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Time-dependent assessment of stimulus-evoked regional dopamine release
To date, the spatiotemporal release of specific neurotransmitters at physiological levels in the human brain cannot be detected. Here, we present a method that relates minute-by-minute fluctuations of the positron emission tomography (PET) radioligand [11C]raclopride directly to subsecond dopamine r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338792/ https://www.ncbi.nlm.nih.gov/pubmed/30659189 http://dx.doi.org/10.1038/s41467-018-08143-4 |
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author | Lippert, Rachel N. Cremer, Anna Lena Edwin Thanarajah, Sharmili Korn, Clio Jahans-Price, Thomas Burgeno, Lauren M. Tittgemeyer, Marc Brüning, Jens C. Walton, Mark E. Backes, Heiko |
author_facet | Lippert, Rachel N. Cremer, Anna Lena Edwin Thanarajah, Sharmili Korn, Clio Jahans-Price, Thomas Burgeno, Lauren M. Tittgemeyer, Marc Brüning, Jens C. Walton, Mark E. Backes, Heiko |
author_sort | Lippert, Rachel N. |
collection | PubMed |
description | To date, the spatiotemporal release of specific neurotransmitters at physiological levels in the human brain cannot be detected. Here, we present a method that relates minute-by-minute fluctuations of the positron emission tomography (PET) radioligand [11C]raclopride directly to subsecond dopamine release events. We show theoretically that synaptic dopamine release induces low frequency temporal variations of extrasynaptic extracellular dopamine levels, at time scales of one minute, that can evoke detectable temporal variations in the [11C]raclopride signal. Hence, dopaminergic activity can be monitored via temporal fluctuations in the [11C]raclopride PET signal. We validate this theory using fast-scan cyclic voltammetry and [11C]raclopride PET in mice during chemogenetic activation of dopaminergic neurons. We then apply the method to data from human subjects given a palatable milkshake and discover immediate and—for the first time—delayed food-induced dopamine release. This method enables time-dependent regional monitoring of stimulus-evoked dopamine release at physiological levels. |
format | Online Article Text |
id | pubmed-6338792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63387922019-01-22 Time-dependent assessment of stimulus-evoked regional dopamine release Lippert, Rachel N. Cremer, Anna Lena Edwin Thanarajah, Sharmili Korn, Clio Jahans-Price, Thomas Burgeno, Lauren M. Tittgemeyer, Marc Brüning, Jens C. Walton, Mark E. Backes, Heiko Nat Commun Article To date, the spatiotemporal release of specific neurotransmitters at physiological levels in the human brain cannot be detected. Here, we present a method that relates minute-by-minute fluctuations of the positron emission tomography (PET) radioligand [11C]raclopride directly to subsecond dopamine release events. We show theoretically that synaptic dopamine release induces low frequency temporal variations of extrasynaptic extracellular dopamine levels, at time scales of one minute, that can evoke detectable temporal variations in the [11C]raclopride signal. Hence, dopaminergic activity can be monitored via temporal fluctuations in the [11C]raclopride PET signal. We validate this theory using fast-scan cyclic voltammetry and [11C]raclopride PET in mice during chemogenetic activation of dopaminergic neurons. We then apply the method to data from human subjects given a palatable milkshake and discover immediate and—for the first time—delayed food-induced dopamine release. This method enables time-dependent regional monitoring of stimulus-evoked dopamine release at physiological levels. Nature Publishing Group UK 2019-01-18 /pmc/articles/PMC6338792/ /pubmed/30659189 http://dx.doi.org/10.1038/s41467-018-08143-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lippert, Rachel N. Cremer, Anna Lena Edwin Thanarajah, Sharmili Korn, Clio Jahans-Price, Thomas Burgeno, Lauren M. Tittgemeyer, Marc Brüning, Jens C. Walton, Mark E. Backes, Heiko Time-dependent assessment of stimulus-evoked regional dopamine release |
title | Time-dependent assessment of stimulus-evoked regional dopamine release |
title_full | Time-dependent assessment of stimulus-evoked regional dopamine release |
title_fullStr | Time-dependent assessment of stimulus-evoked regional dopamine release |
title_full_unstemmed | Time-dependent assessment of stimulus-evoked regional dopamine release |
title_short | Time-dependent assessment of stimulus-evoked regional dopamine release |
title_sort | time-dependent assessment of stimulus-evoked regional dopamine release |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338792/ https://www.ncbi.nlm.nih.gov/pubmed/30659189 http://dx.doi.org/10.1038/s41467-018-08143-4 |
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