Cargando…
The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
Spike trains are rich in information that can be extracted to guide behaviors at millisecond time resolution or across longer time intervals. In sensory systems, the information usually is defined with respect to the stimulus. Especially in motor systems, however, it is equally critical to understan...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596133/ https://www.ncbi.nlm.nih.gov/pubmed/26464956 http://dx.doi.org/10.1523/ENEURO.0004-14.2014 |
_version_ | 1782393725661478912 |
---|---|
author | Chaisanguanthum, Kris S. Joshua, Mati Medina, Javier F. Bialek, William Lisberger, Stephen G. |
author_facet | Chaisanguanthum, Kris S. Joshua, Mati Medina, Javier F. Bialek, William Lisberger, Stephen G. |
author_sort | Chaisanguanthum, Kris S. |
collection | PubMed |
description | Spike trains are rich in information that can be extracted to guide behaviors at millisecond time resolution or across longer time intervals. In sensory systems, the information usually is defined with respect to the stimulus. Especially in motor systems, however, it is equally critical to understand how spike trains predict behavior. Thus, our goal was to compare systematically spike trains in the oculomotor system with eye movement behavior on single movements. We analyzed the discharge of Purkinje cells in the floccular complex of the cerebellum, floccular target neurons in the brainstem, other vestibular neurons, and abducens neurons. We find that an extra spike in a brief analysis window predicts a substantial fraction of the trial-by-trial variation in the initiation of smooth pursuit eye movements. For Purkinje cells, a single extra spike in a 40 ms analysis window predicts, on average, 0.5 SDs of the variation in behavior. An optimal linear estimator predicts behavioral variation slightly better than do spike counts in brief windows. Simulations reveal that the ability of single spikes to predict a fraction of behavior also emerges from model spike trains that have the same statistics as the real spike trains, as long as they are driven by shared sensory inputs. We think that the shared sensory estimates in their inputs create correlations in neural spiking across time and across each population. As a result, one or a small number of spikes in a brief time interval can predict a substantial fraction of behavioral variation. |
format | Online Article Text |
id | pubmed-4596133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-45961332015-10-13 The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡ Chaisanguanthum, Kris S. Joshua, Mati Medina, Javier F. Bialek, William Lisberger, Stephen G. eNeuro New Research Spike trains are rich in information that can be extracted to guide behaviors at millisecond time resolution or across longer time intervals. In sensory systems, the information usually is defined with respect to the stimulus. Especially in motor systems, however, it is equally critical to understand how spike trains predict behavior. Thus, our goal was to compare systematically spike trains in the oculomotor system with eye movement behavior on single movements. We analyzed the discharge of Purkinje cells in the floccular complex of the cerebellum, floccular target neurons in the brainstem, other vestibular neurons, and abducens neurons. We find that an extra spike in a brief analysis window predicts a substantial fraction of the trial-by-trial variation in the initiation of smooth pursuit eye movements. For Purkinje cells, a single extra spike in a 40 ms analysis window predicts, on average, 0.5 SDs of the variation in behavior. An optimal linear estimator predicts behavioral variation slightly better than do spike counts in brief windows. Simulations reveal that the ability of single spikes to predict a fraction of behavior also emerges from model spike trains that have the same statistics as the real spike trains, as long as they are driven by shared sensory inputs. We think that the shared sensory estimates in their inputs create correlations in neural spiking across time and across each population. As a result, one or a small number of spikes in a brief time interval can predict a substantial fraction of behavioral variation. Society for Neuroscience 2014-11-12 /pmc/articles/PMC4596133/ /pubmed/26464956 http://dx.doi.org/10.1523/ENEURO.0004-14.2014 Text en Copyright © 2014 Chaisanguanthum et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License Attribution-Noncommercial 4.0 International (http://creativecommons.org/licenses/by-nc/4.0/) which permits noncommercial reuse provided that the original work is properly attributed. |
spellingShingle | New Research Chaisanguanthum, Kris S. Joshua, Mati Medina, Javier F. Bialek, William Lisberger, Stephen G. The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡ |
title | The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
|
title_full | The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
|
title_fullStr | The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
|
title_full_unstemmed | The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
|
title_short | The Neural Code for Motor Control in the Cerebellum and Oculomotor Brainstem†‡
|
title_sort | neural code for motor control in the cerebellum and oculomotor brainstem†‡ |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596133/ https://www.ncbi.nlm.nih.gov/pubmed/26464956 http://dx.doi.org/10.1523/ENEURO.0004-14.2014 |
work_keys_str_mv | AT chaisanguanthumkriss theneuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT joshuamati theneuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT medinajavierf theneuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT bialekwilliam theneuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT lisbergerstepheng theneuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT chaisanguanthumkriss neuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT joshuamati neuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT medinajavierf neuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT bialekwilliam neuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem AT lisbergerstepheng neuralcodeformotorcontrolinthecerebellumandoculomotorbrainstem |