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Sensory experience during locomotion promotes recovery of function in adult visual cortex

Recovery from sensory deprivation is slow and incomplete in adult visual cortex. In this study, we show that visual stimulation during locomotion, which increases the gain of visual responses in primary visual cortex, dramatically enhances recovery in the mouse. Excitatory neurons regained normal le...

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Detalles Bibliográficos
Autores principales: Kaneko, Megumi, Stryker, Michael P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070284/
https://www.ncbi.nlm.nih.gov/pubmed/24970838
http://dx.doi.org/10.7554/eLife.02798
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author Kaneko, Megumi
Stryker, Michael P
author_facet Kaneko, Megumi
Stryker, Michael P
author_sort Kaneko, Megumi
collection PubMed
description Recovery from sensory deprivation is slow and incomplete in adult visual cortex. In this study, we show that visual stimulation during locomotion, which increases the gain of visual responses in primary visual cortex, dramatically enhances recovery in the mouse. Excitatory neurons regained normal levels of response, while narrow-spiking (inhibitory) neurons remained less active. Visual stimulation or locomotion alone did not enhance recovery. Responses to the particular visual stimuli viewed by the animal during locomotion recovered, while those to another normally effective stimulus did not, suggesting that locomotion promotes the recovery only of the neural circuits that are activated concurrent with the locomotion. These findings may provide an avenue for improving recovery from amblyopia in humans. DOI: http://dx.doi.org/10.7554/eLife.02798.001
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spelling pubmed-40702842014-06-27 Sensory experience during locomotion promotes recovery of function in adult visual cortex Kaneko, Megumi Stryker, Michael P eLife Neuroscience Recovery from sensory deprivation is slow and incomplete in adult visual cortex. In this study, we show that visual stimulation during locomotion, which increases the gain of visual responses in primary visual cortex, dramatically enhances recovery in the mouse. Excitatory neurons regained normal levels of response, while narrow-spiking (inhibitory) neurons remained less active. Visual stimulation or locomotion alone did not enhance recovery. Responses to the particular visual stimuli viewed by the animal during locomotion recovered, while those to another normally effective stimulus did not, suggesting that locomotion promotes the recovery only of the neural circuits that are activated concurrent with the locomotion. These findings may provide an avenue for improving recovery from amblyopia in humans. DOI: http://dx.doi.org/10.7554/eLife.02798.001 eLife Sciences Publications, Ltd 2014-06-26 /pmc/articles/PMC4070284/ /pubmed/24970838 http://dx.doi.org/10.7554/eLife.02798 Text en Copyright © 2014, Kaneko and Stryker http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Kaneko, Megumi
Stryker, Michael P
Sensory experience during locomotion promotes recovery of function in adult visual cortex
title Sensory experience during locomotion promotes recovery of function in adult visual cortex
title_full Sensory experience during locomotion promotes recovery of function in adult visual cortex
title_fullStr Sensory experience during locomotion promotes recovery of function in adult visual cortex
title_full_unstemmed Sensory experience during locomotion promotes recovery of function in adult visual cortex
title_short Sensory experience during locomotion promotes recovery of function in adult visual cortex
title_sort sensory experience during locomotion promotes recovery of function in adult visual cortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070284/
https://www.ncbi.nlm.nih.gov/pubmed/24970838
http://dx.doi.org/10.7554/eLife.02798
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