditory processing. As for speech processing in humans, activity in songbirds’ higher auditory cortex (caudomedial nidopallium, NCM) is lateralized for complex vocalization sounds. However, in Zebra finches exposed to a novel heterospecific (canary) acoustic environment for 4–9 days, the typical pattern of right-lateralization is reversed. We now report that, in birds passively exposed to a novel heterospecific environment for extended periods (up to 21 days), the right-lateralized pattern of epidural auditory potentials first reverses transiently then returns to the typical pattern. Using acute, bilateral multi-unit electrophysiology, we confirm that this dynamic pattern occurs in NCM. Furthermore, extended exposure enhances discrimination for heterospecific stimuli. We conclude that lateralization is functionally labile and, when engaged by novel sensory experience, contributes to discrimination of novel stimuli that may be ethologically relevant. Future studies seek to determine whether, (1) the dynamicity of lateralized processes engaged by novel sensory experiences recurs with every novel challenge in the same organism; (2) the dynamic pattern extends to other cortical, thalamic or midbrain structures; and (3) the phenomenon generalizes across sensory modalities.
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spelling pubmed-106819872023-11-30 Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches Furest Cataldo, Basilio Yang, Lillian Cabezas, Bryan Ovetsky, Jonathan Vicario, David S. Commun Biol Article Songbirds provide a model for adult plasticity in the auditory cortex as a function of recent experience due to parallels with human auditory processing. As for speech processing in humans, activity in songbirds’ higher auditory cortex (caudomedial nidopallium, NCM) is lateralized for complex vocalization sounds. However, in Zebra finches exposed to a novel heterospecific (canary) acoustic environment for 4–9 days, the typical pattern of right-lateralization is reversed. We now report that, in birds passively exposed to a novel heterospecific environment for extended periods (up to 21 days), the right-lateralized pattern of epidural auditory potentials first reverses transiently then returns to the typical pattern. Using acute, bilateral multi-unit electrophysiology, we confirm that this dynamic pattern occurs in NCM. Furthermore, extended exposure enhances discrimination for heterospecific stimuli. We conclude that lateralization is functionally labile and, when engaged by novel sensory experience, contributes to discrimination of novel stimuli that may be ethologically relevant. Future studies seek to determine whether, (1) the dynamicity of lateralized processes engaged by novel sensory experiences recurs with every novel challenge in the same organism; (2) the dynamic pattern extends to other cortical, thalamic or midbrain structures; and (3) the phenomenon generalizes across sensory modalities. Nature Publishing Group UK 2023-11-27 /pmc/articles/PMC10681987/ /pubmed/38012325 http://dx.doi.org/10.1038/s42003-023-05567-7 Text en © The Author(s) 2023 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
Furest Cataldo, Basilio
Yang, Lillian
Cabezas, Bryan
Ovetsky, Jonathan
Vicario, David S.
Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title_full Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title_fullStr Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title_full_unstemmed Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title_short Novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
title_sort novel sound exposure drives dynamic changes in auditory lateralization that are associated with perceptual learning in zebra finches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681987/
https://www.ncbi.nlm.nih.gov/pubmed/38012325
http://dx.doi.org/10.1038/s42003-023-05567-7
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