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Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion

The recruitment of additional neurons to neural circuits often occurs in accordance with changing functional demands. Here we found that synaptic recruitment plays a key role in functional recovery after neural injury. Disconnection of a brain commissure in the nudibranch mollusc, Tritonia diomedea,...

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Autores principales: Sakurai, Akira, Tamvacakis, Arianna N., Katz, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999536/
https://www.ncbi.nlm.nih.gov/pubmed/27570828
http://dx.doi.org/10.1523/ENEURO.0056-16.2016
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author Sakurai, Akira
Tamvacakis, Arianna N.
Katz, Paul S.
author_facet Sakurai, Akira
Tamvacakis, Arianna N.
Katz, Paul S.
author_sort Sakurai, Akira
collection PubMed
description The recruitment of additional neurons to neural circuits often occurs in accordance with changing functional demands. Here we found that synaptic recruitment plays a key role in functional recovery after neural injury. Disconnection of a brain commissure in the nudibranch mollusc, Tritonia diomedea, impairs swimming behavior by eliminating particular synapses in the central pattern generator (CPG) underlying the rhythmic swim motor pattern. However, the CPG functionally recovers within a day after the lesion. The strength of a spared inhibitory synapse within the CPG from Cerebral Neuron 2 (C2) to Ventral Swim Interneuron B (VSI) determines the level of impairment caused by the lesion, which varies among individuals. In addition to this direct synaptic connection, there are polysynaptic connections from C2 and Dorsal Swim Interneurons to VSI that provide indirect excitatory drive but play only minor roles under normal conditions. After disconnecting the pedal commissure (Pedal Nerve 6), the recruitment of polysynaptic excitation became a major source of the excitatory drive to VSI. Moreover, the amount of polysynaptic recruitment, which changed over time, differed among individuals and correlated with the degree of recovery of the swim motor pattern. Thus, functional recovery was mediated by an increase in the magnitude of polysynaptic excitatory drive, compensating for the loss of direct excitation. Since the degree of susceptibility to injury corresponds to existing individual variation in the C2 to VSI synapse, the recovery relied upon the extent to which the network reorganized to incorporate additional synapses.
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spelling pubmed-49995362016-08-26 Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion Sakurai, Akira Tamvacakis, Arianna N. Katz, Paul S. eNeuro New Research The recruitment of additional neurons to neural circuits often occurs in accordance with changing functional demands. Here we found that synaptic recruitment plays a key role in functional recovery after neural injury. Disconnection of a brain commissure in the nudibranch mollusc, Tritonia diomedea, impairs swimming behavior by eliminating particular synapses in the central pattern generator (CPG) underlying the rhythmic swim motor pattern. However, the CPG functionally recovers within a day after the lesion. The strength of a spared inhibitory synapse within the CPG from Cerebral Neuron 2 (C2) to Ventral Swim Interneuron B (VSI) determines the level of impairment caused by the lesion, which varies among individuals. In addition to this direct synaptic connection, there are polysynaptic connections from C2 and Dorsal Swim Interneurons to VSI that provide indirect excitatory drive but play only minor roles under normal conditions. After disconnecting the pedal commissure (Pedal Nerve 6), the recruitment of polysynaptic excitation became a major source of the excitatory drive to VSI. Moreover, the amount of polysynaptic recruitment, which changed over time, differed among individuals and correlated with the degree of recovery of the swim motor pattern. Thus, functional recovery was mediated by an increase in the magnitude of polysynaptic excitatory drive, compensating for the loss of direct excitation. Since the degree of susceptibility to injury corresponds to existing individual variation in the C2 to VSI synapse, the recovery relied upon the extent to which the network reorganized to incorporate additional synapses. Society for Neuroscience 2016-08-26 /pmc/articles/PMC4999536/ /pubmed/27570828 http://dx.doi.org/10.1523/ENEURO.0056-16.2016 Text en Copyright © 2016 Sakurai et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Sakurai, Akira
Tamvacakis, Arianna N.
Katz, Paul S.
Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title_full Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title_fullStr Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title_full_unstemmed Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title_short Recruitment of Polysynaptic Connections Underlies Functional Recovery of a Neural Circuit after Lesion
title_sort recruitment of polysynaptic connections underlies functional recovery of a neural circuit after lesion
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999536/
https://www.ncbi.nlm.nih.gov/pubmed/27570828
http://dx.doi.org/10.1523/ENEURO.0056-16.2016
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