Cargando…
Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo
Although cerebellar mechanisms are vital to maintain accuracy during complex movements and to calibrate simple reflexes, recent in vitro studies have called into question the widely held view that synaptic changes within cerebellar pathways exclusively guide alterations in motor performance. Here we...
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/PMC4865756/ https://www.ncbi.nlm.nih.gov/pubmed/27157829 http://dx.doi.org/10.1038/ncomms11238 |
_version_ | 1782431830224404480 |
---|---|
author | Mitchell, Diana E. Della Santina, Charles C. Cullen, Kathleen E. |
author_facet | Mitchell, Diana E. Della Santina, Charles C. Cullen, Kathleen E. |
author_sort | Mitchell, Diana E. |
collection | PubMed |
description | Although cerebellar mechanisms are vital to maintain accuracy during complex movements and to calibrate simple reflexes, recent in vitro studies have called into question the widely held view that synaptic changes within cerebellar pathways exclusively guide alterations in motor performance. Here we investigate the vestibulo-ocular reflex (VOR) circuitry by applying temporally precise activation of vestibular afferents in awake-behaving monkeys to link plasticity at different neural sites with changes in motor performance. Behaviourally relevant activation patterns produce rapid attenuation of direct pathway VOR neurons, but not their nerve input. Changes in the strength of this pathway are sufficient to induce a lasting decrease in the evoked VOR. In addition, indirect brainstem pathways display complementary nearly instantaneous changes, contributing to compensating for the reduced sensitivity of primary VOR neurons. Taken together, our data provide evidence that multiple sites of plasticity within VOR pathways can rapidly shape motor performance in vivo. |
format | Online Article Text |
id | pubmed-4865756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48657562016-05-24 Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo Mitchell, Diana E. Della Santina, Charles C. Cullen, Kathleen E. Nat Commun Article Although cerebellar mechanisms are vital to maintain accuracy during complex movements and to calibrate simple reflexes, recent in vitro studies have called into question the widely held view that synaptic changes within cerebellar pathways exclusively guide alterations in motor performance. Here we investigate the vestibulo-ocular reflex (VOR) circuitry by applying temporally precise activation of vestibular afferents in awake-behaving monkeys to link plasticity at different neural sites with changes in motor performance. Behaviourally relevant activation patterns produce rapid attenuation of direct pathway VOR neurons, but not their nerve input. Changes in the strength of this pathway are sufficient to induce a lasting decrease in the evoked VOR. In addition, indirect brainstem pathways display complementary nearly instantaneous changes, contributing to compensating for the reduced sensitivity of primary VOR neurons. Taken together, our data provide evidence that multiple sites of plasticity within VOR pathways can rapidly shape motor performance in vivo. Nature Publishing Group 2016-05-09 /pmc/articles/PMC4865756/ /pubmed/27157829 http://dx.doi.org/10.1038/ncomms11238 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Mitchell, Diana E. Della Santina, Charles C. Cullen, Kathleen E. Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title | Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title_full | Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title_fullStr | Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title_full_unstemmed | Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title_short | Plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
title_sort | plasticity within non-cerebellar pathways rapidly shapes motor performance in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865756/ https://www.ncbi.nlm.nih.gov/pubmed/27157829 http://dx.doi.org/10.1038/ncomms11238 |
work_keys_str_mv | AT mitchelldianae plasticitywithinnoncerebellarpathwaysrapidlyshapesmotorperformanceinvivo AT dellasantinacharlesc plasticitywithinnoncerebellarpathwaysrapidlyshapesmotorperformanceinvivo AT cullenkathleene plasticitywithinnoncerebellarpathwaysrapidlyshapesmotorperformanceinvivo |