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Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation

Motivation to work for potential rewards is critically dependent on dopamine (DA) in the nucleus accumbens (NAc). DA release from NAc axons can be controlled by at least two distinct mechanisms: (1) action potentials propagating from DA cell bodies in the ventral tegmental area (VTA), and (2) activa...

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Autores principales: Mohebi, Ali, Collins, Val L, Berke, Joshua D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259987/
https://www.ncbi.nlm.nih.gov/pubmed/37272423
http://dx.doi.org/10.7554/eLife.85011
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author Mohebi, Ali
Collins, Val L
Berke, Joshua D
author_facet Mohebi, Ali
Collins, Val L
Berke, Joshua D
author_sort Mohebi, Ali
collection PubMed
description Motivation to work for potential rewards is critically dependent on dopamine (DA) in the nucleus accumbens (NAc). DA release from NAc axons can be controlled by at least two distinct mechanisms: (1) action potentials propagating from DA cell bodies in the ventral tegmental area (VTA), and (2) activation of β2* nicotinic receptors by local cholinergic interneurons (CINs). How CIN activity contributes to NAc DA dynamics in behaving animals is not well understood. We monitored DA release in the NAc Core of awake, unrestrained rats using the DA sensor RdLight1, while simultaneously monitoring or manipulating CIN activity at the same location. CIN stimulation rapidly evoked DA release, and in contrast to slice preparations, this DA release showed no indication of short-term depression or receptor desensitization. The sound of unexpected food delivery evoked a brief joint increase in CIN population activity and DA release, with a second joint increase as rats approached the food. In an operant task, we observed fast ramps in CIN activity during approach behaviors, either to start the trial or to collect rewards. These CIN ramps co-occurred with DA release ramps, without corresponding changes in the firing of lateral VTA DA neurons. Finally, we examined the effects of blocking CIN influence over DA release through local NAc infusion of DHβE, a selective antagonist of β2* nicotinic receptors. DHβE dose-dependently interfered with motivated approach decisions, mimicking the effects of a DA antagonist. Our results support a key influence of CINs over motivated behavior via the local regulation of DA release.
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spelling pubmed-102599872023-06-13 Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation Mohebi, Ali Collins, Val L Berke, Joshua D eLife Neuroscience Motivation to work for potential rewards is critically dependent on dopamine (DA) in the nucleus accumbens (NAc). DA release from NAc axons can be controlled by at least two distinct mechanisms: (1) action potentials propagating from DA cell bodies in the ventral tegmental area (VTA), and (2) activation of β2* nicotinic receptors by local cholinergic interneurons (CINs). How CIN activity contributes to NAc DA dynamics in behaving animals is not well understood. We monitored DA release in the NAc Core of awake, unrestrained rats using the DA sensor RdLight1, while simultaneously monitoring or manipulating CIN activity at the same location. CIN stimulation rapidly evoked DA release, and in contrast to slice preparations, this DA release showed no indication of short-term depression or receptor desensitization. The sound of unexpected food delivery evoked a brief joint increase in CIN population activity and DA release, with a second joint increase as rats approached the food. In an operant task, we observed fast ramps in CIN activity during approach behaviors, either to start the trial or to collect rewards. These CIN ramps co-occurred with DA release ramps, without corresponding changes in the firing of lateral VTA DA neurons. Finally, we examined the effects of blocking CIN influence over DA release through local NAc infusion of DHβE, a selective antagonist of β2* nicotinic receptors. DHβE dose-dependently interfered with motivated approach decisions, mimicking the effects of a DA antagonist. Our results support a key influence of CINs over motivated behavior via the local regulation of DA release. eLife Sciences Publications, Ltd 2023-06-05 /pmc/articles/PMC10259987/ /pubmed/37272423 http://dx.doi.org/10.7554/eLife.85011 Text en © 2023, Mohebi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Mohebi, Ali
Collins, Val L
Berke, Joshua D
Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title_full Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title_fullStr Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title_full_unstemmed Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title_short Accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
title_sort accumbens cholinergic interneurons dynamically promote dopamine release and enable motivation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259987/
https://www.ncbi.nlm.nih.gov/pubmed/37272423
http://dx.doi.org/10.7554/eLife.85011
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