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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6624016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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