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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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