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Dopamine signaling in food addiction: role of dopamine D2 receptors

Dopamine (DA) regulates emotional and motivational behavior through the mesolimbic dopaminergic pathway. Changes in DA signaling in mesolimbic neurotransmission are widely believed to modify reward-related behaviors and are therefore closely associated with drug addiction. Recent evidence now sugges...

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Autor principal: Baik, Ja-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133846/
https://www.ncbi.nlm.nih.gov/pubmed/24238362
http://dx.doi.org/10.5483/BMBRep.2013.46.11.207
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author Baik, Ja-Hyun
author_facet Baik, Ja-Hyun
author_sort Baik, Ja-Hyun
collection PubMed
description Dopamine (DA) regulates emotional and motivational behavior through the mesolimbic dopaminergic pathway. Changes in DA signaling in mesolimbic neurotransmission are widely believed to modify reward-related behaviors and are therefore closely associated with drug addiction. Recent evidence now suggests that as with drug addiction, obesity with compulsive eating behaviors involves reward circuitry of the brain, particularly the circuitry involving dopaminergic neural substrates. Increasing amounts of data from human imaging studies, together with genetic analysis, have demonstrated that obese people and drug addicts tend to show altered expression of DA D2 receptors in specific brain areas, and that similar brain areas are activated by food-related and drug-related cues. This review focuses on the functions of the DA system, with specific focus on the physiological interpretation and the role of DA D2 receptor signaling in food addiction. [BMB Reports 2013; 46(11): 519-526]
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spelling pubmed-41338462014-09-16 Dopamine signaling in food addiction: role of dopamine D2 receptors Baik, Ja-Hyun BMB Rep Review Article Dopamine (DA) regulates emotional and motivational behavior through the mesolimbic dopaminergic pathway. Changes in DA signaling in mesolimbic neurotransmission are widely believed to modify reward-related behaviors and are therefore closely associated with drug addiction. Recent evidence now suggests that as with drug addiction, obesity with compulsive eating behaviors involves reward circuitry of the brain, particularly the circuitry involving dopaminergic neural substrates. Increasing amounts of data from human imaging studies, together with genetic analysis, have demonstrated that obese people and drug addicts tend to show altered expression of DA D2 receptors in specific brain areas, and that similar brain areas are activated by food-related and drug-related cues. This review focuses on the functions of the DA system, with specific focus on the physiological interpretation and the role of DA D2 receptor signaling in food addiction. [BMB Reports 2013; 46(11): 519-526] Korean Society for Biochemistry and Molecular Biology 2013-11 /pmc/articles/PMC4133846/ /pubmed/24238362 http://dx.doi.org/10.5483/BMBRep.2013.46.11.207 Text en Copyright © 2013, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Baik, Ja-Hyun
Dopamine signaling in food addiction: role of dopamine D2 receptors
title Dopamine signaling in food addiction: role of dopamine D2 receptors
title_full Dopamine signaling in food addiction: role of dopamine D2 receptors
title_fullStr Dopamine signaling in food addiction: role of dopamine D2 receptors
title_full_unstemmed Dopamine signaling in food addiction: role of dopamine D2 receptors
title_short Dopamine signaling in food addiction: role of dopamine D2 receptors
title_sort dopamine signaling in food addiction: role of dopamine d2 receptors
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133846/
https://www.ncbi.nlm.nih.gov/pubmed/24238362
http://dx.doi.org/10.5483/BMBRep.2013.46.11.207
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