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Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward

Insulin activates insulin receptors (InsRs) in the hypothalamus to signal satiety after a meal. However, the rising incidence of obesity, which results in chronically elevated insulin levels, implies that insulin may also act in brain centres that regulate motivation and reward. We report here that...

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Autores principales: Stouffer, Melissa A., Woods, Catherine A., Patel, Jyoti C., Lee, Christian R., Witkovsky, Paul, Bao, Li, Machold, Robert P., Jones, Kymry T., de Vaca, Soledad Cabeza, Reith, Maarten E. A., Carr, Kenneth D., Rice, Margaret E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624275/
https://www.ncbi.nlm.nih.gov/pubmed/26503322
http://dx.doi.org/10.1038/ncomms9543
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author Stouffer, Melissa A.
Woods, Catherine A.
Patel, Jyoti C.
Lee, Christian R.
Witkovsky, Paul
Bao, Li
Machold, Robert P.
Jones, Kymry T.
de Vaca, Soledad Cabeza
Reith, Maarten E. A.
Carr, Kenneth D.
Rice, Margaret E.
author_facet Stouffer, Melissa A.
Woods, Catherine A.
Patel, Jyoti C.
Lee, Christian R.
Witkovsky, Paul
Bao, Li
Machold, Robert P.
Jones, Kymry T.
de Vaca, Soledad Cabeza
Reith, Maarten E. A.
Carr, Kenneth D.
Rice, Margaret E.
author_sort Stouffer, Melissa A.
collection PubMed
description Insulin activates insulin receptors (InsRs) in the hypothalamus to signal satiety after a meal. However, the rising incidence of obesity, which results in chronically elevated insulin levels, implies that insulin may also act in brain centres that regulate motivation and reward. We report here that insulin can amplify action potential-dependent dopamine (DA) release in the nucleus accumbens (NAc) and caudate–putamen through an indirect mechanism that involves striatal cholinergic interneurons that express InsRs. Furthermore, two different chronic diet manipulations in rats, food restriction (FR) and an obesogenic (OB) diet, oppositely alter the sensitivity of striatal DA release to insulin, with enhanced responsiveness in FR, but loss of responsiveness in OB. Behavioural studies show that intact insulin levels in the NAc shell are necessary for acquisition of preference for the flavour of a paired glucose solution. Together, these data imply that striatal insulin signalling enhances DA release to influence food choices.
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spelling pubmed-46242752015-12-08 Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward Stouffer, Melissa A. Woods, Catherine A. Patel, Jyoti C. Lee, Christian R. Witkovsky, Paul Bao, Li Machold, Robert P. Jones, Kymry T. de Vaca, Soledad Cabeza Reith, Maarten E. A. Carr, Kenneth D. Rice, Margaret E. Nat Commun Article Insulin activates insulin receptors (InsRs) in the hypothalamus to signal satiety after a meal. However, the rising incidence of obesity, which results in chronically elevated insulin levels, implies that insulin may also act in brain centres that regulate motivation and reward. We report here that insulin can amplify action potential-dependent dopamine (DA) release in the nucleus accumbens (NAc) and caudate–putamen through an indirect mechanism that involves striatal cholinergic interneurons that express InsRs. Furthermore, two different chronic diet manipulations in rats, food restriction (FR) and an obesogenic (OB) diet, oppositely alter the sensitivity of striatal DA release to insulin, with enhanced responsiveness in FR, but loss of responsiveness in OB. Behavioural studies show that intact insulin levels in the NAc shell are necessary for acquisition of preference for the flavour of a paired glucose solution. Together, these data imply that striatal insulin signalling enhances DA release to influence food choices. Nature Pub. Group 2015-10-27 /pmc/articles/PMC4624275/ /pubmed/26503322 http://dx.doi.org/10.1038/ncomms9543 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Stouffer, Melissa A.
Woods, Catherine A.
Patel, Jyoti C.
Lee, Christian R.
Witkovsky, Paul
Bao, Li
Machold, Robert P.
Jones, Kymry T.
de Vaca, Soledad Cabeza
Reith, Maarten E. A.
Carr, Kenneth D.
Rice, Margaret E.
Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title_full Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title_fullStr Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title_full_unstemmed Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title_short Insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
title_sort insulin enhances striatal dopamine release by activating cholinergic interneurons and thereby signals reward
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624275/
https://www.ncbi.nlm.nih.gov/pubmed/26503322
http://dx.doi.org/10.1038/ncomms9543
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