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A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus
Accurately resolving frequency components in sounds is essential for sound recognition, yet there is little direct evidence for how frequency selectivity is preserved or newly created across auditory structures. We demonstrate that prepotentials (PPs) with physiological properties resembling presyna...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611646/ https://www.ncbi.nlm.nih.gov/pubmed/31233489 http://dx.doi.org/10.1371/journal.pbio.2005861 |
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author | Chen, Chen Read, Heather L. Escabí, Monty A. |
author_facet | Chen, Chen Read, Heather L. Escabí, Monty A. |
author_sort | Chen, Chen |
collection | PubMed |
description | Accurately resolving frequency components in sounds is essential for sound recognition, yet there is little direct evidence for how frequency selectivity is preserved or newly created across auditory structures. We demonstrate that prepotentials (PPs) with physiological properties resembling presynaptic potentials from broadly tuned brainstem inputs can be recorded concurrently with postsynaptic action potentials in inferior colliculus (IC). These putative brainstem inputs (PBIs) are broadly tuned and exhibit delayed and spectrally interleaved excitation and inhibition not present in the simultaneously recorded IC neurons (ICNs). A sharpening of tuning is accomplished locally at the expense of spike-timing precision through nonlinear temporal integration of broadband inputs. A neuron model replicates the finding and demonstrates that temporal integration alone can degrade timing precision while enhancing frequency tuning through interference of spectrally in- and out-of-phase inputs. These findings suggest that, in contrast to current models that require local inhibition, frequency selectivity can be sharpened through temporal integration, thus supporting an alternative computational strategy to quickly refine frequency selectivity. |
format | Online Article Text |
id | pubmed-6611646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66116462019-07-12 A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus Chen, Chen Read, Heather L. Escabí, Monty A. PLoS Biol Research Article Accurately resolving frequency components in sounds is essential for sound recognition, yet there is little direct evidence for how frequency selectivity is preserved or newly created across auditory structures. We demonstrate that prepotentials (PPs) with physiological properties resembling presynaptic potentials from broadly tuned brainstem inputs can be recorded concurrently with postsynaptic action potentials in inferior colliculus (IC). These putative brainstem inputs (PBIs) are broadly tuned and exhibit delayed and spectrally interleaved excitation and inhibition not present in the simultaneously recorded IC neurons (ICNs). A sharpening of tuning is accomplished locally at the expense of spike-timing precision through nonlinear temporal integration of broadband inputs. A neuron model replicates the finding and demonstrates that temporal integration alone can degrade timing precision while enhancing frequency tuning through interference of spectrally in- and out-of-phase inputs. These findings suggest that, in contrast to current models that require local inhibition, frequency selectivity can be sharpened through temporal integration, thus supporting an alternative computational strategy to quickly refine frequency selectivity. Public Library of Science 2019-06-24 /pmc/articles/PMC6611646/ /pubmed/31233489 http://dx.doi.org/10.1371/journal.pbio.2005861 Text en © 2019 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Chen Read, Heather L. Escabí, Monty A. A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title | A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title_full | A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title_fullStr | A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title_full_unstemmed | A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title_short | A temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
title_sort | temporal integration mechanism enhances frequency selectivity of broadband inputs to inferior colliculus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611646/ https://www.ncbi.nlm.nih.gov/pubmed/31233489 http://dx.doi.org/10.1371/journal.pbio.2005861 |
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