Cargando…
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,...
Autores principales: | , , |
---|---|
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 |
_version_ | 1782450140528771072 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4999536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sakuraiakira recruitmentofpolysynapticconnectionsunderliesfunctionalrecoveryofaneuralcircuitafterlesion AT tamvacakisariannan recruitmentofpolysynapticconnectionsunderliesfunctionalrecoveryofaneuralcircuitafterlesion AT katzpauls recruitmentofpolysynapticconnectionsunderliesfunctionalrecoveryofaneuralcircuitafterlesion |