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Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones
Repetition plasticity is a ubiquitous property of sensory systems in which repetitive sensation causes either a decrease (“repetition suppression”, i.e. “adaptation”) or increase (“repetition enhancement”, i.e. “facilitation”) in the amplitude of neural responses. Timescales of repetition plasticity...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168329/ https://www.ncbi.nlm.nih.gov/pubmed/37162964 http://dx.doi.org/10.1101/2023.04.26.538446 |
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author | Gill, Nasiru K. Francis, Nikolas A. |
author_facet | Gill, Nasiru K. Francis, Nikolas A. |
author_sort | Gill, Nasiru K. |
collection | PubMed |
description | Repetition plasticity is a ubiquitous property of sensory systems in which repetitive sensation causes either a decrease (“repetition suppression”, i.e. “adaptation”) or increase (“repetition enhancement”, i.e. “facilitation”) in the amplitude of neural responses. Timescales of repetition plasticity for sensory neurons typically span milliseconds to tens of seconds, with longer durations for cortical vs subcortical regions. Here, we used 2-photon (2P) imaging to study repetition plasticity in mouse primary auditory cortex (A1) layer 2/3 (L2/3) during the presentation of spectrotemporally randomized pure-tone frequencies. Our study revealed subpopulations of neurons with repetition plasticity for equiprobable frequencies spaced minutes apart over a 20-minute period. We found both repetition suppression and enhancement in individual neurons and on average across populations. Each neuron tended to show repetition plasticity for 1–2 pure-tone frequencies near the neuron’s best frequency. Moreover, we found correlated changes in neural response amplitude and latency across stimulus repetitions. Together, our results highlight cortical specialization for pattern recognition over long timescales in complex acoustic sequences. |
format | Online Article Text |
id | pubmed-10168329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101683292023-05-10 Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones Gill, Nasiru K. Francis, Nikolas A. bioRxiv Article Repetition plasticity is a ubiquitous property of sensory systems in which repetitive sensation causes either a decrease (“repetition suppression”, i.e. “adaptation”) or increase (“repetition enhancement”, i.e. “facilitation”) in the amplitude of neural responses. Timescales of repetition plasticity for sensory neurons typically span milliseconds to tens of seconds, with longer durations for cortical vs subcortical regions. Here, we used 2-photon (2P) imaging to study repetition plasticity in mouse primary auditory cortex (A1) layer 2/3 (L2/3) during the presentation of spectrotemporally randomized pure-tone frequencies. Our study revealed subpopulations of neurons with repetition plasticity for equiprobable frequencies spaced minutes apart over a 20-minute period. We found both repetition suppression and enhancement in individual neurons and on average across populations. Each neuron tended to show repetition plasticity for 1–2 pure-tone frequencies near the neuron’s best frequency. Moreover, we found correlated changes in neural response amplitude and latency across stimulus repetitions. Together, our results highlight cortical specialization for pattern recognition over long timescales in complex acoustic sequences. Cold Spring Harbor Laboratory 2023-04-28 /pmc/articles/PMC10168329/ /pubmed/37162964 http://dx.doi.org/10.1101/2023.04.26.538446 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Gill, Nasiru K. Francis, Nikolas A. Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title | Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title_full | Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title_fullStr | Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title_full_unstemmed | Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title_short | Repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
title_sort | repetition plasticity in primary auditory cortex occurs across long timescales for spectrotemporally randomized pure-tones |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168329/ https://www.ncbi.nlm.nih.gov/pubmed/37162964 http://dx.doi.org/10.1101/2023.04.26.538446 |
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