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Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network
Motor neurons of the crustacean cardiac ganglion generate virtually identical, synchronized output despite the fact that each neuron uses distinct conductance magnitudes. As a result of this variability, manipulations that target ionic conductances have distinct effects on neurons within the same ga...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026470/ https://www.ncbi.nlm.nih.gov/pubmed/27552052 http://dx.doi.org/10.7554/eLife.16879 |
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author | Lane, Brian J Samarth, Pranit Ransdell, Joseph L Nair, Satish S Schulz, David J |
author_facet | Lane, Brian J Samarth, Pranit Ransdell, Joseph L Nair, Satish S Schulz, David J |
author_sort | Lane, Brian J |
collection | PubMed |
description | Motor neurons of the crustacean cardiac ganglion generate virtually identical, synchronized output despite the fact that each neuron uses distinct conductance magnitudes. As a result of this variability, manipulations that target ionic conductances have distinct effects on neurons within the same ganglion, disrupting synchronized motor neuron output that is necessary for proper cardiac function. We hypothesized that robustness in network output is accomplished via plasticity that counters such destabilizing influences. By blocking high-threshold K(+) conductances in motor neurons within the ongoing cardiac network, we discovered that compensation both resynchronized the network and helped restore excitability. Using model findings to guide experimentation, we determined that compensatory increases of both G(A) and electrical coupling restored function in the network. This is one of the first direct demonstrations of the physiological regulation of coupling conductance in a compensatory context, and of synergistic plasticity across cell- and network-level mechanisms in the restoration of output. DOI: http://dx.doi.org/10.7554/eLife.16879.001 |
format | Online Article Text |
id | pubmed-5026470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50264702016-09-20 Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network Lane, Brian J Samarth, Pranit Ransdell, Joseph L Nair, Satish S Schulz, David J eLife Neuroscience Motor neurons of the crustacean cardiac ganglion generate virtually identical, synchronized output despite the fact that each neuron uses distinct conductance magnitudes. As a result of this variability, manipulations that target ionic conductances have distinct effects on neurons within the same ganglion, disrupting synchronized motor neuron output that is necessary for proper cardiac function. We hypothesized that robustness in network output is accomplished via plasticity that counters such destabilizing influences. By blocking high-threshold K(+) conductances in motor neurons within the ongoing cardiac network, we discovered that compensation both resynchronized the network and helped restore excitability. Using model findings to guide experimentation, we determined that compensatory increases of both G(A) and electrical coupling restored function in the network. This is one of the first direct demonstrations of the physiological regulation of coupling conductance in a compensatory context, and of synergistic plasticity across cell- and network-level mechanisms in the restoration of output. DOI: http://dx.doi.org/10.7554/eLife.16879.001 eLife Sciences Publications, Ltd 2016-08-23 /pmc/articles/PMC5026470/ /pubmed/27552052 http://dx.doi.org/10.7554/eLife.16879 Text en © 2016, Lane 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 Lane, Brian J Samarth, Pranit Ransdell, Joseph L Nair, Satish S Schulz, David J Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title | Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title_full | Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title_fullStr | Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title_full_unstemmed | Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title_short | Synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
title_sort | synergistic plasticity of intrinsic conductance and electrical coupling restores synchrony in an intact motor network |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026470/ https://www.ncbi.nlm.nih.gov/pubmed/27552052 http://dx.doi.org/10.7554/eLife.16879 |
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