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Dopamine Regulation of Social Choice in a Monogamous Rodent Species

There is growing appreciation that social decision making in humans is strongly influenced by hedonic and emotional processing. The field of social neuroeconomics has shown that neural systems important for reward are associated with social choice and social preferences in humans. Here, we show that...

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Detalles Bibliográficos
Autores principales: Aragona, Brandon J., Wang, Zuoxin
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729670/
https://www.ncbi.nlm.nih.gov/pubmed/19707518
http://dx.doi.org/10.3389/neuro.08.015.2009
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author Aragona, Brandon J.
Wang, Zuoxin
author_facet Aragona, Brandon J.
Wang, Zuoxin
author_sort Aragona, Brandon J.
collection PubMed
description There is growing appreciation that social decision making in humans is strongly influenced by hedonic and emotional processing. The field of social neuroeconomics has shown that neural systems important for reward are associated with social choice and social preferences in humans. Here, we show that the neurobiology of social preferences in a monogamous rodent species, the prairie vole, is also regulated by neural systems involved in reward and emotional processing. Specifically, we describe how mesolimbic dopamine transmission differentially mediates the formation and maintenance of monogamous pair bonds in this species. Thus, reward processing exerts tremendous regulation over social choice behaviors that serve as the foundation of a rather complex social organization. We conclude that prairie voles are an excellent model system for the neuroscience of social choice and that complex social decision-making can be robustly explained by reward and hedonic processing.
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spelling pubmed-27296702009-08-24 Dopamine Regulation of Social Choice in a Monogamous Rodent Species Aragona, Brandon J. Wang, Zuoxin Front Behav Neurosci Neuroscience There is growing appreciation that social decision making in humans is strongly influenced by hedonic and emotional processing. The field of social neuroeconomics has shown that neural systems important for reward are associated with social choice and social preferences in humans. Here, we show that the neurobiology of social preferences in a monogamous rodent species, the prairie vole, is also regulated by neural systems involved in reward and emotional processing. Specifically, we describe how mesolimbic dopamine transmission differentially mediates the formation and maintenance of monogamous pair bonds in this species. Thus, reward processing exerts tremendous regulation over social choice behaviors that serve as the foundation of a rather complex social organization. We conclude that prairie voles are an excellent model system for the neuroscience of social choice and that complex social decision-making can be robustly explained by reward and hedonic processing. Frontiers Research Foundation 2009-08-11 /pmc/articles/PMC2729670/ /pubmed/19707518 http://dx.doi.org/10.3389/neuro.08.015.2009 Text en Copyright © 2009 Aragona and Wang. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Aragona, Brandon J.
Wang, Zuoxin
Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title_full Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title_fullStr Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title_full_unstemmed Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title_short Dopamine Regulation of Social Choice in a Monogamous Rodent Species
title_sort dopamine regulation of social choice in a monogamous rodent species
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729670/
https://www.ncbi.nlm.nih.gov/pubmed/19707518
http://dx.doi.org/10.3389/neuro.08.015.2009
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