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Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter

Mesostriatal dopaminergic neurons possess extensively branched axonal arbours. Whether action potentials are converted to dopamine output in the striatum will be influenced dynamically and critically by axonal properties and mechanisms that are poorly understood. Here, we address the roles for mecha...

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Autores principales: Condon, Mark D., Platt, Nicola J., Zhang, Yan-Feng, Roberts, Bradley M., Clements, Michael A., Vietti-Michelina, Stefania, Tseu, Min-Yee, Brimblecombe, Katherine R., Threlfell, Sarah, Mann, Edward O., Cragg, Stephanie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753151/
https://www.ncbi.nlm.nih.gov/pubmed/31537790
http://dx.doi.org/10.1038/s41467-019-12264-9
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author Condon, Mark D.
Platt, Nicola J.
Zhang, Yan-Feng
Roberts, Bradley M.
Clements, Michael A.
Vietti-Michelina, Stefania
Tseu, Min-Yee
Brimblecombe, Katherine R.
Threlfell, Sarah
Mann, Edward O.
Cragg, Stephanie J.
author_facet Condon, Mark D.
Platt, Nicola J.
Zhang, Yan-Feng
Roberts, Bradley M.
Clements, Michael A.
Vietti-Michelina, Stefania
Tseu, Min-Yee
Brimblecombe, Katherine R.
Threlfell, Sarah
Mann, Edward O.
Cragg, Stephanie J.
author_sort Condon, Mark D.
collection PubMed
description Mesostriatal dopaminergic neurons possess extensively branched axonal arbours. Whether action potentials are converted to dopamine output in the striatum will be influenced dynamically and critically by axonal properties and mechanisms that are poorly understood. Here, we address the roles for mechanisms governing release probability and axonal activity in determining short‐term plasticity of dopamine release, using fast‐scan cyclic voltammetry in the ex vivo mouse striatum. We show that brief short‐term facilitation and longer short term depression are only weakly dependent on the level of initial release, i.e. are release insensitive. Rather, short-term plasticity is strongly determined by mechanisms which govern axonal activation, including K(+)‐gated excitability and the dopamine transporter, particularly in the dorsal striatum. We identify the dopamine transporter as a master regulator of dopamine short‐term plasticity, governing the balance between release‐dependent and independent mechanisms that also show region‐specific gating.
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spelling pubmed-67531512019-09-23 Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter Condon, Mark D. Platt, Nicola J. Zhang, Yan-Feng Roberts, Bradley M. Clements, Michael A. Vietti-Michelina, Stefania Tseu, Min-Yee Brimblecombe, Katherine R. Threlfell, Sarah Mann, Edward O. Cragg, Stephanie J. Nat Commun Article Mesostriatal dopaminergic neurons possess extensively branched axonal arbours. Whether action potentials are converted to dopamine output in the striatum will be influenced dynamically and critically by axonal properties and mechanisms that are poorly understood. Here, we address the roles for mechanisms governing release probability and axonal activity in determining short‐term plasticity of dopamine release, using fast‐scan cyclic voltammetry in the ex vivo mouse striatum. We show that brief short‐term facilitation and longer short term depression are only weakly dependent on the level of initial release, i.e. are release insensitive. Rather, short-term plasticity is strongly determined by mechanisms which govern axonal activation, including K(+)‐gated excitability and the dopamine transporter, particularly in the dorsal striatum. We identify the dopamine transporter as a master regulator of dopamine short‐term plasticity, governing the balance between release‐dependent and independent mechanisms that also show region‐specific gating. Nature Publishing Group UK 2019-09-19 /pmc/articles/PMC6753151/ /pubmed/31537790 http://dx.doi.org/10.1038/s41467-019-12264-9 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
Condon, Mark D.
Platt, Nicola J.
Zhang, Yan-Feng
Roberts, Bradley M.
Clements, Michael A.
Vietti-Michelina, Stefania
Tseu, Min-Yee
Brimblecombe, Katherine R.
Threlfell, Sarah
Mann, Edward O.
Cragg, Stephanie J.
Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title_full Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title_fullStr Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title_full_unstemmed Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title_short Plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
title_sort plasticity in striatal dopamine release is governed by release-independent depression and the dopamine transporter
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753151/
https://www.ncbi.nlm.nih.gov/pubmed/31537790
http://dx.doi.org/10.1038/s41467-019-12264-9
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