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Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.

The shell of the nucleus accumbens (NAcSh) and ventral pallidum (VP) are critical for reward processing, although how coordinated activity within these nuclei orchestrates reward valuation and consumption remains unclear. Inhibition of NAcSh firing is necessary for reward consumption, but the source...

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Autores principales: Vachez, Yvan M., Tooley, Jessica R., Abiraman, Kavitha, Matikainen-Ankney, Bridget, Casey, Eric, Earnest, Tom, Ramos, Leana M., Silberberg, Hanna, Godynyuk, Elizabeth, Uddin, Olivia, Marconi, Lauren, Le Pichon, Claire E., Creed, Meaghan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933121/
https://www.ncbi.nlm.nih.gov/pubmed/33495635
http://dx.doi.org/10.1038/s41593-020-00772-7
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author Vachez, Yvan M.
Tooley, Jessica R.
Abiraman, Kavitha
Matikainen-Ankney, Bridget
Casey, Eric
Earnest, Tom
Ramos, Leana M.
Silberberg, Hanna
Godynyuk, Elizabeth
Uddin, Olivia
Marconi, Lauren
Le Pichon, Claire E.
Creed, Meaghan C.
author_facet Vachez, Yvan M.
Tooley, Jessica R.
Abiraman, Kavitha
Matikainen-Ankney, Bridget
Casey, Eric
Earnest, Tom
Ramos, Leana M.
Silberberg, Hanna
Godynyuk, Elizabeth
Uddin, Olivia
Marconi, Lauren
Le Pichon, Claire E.
Creed, Meaghan C.
author_sort Vachez, Yvan M.
collection PubMed
description The shell of the nucleus accumbens (NAcSh) and ventral pallidum (VP) are critical for reward processing, although how coordinated activity within these nuclei orchestrates reward valuation and consumption remains unclear. Inhibition of NAcSh firing is necessary for reward consumption, but the source of this inhibition remains unknown. Here, we report that a subpopulation of VP neurons, the ventral arkypallidal (vArky) neurons, project back to the NAcSh, where they inhibit NAcSh neurons in vivo in mice. Consistent with this pathway driving reward consumption via inhibition of the NAcSh, calcium activity of vArky neurons scaled with reward palatability and predicted the subsequent drinking behavior during a free-access paradigm, which was dissociable from reward seeking. Activation of the VP to NAchSh pathway increased on-going reward consumption while amplifying hedonic reactions to reward. Our results establish a pivotal role of vArky neurons in promoting reward consumption, through modulating NAcSh firing in a value-dependent manner.
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spelling pubmed-79331212021-07-25 Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption. Vachez, Yvan M. Tooley, Jessica R. Abiraman, Kavitha Matikainen-Ankney, Bridget Casey, Eric Earnest, Tom Ramos, Leana M. Silberberg, Hanna Godynyuk, Elizabeth Uddin, Olivia Marconi, Lauren Le Pichon, Claire E. Creed, Meaghan C. Nat Neurosci Article The shell of the nucleus accumbens (NAcSh) and ventral pallidum (VP) are critical for reward processing, although how coordinated activity within these nuclei orchestrates reward valuation and consumption remains unclear. Inhibition of NAcSh firing is necessary for reward consumption, but the source of this inhibition remains unknown. Here, we report that a subpopulation of VP neurons, the ventral arkypallidal (vArky) neurons, project back to the NAcSh, where they inhibit NAcSh neurons in vivo in mice. Consistent with this pathway driving reward consumption via inhibition of the NAcSh, calcium activity of vArky neurons scaled with reward palatability and predicted the subsequent drinking behavior during a free-access paradigm, which was dissociable from reward seeking. Activation of the VP to NAchSh pathway increased on-going reward consumption while amplifying hedonic reactions to reward. Our results establish a pivotal role of vArky neurons in promoting reward consumption, through modulating NAcSh firing in a value-dependent manner. 2021-01-25 2021-03 /pmc/articles/PMC7933121/ /pubmed/33495635 http://dx.doi.org/10.1038/s41593-020-00772-7 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Vachez, Yvan M.
Tooley, Jessica R.
Abiraman, Kavitha
Matikainen-Ankney, Bridget
Casey, Eric
Earnest, Tom
Ramos, Leana M.
Silberberg, Hanna
Godynyuk, Elizabeth
Uddin, Olivia
Marconi, Lauren
Le Pichon, Claire E.
Creed, Meaghan C.
Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title_full Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title_fullStr Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title_full_unstemmed Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title_short Ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
title_sort ventral arkypallidal neurons inhibit accumbal firing to promote reward consumption.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933121/
https://www.ncbi.nlm.nih.gov/pubmed/33495635
http://dx.doi.org/10.1038/s41593-020-00772-7
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