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Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem
The integration of excitatory and inhibitory synaptic inputs is fundamental to neuronal processing. In the mammalian auditory brainstem, neurons compare excitatory and inhibitory inputs from the ipsilateral and contralateral ear, respectively, for sound localization. However, the temporal precision...
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/PMC5932051/ https://www.ncbi.nlm.nih.gov/pubmed/29720589 http://dx.doi.org/10.1038/s41467-018-04210-y |
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author | Beiderbeck, Barbara Myoga, Michael H. Müller, Nicolas I. C. Callan, Alexander R. Friauf, Eckhard Grothe, Benedikt Pecka, Michael |
author_facet | Beiderbeck, Barbara Myoga, Michael H. Müller, Nicolas I. C. Callan, Alexander R. Friauf, Eckhard Grothe, Benedikt Pecka, Michael |
author_sort | Beiderbeck, Barbara |
collection | PubMed |
description | The integration of excitatory and inhibitory synaptic inputs is fundamental to neuronal processing. In the mammalian auditory brainstem, neurons compare excitatory and inhibitory inputs from the ipsilateral and contralateral ear, respectively, for sound localization. However, the temporal precision and functional roles of inhibition in this integration process are unclear. Here, we demonstrate by in vivo recordings from the lateral superior olive (LSO) that inhibition controls spiking with microsecond precision throughout high frequency click trains. Depending on the relative timing of excitation and inhibition, neuronal spike probability is either suppressed or—unexpectedly—facilitated. In vitro conductance-clamp LSO recordings establish that a reduction in the voltage threshold for spike initiation due to a prior hyperpolarization results in post-inhibitory facilitation of otherwise sub-threshold synaptic events. Thus, microsecond-precise differences in the arrival of inhibition relative to excitation can facilitate spiking in the LSO, thereby promoting spatial sensitivity during the processing of faint sounds. |
format | Online Article Text |
id | pubmed-5932051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59320512018-05-07 Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem Beiderbeck, Barbara Myoga, Michael H. Müller, Nicolas I. C. Callan, Alexander R. Friauf, Eckhard Grothe, Benedikt Pecka, Michael Nat Commun Article The integration of excitatory and inhibitory synaptic inputs is fundamental to neuronal processing. In the mammalian auditory brainstem, neurons compare excitatory and inhibitory inputs from the ipsilateral and contralateral ear, respectively, for sound localization. However, the temporal precision and functional roles of inhibition in this integration process are unclear. Here, we demonstrate by in vivo recordings from the lateral superior olive (LSO) that inhibition controls spiking with microsecond precision throughout high frequency click trains. Depending on the relative timing of excitation and inhibition, neuronal spike probability is either suppressed or—unexpectedly—facilitated. In vitro conductance-clamp LSO recordings establish that a reduction in the voltage threshold for spike initiation due to a prior hyperpolarization results in post-inhibitory facilitation of otherwise sub-threshold synaptic events. Thus, microsecond-precise differences in the arrival of inhibition relative to excitation can facilitate spiking in the LSO, thereby promoting spatial sensitivity during the processing of faint sounds. Nature Publishing Group UK 2018-05-02 /pmc/articles/PMC5932051/ /pubmed/29720589 http://dx.doi.org/10.1038/s41467-018-04210-y 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 Beiderbeck, Barbara Myoga, Michael H. Müller, Nicolas I. C. Callan, Alexander R. Friauf, Eckhard Grothe, Benedikt Pecka, Michael Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title | Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title_full | Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title_fullStr | Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title_full_unstemmed | Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title_short | Precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
title_sort | precisely timed inhibition facilitates action potential firing for spatial coding in the auditory brainstem |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932051/ https://www.ncbi.nlm.nih.gov/pubmed/29720589 http://dx.doi.org/10.1038/s41467-018-04210-y |
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