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A quantitative model of conserved macroscopic dynamics predicts future motor commands

In simple organisms such as Caenorhabditis elegans, whole brain imaging has been performed. Here, we use such recordings to model the nervous system. Our model uses neuronal activity to predict expected time of future motor commands up to 30 s prior to the event. These motor commands control locomot...

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Detalles Bibliográficos
Autores principales: Brennan, Connor, Proekt, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624016/
https://www.ncbi.nlm.nih.gov/pubmed/31294689
http://dx.doi.org/10.7554/eLife.46814
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author Brennan, Connor
Proekt, Alexander
author_facet Brennan, Connor
Proekt, Alexander
author_sort Brennan, Connor
collection PubMed
description In simple organisms such as Caenorhabditis elegans, whole brain imaging has been performed. Here, we use such recordings to model the nervous system. Our model uses neuronal activity to predict expected time of future motor commands up to 30 s prior to the event. These motor commands control locomotion. Predictions are valid for individuals not used in model construction. The model predicts dwell time statistics, sequences of motor commands and individual neuron activation. To develop this model, we extracted loops spanned by neuronal activity in phase space using novel methodology. The model uses only two variables: the identity of the loop and the phase along it. Current values of these macroscopic variables predict future neuronal activity. Remarkably, our model based on macroscopic variables succeeds despite consistent inter-individual differences in neuronal activation. Thus, our analytical framework reconciles consistent individual differences in neuronal activation with macroscopic dynamics that operate universally across individuals.
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spelling pubmed-66240162019-07-12 A quantitative model of conserved macroscopic dynamics predicts future motor commands Brennan, Connor Proekt, Alexander eLife Computational and Systems Biology In simple organisms such as Caenorhabditis elegans, whole brain imaging has been performed. Here, we use such recordings to model the nervous system. Our model uses neuronal activity to predict expected time of future motor commands up to 30 s prior to the event. These motor commands control locomotion. Predictions are valid for individuals not used in model construction. The model predicts dwell time statistics, sequences of motor commands and individual neuron activation. To develop this model, we extracted loops spanned by neuronal activity in phase space using novel methodology. The model uses only two variables: the identity of the loop and the phase along it. Current values of these macroscopic variables predict future neuronal activity. Remarkably, our model based on macroscopic variables succeeds despite consistent inter-individual differences in neuronal activation. Thus, our analytical framework reconciles consistent individual differences in neuronal activation with macroscopic dynamics that operate universally across individuals. eLife Sciences Publications, Ltd 2019-07-11 /pmc/articles/PMC6624016/ /pubmed/31294689 http://dx.doi.org/10.7554/eLife.46814 Text en © 2019, Brennan and Proekt http://creativecommons.org/licenses/by/4.0/ 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 Computational and Systems Biology
Brennan, Connor
Proekt, Alexander
A quantitative model of conserved macroscopic dynamics predicts future motor commands
title A quantitative model of conserved macroscopic dynamics predicts future motor commands
title_full A quantitative model of conserved macroscopic dynamics predicts future motor commands
title_fullStr A quantitative model of conserved macroscopic dynamics predicts future motor commands
title_full_unstemmed A quantitative model of conserved macroscopic dynamics predicts future motor commands
title_short A quantitative model of conserved macroscopic dynamics predicts future motor commands
title_sort quantitative model of conserved macroscopic dynamics predicts future motor commands
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624016/
https://www.ncbi.nlm.nih.gov/pubmed/31294689
http://dx.doi.org/10.7554/eLife.46814
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