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Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics

The neural dynamics of the nematode Caenorhabditis elegans are experimentally low-dimensional and may be understood as long-timescale transitions between multiple low-dimensional attractors. Previous modeling work has found that dynamic models of the worm's full neuronal network are capable of...

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Autores principales: Kunert-Graf, James M., Shlizerman, Eli, Walker, Andrew, Kutz, J. Nathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468412/
https://www.ncbi.nlm.nih.gov/pubmed/28659783
http://dx.doi.org/10.3389/fncom.2017.00053
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author Kunert-Graf, James M.
Shlizerman, Eli
Walker, Andrew
Kutz, J. Nathan
author_facet Kunert-Graf, James M.
Shlizerman, Eli
Walker, Andrew
Kutz, J. Nathan
author_sort Kunert-Graf, James M.
collection PubMed
description The neural dynamics of the nematode Caenorhabditis elegans are experimentally low-dimensional and may be understood as long-timescale transitions between multiple low-dimensional attractors. Previous modeling work has found that dynamic models of the worm's full neuronal network are capable of generating reasonable dynamic responses to certain inputs, even when all neurons are treated as identical save for their connectivity. This study investigates such a model of C. elegans neuronal dynamics, finding that a wide variety of multistable responses are generated in response to varied inputs. Specifically, we generate bifurcation diagrams for all possible single-neuron inputs, showing the existence of fixed points and limit cycles for different input regimes. The nature of the dynamical response is seen to vary according to the type of neuron receiving input; for example, input into sensory neurons is more likely to drive a bifurcation in the system than input into motor neurons. As a specific example we consider compound input into the neuron pairs PLM and ASK, discovering bistability of a limit cycle and a fixed point. The transient timescales in approaching each of these states are much longer than any intrinsic timescales of the system. This suggests consistency of our model with the characterization of dynamics in neural systems as long-timescale transitions between discrete, low-dimensional attractors corresponding to behavioral states.
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spelling pubmed-54684122017-06-28 Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics Kunert-Graf, James M. Shlizerman, Eli Walker, Andrew Kutz, J. Nathan Front Comput Neurosci Neuroscience The neural dynamics of the nematode Caenorhabditis elegans are experimentally low-dimensional and may be understood as long-timescale transitions between multiple low-dimensional attractors. Previous modeling work has found that dynamic models of the worm's full neuronal network are capable of generating reasonable dynamic responses to certain inputs, even when all neurons are treated as identical save for their connectivity. This study investigates such a model of C. elegans neuronal dynamics, finding that a wide variety of multistable responses are generated in response to varied inputs. Specifically, we generate bifurcation diagrams for all possible single-neuron inputs, showing the existence of fixed points and limit cycles for different input regimes. The nature of the dynamical response is seen to vary according to the type of neuron receiving input; for example, input into sensory neurons is more likely to drive a bifurcation in the system than input into motor neurons. As a specific example we consider compound input into the neuron pairs PLM and ASK, discovering bistability of a limit cycle and a fixed point. The transient timescales in approaching each of these states are much longer than any intrinsic timescales of the system. This suggests consistency of our model with the characterization of dynamics in neural systems as long-timescale transitions between discrete, low-dimensional attractors corresponding to behavioral states. Frontiers Media S.A. 2017-06-13 /pmc/articles/PMC5468412/ /pubmed/28659783 http://dx.doi.org/10.3389/fncom.2017.00053 Text en Copyright © 2017 Kunert-Graf, Shlizerman, Walker and Kutz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Kunert-Graf, James M.
Shlizerman, Eli
Walker, Andrew
Kutz, J. Nathan
Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title_full Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title_fullStr Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title_full_unstemmed Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title_short Multistability and Long-Timescale Transients Encoded by Network Structure in a Model of C. elegans Connectome Dynamics
title_sort multistability and long-timescale transients encoded by network structure in a model of c. elegans connectome dynamics
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468412/
https://www.ncbi.nlm.nih.gov/pubmed/28659783
http://dx.doi.org/10.3389/fncom.2017.00053
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