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Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission
Computational modeling of dopamine transmission is challenged by complex underlying mechanisms. Here we present a new computational model that (I) simultaneously regards release, diffusion and uptake of dopamine, (II) considers multiple terminal release events and (III) comprises both synaptic and v...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728201/ https://www.ncbi.nlm.nih.gov/pubmed/33253315 http://dx.doi.org/10.1371/journal.pcbi.1008410 |
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author | Wiencke, Kathleen Horstmann, Annette Mathar, David Villringer, Arno Neumann, Jane |
author_facet | Wiencke, Kathleen Horstmann, Annette Mathar, David Villringer, Arno Neumann, Jane |
author_sort | Wiencke, Kathleen |
collection | PubMed |
description | Computational modeling of dopamine transmission is challenged by complex underlying mechanisms. Here we present a new computational model that (I) simultaneously regards release, diffusion and uptake of dopamine, (II) considers multiple terminal release events and (III) comprises both synaptic and volume transmission by incorporating the geometry of the synaptic cleft. We were able to validate our model in that it simulates concentration values comparable to physiological values observed in empirical studies. Further, although synaptic dopamine diffuses into extra-synaptic space, our model reflects a very localized signal occurring on the synaptic level, i.e. synaptic dopamine release is negligibly recognized by neighboring synapses. Moreover, increasing evidence suggests that cognitive performance can be predicted by signal variability of neuroimaging data (e.g. BOLD). Signal variability in target areas of dopaminergic neurons (striatum, cortex) may arise from dopamine concentration variability. On that account we compared spatio-temporal variability in a simulation mimicking normal dopamine transmission in striatum to scenarios of enhanced dopamine release and dopamine uptake inhibition. We found different variability characteristics between the three settings, which may in part account for differences in empirical observations. From a clinical perspective, differences in striatal dopaminergic signaling contribute to differential learning and reward processing, with relevant implications for addictive- and compulsive-like behavior. Specifically, dopaminergic tone is assumed to impact on phasic dopamine and hence on the integration of reward-related signals. However, in humans DA tone is classically assessed using PET, which is an indirect measure of endogenous DA availability and suffers from temporal and spatial resolution issues. We discuss how this can lead to discrepancies with observations from other methods such as microdialysis and show how computational modeling can help to refine our understanding of DA transmission. |
format | Online Article Text |
id | pubmed-7728201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77282012020-12-16 Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission Wiencke, Kathleen Horstmann, Annette Mathar, David Villringer, Arno Neumann, Jane PLoS Comput Biol Research Article Computational modeling of dopamine transmission is challenged by complex underlying mechanisms. Here we present a new computational model that (I) simultaneously regards release, diffusion and uptake of dopamine, (II) considers multiple terminal release events and (III) comprises both synaptic and volume transmission by incorporating the geometry of the synaptic cleft. We were able to validate our model in that it simulates concentration values comparable to physiological values observed in empirical studies. Further, although synaptic dopamine diffuses into extra-synaptic space, our model reflects a very localized signal occurring on the synaptic level, i.e. synaptic dopamine release is negligibly recognized by neighboring synapses. Moreover, increasing evidence suggests that cognitive performance can be predicted by signal variability of neuroimaging data (e.g. BOLD). Signal variability in target areas of dopaminergic neurons (striatum, cortex) may arise from dopamine concentration variability. On that account we compared spatio-temporal variability in a simulation mimicking normal dopamine transmission in striatum to scenarios of enhanced dopamine release and dopamine uptake inhibition. We found different variability characteristics between the three settings, which may in part account for differences in empirical observations. From a clinical perspective, differences in striatal dopaminergic signaling contribute to differential learning and reward processing, with relevant implications for addictive- and compulsive-like behavior. Specifically, dopaminergic tone is assumed to impact on phasic dopamine and hence on the integration of reward-related signals. However, in humans DA tone is classically assessed using PET, which is an indirect measure of endogenous DA availability and suffers from temporal and spatial resolution issues. We discuss how this can lead to discrepancies with observations from other methods such as microdialysis and show how computational modeling can help to refine our understanding of DA transmission. Public Library of Science 2020-11-30 /pmc/articles/PMC7728201/ /pubmed/33253315 http://dx.doi.org/10.1371/journal.pcbi.1008410 Text en © 2020 Wiencke 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wiencke, Kathleen Horstmann, Annette Mathar, David Villringer, Arno Neumann, Jane Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title | Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title_full | Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title_fullStr | Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title_full_unstemmed | Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title_short | Dopamine release, diffusion and uptake: A computational model for synaptic and volume transmission |
title_sort | dopamine release, diffusion and uptake: a computational model for synaptic and volume transmission |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728201/ https://www.ncbi.nlm.nih.gov/pubmed/33253315 http://dx.doi.org/10.1371/journal.pcbi.1008410 |
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