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Mesolimbic dopamine D2 receptors and neural representations of subjective value
The process by which the value of delayed rewards is discounted varies from person to person. It has been suggested that these individual differences in subjective valuation of delayed rewards are supported by mesolimbic dopamine D2-like receptors (D2Rs) in the ventral striatum. However, no study to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934551/ https://www.ncbi.nlm.nih.gov/pubmed/31882947 http://dx.doi.org/10.1038/s41598-019-56858-1 |
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author | Castrellon, Jaime J. Young, Jacob S. Dang, Linh C. Cowan, Ronald L. Zald, David H. Samanez-Larkin, Gregory R. |
author_facet | Castrellon, Jaime J. Young, Jacob S. Dang, Linh C. Cowan, Ronald L. Zald, David H. Samanez-Larkin, Gregory R. |
author_sort | Castrellon, Jaime J. |
collection | PubMed |
description | The process by which the value of delayed rewards is discounted varies from person to person. It has been suggested that these individual differences in subjective valuation of delayed rewards are supported by mesolimbic dopamine D2-like receptors (D2Rs) in the ventral striatum. However, no study to date has documented an association between direct measures of dopamine receptors and neural representations of subjective value in humans. Here, we examined whether individual differences in D2R availability were related to neural subjective value signals during decision making. Human participants completed a monetary delay discounting task during an fMRI scan and on a separate visit completed a PET scan with the high affinity D2R tracer [18 F]fallypride. Region-of-interest analyses revealed that D2R availability in the ventral striatum was positively correlated with subjective value-related activity in the ventromedial prefrontal cortex and midbrain but not with choice behavior. Whole-brain analyses revealed a positive correlation between ventral striatum D2R availability and subjective value-related activity in the left inferior frontal gyrus and superior insula. These findings identify a link between a direct measure of mesolimbic dopamine function and subjective value representation in humans and suggest a mechanism by which individuals vary in neural representation of discounted subjective value. |
format | Online Article Text |
id | pubmed-6934551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69345512019-12-29 Mesolimbic dopamine D2 receptors and neural representations of subjective value Castrellon, Jaime J. Young, Jacob S. Dang, Linh C. Cowan, Ronald L. Zald, David H. Samanez-Larkin, Gregory R. Sci Rep Article The process by which the value of delayed rewards is discounted varies from person to person. It has been suggested that these individual differences in subjective valuation of delayed rewards are supported by mesolimbic dopamine D2-like receptors (D2Rs) in the ventral striatum. However, no study to date has documented an association between direct measures of dopamine receptors and neural representations of subjective value in humans. Here, we examined whether individual differences in D2R availability were related to neural subjective value signals during decision making. Human participants completed a monetary delay discounting task during an fMRI scan and on a separate visit completed a PET scan with the high affinity D2R tracer [18 F]fallypride. Region-of-interest analyses revealed that D2R availability in the ventral striatum was positively correlated with subjective value-related activity in the ventromedial prefrontal cortex and midbrain but not with choice behavior. Whole-brain analyses revealed a positive correlation between ventral striatum D2R availability and subjective value-related activity in the left inferior frontal gyrus and superior insula. These findings identify a link between a direct measure of mesolimbic dopamine function and subjective value representation in humans and suggest a mechanism by which individuals vary in neural representation of discounted subjective value. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934551/ /pubmed/31882947 http://dx.doi.org/10.1038/s41598-019-56858-1 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 Castrellon, Jaime J. Young, Jacob S. Dang, Linh C. Cowan, Ronald L. Zald, David H. Samanez-Larkin, Gregory R. Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title | Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title_full | Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title_fullStr | Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title_full_unstemmed | Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title_short | Mesolimbic dopamine D2 receptors and neural representations of subjective value |
title_sort | mesolimbic dopamine d2 receptors and neural representations of subjective value |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934551/ https://www.ncbi.nlm.nih.gov/pubmed/31882947 http://dx.doi.org/10.1038/s41598-019-56858-1 |
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