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A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors
Assessing brain activity during complex voluntary motor behaviors that require the recruitment of multiple neural sites is a field of active research. Our current knowledge is primarily based on human brain imaging studies that have clear limitations in terms of temporal and spatial resolution. We d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230744/ https://www.ncbi.nlm.nih.gov/pubmed/25393005 http://dx.doi.org/10.1371/journal.pcbi.1003924 |
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author | Fürtinger, Stefan Zinn, Joel C. Simonyan, Kristina |
author_facet | Fürtinger, Stefan Zinn, Joel C. Simonyan, Kristina |
author_sort | Fürtinger, Stefan |
collection | PubMed |
description | Assessing brain activity during complex voluntary motor behaviors that require the recruitment of multiple neural sites is a field of active research. Our current knowledge is primarily based on human brain imaging studies that have clear limitations in terms of temporal and spatial resolution. We developed a physiologically informed non-linear multi-compartment stochastic neural model to simulate functional brain activity coupled with neurotransmitter release during complex voluntary behavior, such as speech production. Due to its state-dependent modulation of neural firing, dopaminergic neurotransmission plays a key role in the organization of functional brain circuits controlling speech and language and thus has been incorporated in our neural population model. A rigorous mathematical proof establishing existence and uniqueness of solutions to the proposed model as well as a computationally efficient strategy to numerically approximate these solutions are presented. Simulated brain activity during the resting state and sentence production was analyzed using functional network connectivity, and graph theoretical techniques were employed to highlight differences between the two conditions. We demonstrate that our model successfully reproduces characteristic changes seen in empirical data between the resting state and speech production, and dopaminergic neurotransmission evokes pronounced changes in modeled functional connectivity by acting on the underlying biological stochastic neural model. Specifically, model and data networks in both speech and rest conditions share task-specific network features: both the simulated and empirical functional connectivity networks show an increase in nodal influence and segregation in speech over the resting state. These commonalities confirm that dopamine is a key neuromodulator of the functional connectome of speech control. Based on reproducible characteristic aspects of empirical data, we suggest a number of extensions of the proposed methodology building upon the current model. |
format | Online Article Text |
id | pubmed-4230744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42307442014-11-18 A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors Fürtinger, Stefan Zinn, Joel C. Simonyan, Kristina PLoS Comput Biol Research Article Assessing brain activity during complex voluntary motor behaviors that require the recruitment of multiple neural sites is a field of active research. Our current knowledge is primarily based on human brain imaging studies that have clear limitations in terms of temporal and spatial resolution. We developed a physiologically informed non-linear multi-compartment stochastic neural model to simulate functional brain activity coupled with neurotransmitter release during complex voluntary behavior, such as speech production. Due to its state-dependent modulation of neural firing, dopaminergic neurotransmission plays a key role in the organization of functional brain circuits controlling speech and language and thus has been incorporated in our neural population model. A rigorous mathematical proof establishing existence and uniqueness of solutions to the proposed model as well as a computationally efficient strategy to numerically approximate these solutions are presented. Simulated brain activity during the resting state and sentence production was analyzed using functional network connectivity, and graph theoretical techniques were employed to highlight differences between the two conditions. We demonstrate that our model successfully reproduces characteristic changes seen in empirical data between the resting state and speech production, and dopaminergic neurotransmission evokes pronounced changes in modeled functional connectivity by acting on the underlying biological stochastic neural model. Specifically, model and data networks in both speech and rest conditions share task-specific network features: both the simulated and empirical functional connectivity networks show an increase in nodal influence and segregation in speech over the resting state. These commonalities confirm that dopamine is a key neuromodulator of the functional connectome of speech control. Based on reproducible characteristic aspects of empirical data, we suggest a number of extensions of the proposed methodology building upon the current model. Public Library of Science 2014-11-13 /pmc/articles/PMC4230744/ /pubmed/25393005 http://dx.doi.org/10.1371/journal.pcbi.1003924 Text en © 2014 Fuertinger et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Fürtinger, Stefan Zinn, Joel C. Simonyan, Kristina A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title | A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title_full | A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title_fullStr | A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title_full_unstemmed | A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title_short | A Neural Population Model Incorporating Dopaminergic Neurotransmission during Complex Voluntary Behaviors |
title_sort | neural population model incorporating dopaminergic neurotransmission during complex voluntary behaviors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230744/ https://www.ncbi.nlm.nih.gov/pubmed/25393005 http://dx.doi.org/10.1371/journal.pcbi.1003924 |
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