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Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice

Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse...

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Autores principales: Bellardita, Carmelo, Caggiano, Vittorio, Leiras, Roberto, Caldeira, Vanessa, Fuchs, Andrea, Bouvier, Julien, Löw, Peter, Kiehn, Ole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332159/
https://www.ncbi.nlm.nih.gov/pubmed/28191872
http://dx.doi.org/10.7554/eLife.23011
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author Bellardita, Carmelo
Caggiano, Vittorio
Leiras, Roberto
Caldeira, Vanessa
Fuchs, Andrea
Bouvier, Julien
Löw, Peter
Kiehn, Ole
author_facet Bellardita, Carmelo
Caggiano, Vittorio
Leiras, Roberto
Caldeira, Vanessa
Fuchs, Andrea
Bouvier, Julien
Löw, Peter
Kiehn, Ole
author_sort Bellardita, Carmelo
collection PubMed
description Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse genetics, electrophysiology, imaging and optogenetics to directly target major classes of spinal interneurons as well as motor neurons during spasms in a mouse model of chronic SCI. We find that assemblies of excitatory spinal interneurons are recruited by sensory input into functional circuits to generate persistent neural activity, which interacts with both the graded expression of plateau potentials in motor neurons to generate spasms, and inhibitory interneurons to curtail them. Our study reveals hitherto unrecognized neuronal mechanisms for the generation of persistent neural activity under pathophysiological conditions, opening up new targets for treatment of muscle spasms after SCI. DOI: http://dx.doi.org/10.7554/eLife.23011.001
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spelling pubmed-53321592017-03-02 Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice Bellardita, Carmelo Caggiano, Vittorio Leiras, Roberto Caldeira, Vanessa Fuchs, Andrea Bouvier, Julien Löw, Peter Kiehn, Ole eLife Neuroscience Spasms after spinal cord injury (SCI) are debilitating involuntary muscle contractions that have been associated with increased motor neuron excitability and decreased inhibition. However, whether spasms involve activation of premotor spinal excitatory neuronal circuits is unknown. Here we use mouse genetics, electrophysiology, imaging and optogenetics to directly target major classes of spinal interneurons as well as motor neurons during spasms in a mouse model of chronic SCI. We find that assemblies of excitatory spinal interneurons are recruited by sensory input into functional circuits to generate persistent neural activity, which interacts with both the graded expression of plateau potentials in motor neurons to generate spasms, and inhibitory interneurons to curtail them. Our study reveals hitherto unrecognized neuronal mechanisms for the generation of persistent neural activity under pathophysiological conditions, opening up new targets for treatment of muscle spasms after SCI. DOI: http://dx.doi.org/10.7554/eLife.23011.001 eLife Sciences Publications, Ltd 2017-02-13 /pmc/articles/PMC5332159/ /pubmed/28191872 http://dx.doi.org/10.7554/eLife.23011 Text en © 2017, Bellardita et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Bellardita, Carmelo
Caggiano, Vittorio
Leiras, Roberto
Caldeira, Vanessa
Fuchs, Andrea
Bouvier, Julien
Löw, Peter
Kiehn, Ole
Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title_full Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title_fullStr Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title_full_unstemmed Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title_short Spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
title_sort spatiotemporal correlation of spinal network dynamics underlying spasms in chronic spinalized mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5332159/
https://www.ncbi.nlm.nih.gov/pubmed/28191872
http://dx.doi.org/10.7554/eLife.23011
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