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Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism
Excessive neural variability of sensory responses is a hallmark of atypical sensory processing in autistic individuals with cascading effects on other core autism symptoms but unknown neurobiological substrate. Here, by recording neocortical single neuron activity in a well-established mouse model o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689491/ https://www.ncbi.nlm.nih.gov/pubmed/38036566 http://dx.doi.org/10.1038/s41467-023-43777-z |
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author | Bhaskaran, Arjun A. Gauvrit, Théo Vyas, Yukti Bony, Guillaume Ginger, Melanie Frick, Andreas |
author_facet | Bhaskaran, Arjun A. Gauvrit, Théo Vyas, Yukti Bony, Guillaume Ginger, Melanie Frick, Andreas |
author_sort | Bhaskaran, Arjun A. |
collection | PubMed |
description | Excessive neural variability of sensory responses is a hallmark of atypical sensory processing in autistic individuals with cascading effects on other core autism symptoms but unknown neurobiological substrate. Here, by recording neocortical single neuron activity in a well-established mouse model of Fragile X syndrome and autism, we characterized atypical sensory processing and probed the role of endogenous noise sources in exaggerated response variability in males. The analysis of sensory stimulus evoked activity and spontaneous dynamics, as well as neuronal features, reveals a complex cellular and network phenotype. Neocortical sensory information processing is more variable and temporally imprecise. Increased trial-by-trial and inter-neuronal response variability is strongly related to key endogenous noise features, and may give rise to behavioural sensory responsiveness variability in autism. We provide a novel preclinical framework for understanding the sources of endogenous noise and its contribution to core autism symptoms, and for testing the functional consequences for mechanism-based manipulation of noise. |
format | Online Article Text |
id | pubmed-10689491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106894912023-12-02 Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism Bhaskaran, Arjun A. Gauvrit, Théo Vyas, Yukti Bony, Guillaume Ginger, Melanie Frick, Andreas Nat Commun Article Excessive neural variability of sensory responses is a hallmark of atypical sensory processing in autistic individuals with cascading effects on other core autism symptoms but unknown neurobiological substrate. Here, by recording neocortical single neuron activity in a well-established mouse model of Fragile X syndrome and autism, we characterized atypical sensory processing and probed the role of endogenous noise sources in exaggerated response variability in males. The analysis of sensory stimulus evoked activity and spontaneous dynamics, as well as neuronal features, reveals a complex cellular and network phenotype. Neocortical sensory information processing is more variable and temporally imprecise. Increased trial-by-trial and inter-neuronal response variability is strongly related to key endogenous noise features, and may give rise to behavioural sensory responsiveness variability in autism. We provide a novel preclinical framework for understanding the sources of endogenous noise and its contribution to core autism symptoms, and for testing the functional consequences for mechanism-based manipulation of noise. Nature Publishing Group UK 2023-11-30 /pmc/articles/PMC10689491/ /pubmed/38036566 http://dx.doi.org/10.1038/s41467-023-43777-z 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 Bhaskaran, Arjun A. Gauvrit, Théo Vyas, Yukti Bony, Guillaume Ginger, Melanie Frick, Andreas Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title | Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title_full | Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title_fullStr | Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title_full_unstemmed | Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title_short | Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1(−/y) mouse model of autism |
title_sort | endogenous noise of neocortical neurons correlates with atypical sensory response variability in the fmr1(−/y) mouse model of autism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689491/ https://www.ncbi.nlm.nih.gov/pubmed/38036566 http://dx.doi.org/10.1038/s41467-023-43777-z |
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