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      Human dopamine receptor D2/D3 availability predicts amygdala reactivity to unpleasant stimuli

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          Abstract

          Dopamine (DA) modulates the response of the amygdala. However, the relation between dopaminergic neurotransmission in striatal and extrastriatal brain regions and amygdala reactivity to affective stimuli has not yet been established. To address this issue, we measured DA D2/D3 receptor (DRD2/3) availability in twenty‐eight healthy men (nicotine‐dependent smokers and never‐smokers) using positron emission tomography with [ 18F]fallypride. In the same group of participants, amygdala response to unpleasant visual stimuli was determined using blood oxygen level‐dependent (BOLD) functional magnetic resonance imaging. The effects of DRD2/3 availability in emotion‐related brain regions and nicotine dependence on amygdala response to unpleasant stimuli were examined by multiple regression analysis. We observed enhanced prefrontal DRD2/3 availability in those individuals with higher amygdala response to unpleasant stimuli. As compared to never‐smokers, smokers showed an attenuated amygdala BOLD response to unpleasant stimuli. Thus, individuals with high prefrontal DRD2/3 availability may be more responsive toward aversive and stressful information. Through this mechanism, dopaminergic neurotransmission might influence vulnerability for affective and anxiety disorders. Neuronal reactivity to unpleasant stimuli seems to be reduced by smoking. This observation could explain increased smoking rates in individuals with mental disorders. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc.

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          Author and article information

          Contributors
          michael.smolka@tu-dresden.de
          Journal
          Hum Brain Mapp
          Hum Brain Mapp
          10.1002/(ISSN)1097-0193
          HBM
          Human Brain Mapping
          Wiley Subscription Services, Inc., A Wiley Company (Hoboken )
          1065-9471
          1097-0193
          10 November 2009
          May 2010
          : 31
          : 5 ( doiID: 10.1002/hbm.v31:5 )
          : 716-726
          Affiliations
          [ 1 ]Department of Addictive Behavior and Addiction Medicine, Central Institute of Mental Health, University of Heidelberg, Mannheim, Germany
          [ 2 ]Department of Psychiatry and Psychotherapy, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
          [ 3 ]Department of Nuclear Medicine, University of Mainz, Mainz, Germany
          [ 4 ]Department of Psychiatry, University of Mainz, Mainz, Germany
          [ 5 ]Department of Psychiatry and Psychotherapy, RWTH Aachen University, Aachen, Germany
          [ 6 ]Department of Nuclear Medicine, Ludwig Maximilian University, Munich, Germany
          Author notes
          [*] [* ]Section of Systems Neuroscience, Department of Psychiatry and Psychotherapy, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Würzburger Str. 35, 01187 Dresden, Germany
          Article
          PMC6870940 PMC6870940 6870940 HBM20900
          10.1002/hbm.20900
          6870940
          19904802
          a7905483-b939-4ffd-91db-ab5a497c3b8e
          Copyright © 2009 Wiley‐Liss, Inc.
          History
          : 02 March 2009
          : 17 July 2009
          : 03 August 2009
          Page count
          Figures: 2, Tables: 1, References: 67, Pages: 11, Words: 0
          Funding
          Funded by: Deutsche Forschungsgemeinschaft (DFG)
          Award ID: SM 80/1‐1
          Award ID: SM 80/1‐2
          Award ID: SM 80/2‐2
          Award ID: SM 80/5‐1
          Funded by: University of Mainz [Mainz‐Forschungsfonds (MAIFOR) program]
          Categories
          Research Article
          Research Articles
          Custom metadata
          2.0
          May 2010
          Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.2 mode:remove_FC converted:15.11.2019

          emotion processing,prefrontal cortex,amygdala,fMRI,PET,[18F]fallypride

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