Cargando…
Self-motion evokes precise spike timing in the primate vestibular system
The accurate representation of self-motion requires the efficient processing of sensory input by the vestibular system. Conventional wisdom is that vestibular information is exclusively transmitted through changes in firing rate, yet under this assumption vestibular neurons display relatively poor d...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095295/ https://www.ncbi.nlm.nih.gov/pubmed/27786265 http://dx.doi.org/10.1038/ncomms13229 |
_version_ | 1782465278230134784 |
---|---|
author | Jamali, Mohsen Chacron, Maurice J. Cullen, Kathleen E. |
author_facet | Jamali, Mohsen Chacron, Maurice J. Cullen, Kathleen E. |
author_sort | Jamali, Mohsen |
collection | PubMed |
description | The accurate representation of self-motion requires the efficient processing of sensory input by the vestibular system. Conventional wisdom is that vestibular information is exclusively transmitted through changes in firing rate, yet under this assumption vestibular neurons display relatively poor detection and information transmission. Here, we carry out an analysis of the system's coding capabilities by recording neuronal responses to repeated presentations of naturalistic stimuli. We find that afferents with greater intrinsic variability reliably discriminate between different stimulus waveforms through differential patterns of precise (∼6 ms) spike timing, while those with minimal intrinsic variability do not. A simple mathematical model provides an explanation for this result. Postsynaptic central neurons also demonstrate precise spike timing, suggesting that higher brain areas also represent self-motion using temporally precise firing. These findings demonstrate that two distinct sensory channels represent vestibular information: one using rate coding and the other that takes advantage of precise spike timing. |
format | Online Article Text |
id | pubmed-5095295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50952952016-11-18 Self-motion evokes precise spike timing in the primate vestibular system Jamali, Mohsen Chacron, Maurice J. Cullen, Kathleen E. Nat Commun Article The accurate representation of self-motion requires the efficient processing of sensory input by the vestibular system. Conventional wisdom is that vestibular information is exclusively transmitted through changes in firing rate, yet under this assumption vestibular neurons display relatively poor detection and information transmission. Here, we carry out an analysis of the system's coding capabilities by recording neuronal responses to repeated presentations of naturalistic stimuli. We find that afferents with greater intrinsic variability reliably discriminate between different stimulus waveforms through differential patterns of precise (∼6 ms) spike timing, while those with minimal intrinsic variability do not. A simple mathematical model provides an explanation for this result. Postsynaptic central neurons also demonstrate precise spike timing, suggesting that higher brain areas also represent self-motion using temporally precise firing. These findings demonstrate that two distinct sensory channels represent vestibular information: one using rate coding and the other that takes advantage of precise spike timing. Nature Publishing Group 2016-10-27 /pmc/articles/PMC5095295/ /pubmed/27786265 http://dx.doi.org/10.1038/ncomms13229 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jamali, Mohsen Chacron, Maurice J. Cullen, Kathleen E. Self-motion evokes precise spike timing in the primate vestibular system |
title | Self-motion evokes precise spike timing in the primate vestibular system |
title_full | Self-motion evokes precise spike timing in the primate vestibular system |
title_fullStr | Self-motion evokes precise spike timing in the primate vestibular system |
title_full_unstemmed | Self-motion evokes precise spike timing in the primate vestibular system |
title_short | Self-motion evokes precise spike timing in the primate vestibular system |
title_sort | self-motion evokes precise spike timing in the primate vestibular system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095295/ https://www.ncbi.nlm.nih.gov/pubmed/27786265 http://dx.doi.org/10.1038/ncomms13229 |
work_keys_str_mv | AT jamalimohsen selfmotionevokesprecisespiketimingintheprimatevestibularsystem AT chacronmauricej selfmotionevokesprecisespiketimingintheprimatevestibularsystem AT cullenkathleene selfmotionevokesprecisespiketimingintheprimatevestibularsystem |