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Laminar profile of task-related plasticity in ferret primary auditory cortex
Rapid task-related plasticity is a neural correlate of selective attention in primary auditory cortex (A1). Top-down feedback from higher-order cortex may drive task-related plasticity in A1, characterized by enhanced neural representation of behaviorally meaningful sounds during auditory task perfo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219524/ https://www.ncbi.nlm.nih.gov/pubmed/30401927 http://dx.doi.org/10.1038/s41598-018-34739-3 |
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author | Francis, Nikolas A. Elgueda, Diego Englitz, Bernhard Fritz, Jonathan B. Shamma, Shihab A. |
author_facet | Francis, Nikolas A. Elgueda, Diego Englitz, Bernhard Fritz, Jonathan B. Shamma, Shihab A. |
author_sort | Francis, Nikolas A. |
collection | PubMed |
description | Rapid task-related plasticity is a neural correlate of selective attention in primary auditory cortex (A1). Top-down feedback from higher-order cortex may drive task-related plasticity in A1, characterized by enhanced neural representation of behaviorally meaningful sounds during auditory task performance. Since intracortical connectivity is greater within A1 layers 2/3 (L2/3) than in layers 4–6 (L4–6), we hypothesized that enhanced representation of behaviorally meaningful sounds might be greater in A1 L2/3 than L4–6. To test this hypothesis and study the laminar profile of task-related plasticity, we trained 2 ferrets to detect pure tones while we recorded laminar activity across a 1.8 mm depth in A1. In each experiment we analyzed high-gamma local field potentials (LFPs) and multi-unit spiking in response to identical acoustic stimuli during both passive listening and active task performance. We found that neural responses to auditory targets were enhanced during task performance, and target enhancement was greater in L2/3 than in L4–6. Spectrotemporal receptive fields (STRFs) computed from both high-gamma LFPs and multi-unit spiking showed similar increases in auditory target selectivity, also greatest in L2/3. Our results suggest that activity within intracortical networks plays a key role in the underlying neural mechanisms of selective attention. |
format | Online Article Text |
id | pubmed-6219524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62195242018-11-07 Laminar profile of task-related plasticity in ferret primary auditory cortex Francis, Nikolas A. Elgueda, Diego Englitz, Bernhard Fritz, Jonathan B. Shamma, Shihab A. Sci Rep Article Rapid task-related plasticity is a neural correlate of selective attention in primary auditory cortex (A1). Top-down feedback from higher-order cortex may drive task-related plasticity in A1, characterized by enhanced neural representation of behaviorally meaningful sounds during auditory task performance. Since intracortical connectivity is greater within A1 layers 2/3 (L2/3) than in layers 4–6 (L4–6), we hypothesized that enhanced representation of behaviorally meaningful sounds might be greater in A1 L2/3 than L4–6. To test this hypothesis and study the laminar profile of task-related plasticity, we trained 2 ferrets to detect pure tones while we recorded laminar activity across a 1.8 mm depth in A1. In each experiment we analyzed high-gamma local field potentials (LFPs) and multi-unit spiking in response to identical acoustic stimuli during both passive listening and active task performance. We found that neural responses to auditory targets were enhanced during task performance, and target enhancement was greater in L2/3 than in L4–6. Spectrotemporal receptive fields (STRFs) computed from both high-gamma LFPs and multi-unit spiking showed similar increases in auditory target selectivity, also greatest in L2/3. Our results suggest that activity within intracortical networks plays a key role in the underlying neural mechanisms of selective attention. Nature Publishing Group UK 2018-11-06 /pmc/articles/PMC6219524/ /pubmed/30401927 http://dx.doi.org/10.1038/s41598-018-34739-3 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Francis, Nikolas A. Elgueda, Diego Englitz, Bernhard Fritz, Jonathan B. Shamma, Shihab A. Laminar profile of task-related plasticity in ferret primary auditory cortex |
title | Laminar profile of task-related plasticity in ferret primary auditory cortex |
title_full | Laminar profile of task-related plasticity in ferret primary auditory cortex |
title_fullStr | Laminar profile of task-related plasticity in ferret primary auditory cortex |
title_full_unstemmed | Laminar profile of task-related plasticity in ferret primary auditory cortex |
title_short | Laminar profile of task-related plasticity in ferret primary auditory cortex |
title_sort | laminar profile of task-related plasticity in ferret primary auditory cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219524/ https://www.ncbi.nlm.nih.gov/pubmed/30401927 http://dx.doi.org/10.1038/s41598-018-34739-3 |
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