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Auditory processing remains sensitive to environmental experience during adolescence in a rodent model

Elevated neural plasticity during development contributes to dramatic improvements in perceptual, motor, and cognitive skills. However, malleable neural circuits are vulnerable to environmental influences that may disrupt behavioral maturation. While these risks are well-established prior to sexual...

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Autores principales: Anbuhl, Kelsey L., Yao, Justin D., Hotz, Robert A., Mowery, Todd M., Sanes, Dan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130260/
https://www.ncbi.nlm.nih.gov/pubmed/35610222
http://dx.doi.org/10.1038/s41467-022-30455-9
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author Anbuhl, Kelsey L.
Yao, Justin D.
Hotz, Robert A.
Mowery, Todd M.
Sanes, Dan H.
author_facet Anbuhl, Kelsey L.
Yao, Justin D.
Hotz, Robert A.
Mowery, Todd M.
Sanes, Dan H.
author_sort Anbuhl, Kelsey L.
collection PubMed
description Elevated neural plasticity during development contributes to dramatic improvements in perceptual, motor, and cognitive skills. However, malleable neural circuits are vulnerable to environmental influences that may disrupt behavioral maturation. While these risks are well-established prior to sexual maturity (i.e., critical periods), the degree of neural vulnerability during adolescence remains uncertain. Here, we induce transient hearing loss (HL) spanning adolescence in gerbils, and ask whether behavioral and neural maturation are disrupted. We find that adolescent HL causes a significant perceptual deficit that can be attributed to degraded auditory cortex processing, as assessed with wireless single neuron recordings and within-session population-level analyses. Finally, auditory cortex brain slices from adolescent HL animals reveal synaptic deficits that are distinct from those typically observed after critical period deprivation. Taken together, these results show that diminished adolescent sensory experience can cause long-lasting behavioral deficits that originate, in part, from a dysfunctional cortical circuit.
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spelling pubmed-91302602022-05-26 Auditory processing remains sensitive to environmental experience during adolescence in a rodent model Anbuhl, Kelsey L. Yao, Justin D. Hotz, Robert A. Mowery, Todd M. Sanes, Dan H. Nat Commun Article Elevated neural plasticity during development contributes to dramatic improvements in perceptual, motor, and cognitive skills. However, malleable neural circuits are vulnerable to environmental influences that may disrupt behavioral maturation. While these risks are well-established prior to sexual maturity (i.e., critical periods), the degree of neural vulnerability during adolescence remains uncertain. Here, we induce transient hearing loss (HL) spanning adolescence in gerbils, and ask whether behavioral and neural maturation are disrupted. We find that adolescent HL causes a significant perceptual deficit that can be attributed to degraded auditory cortex processing, as assessed with wireless single neuron recordings and within-session population-level analyses. Finally, auditory cortex brain slices from adolescent HL animals reveal synaptic deficits that are distinct from those typically observed after critical period deprivation. Taken together, these results show that diminished adolescent sensory experience can cause long-lasting behavioral deficits that originate, in part, from a dysfunctional cortical circuit. Nature Publishing Group UK 2022-05-24 /pmc/articles/PMC9130260/ /pubmed/35610222 http://dx.doi.org/10.1038/s41467-022-30455-9 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
Anbuhl, Kelsey L.
Yao, Justin D.
Hotz, Robert A.
Mowery, Todd M.
Sanes, Dan H.
Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title_full Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title_fullStr Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title_full_unstemmed Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title_short Auditory processing remains sensitive to environmental experience during adolescence in a rodent model
title_sort auditory processing remains sensitive to environmental experience during adolescence in a rodent model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130260/
https://www.ncbi.nlm.nih.gov/pubmed/35610222
http://dx.doi.org/10.1038/s41467-022-30455-9
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