Dopaminergic mechanisms underlying normal variation in trait anxiety: supplemental
Data files
Sep 05, 2018 version files 342.17 KB
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Berry_supplement_striatum_laterality.pdf
Sep 05, 2018 version files 812.70 KB
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Berry_supplemental.docx
Sep 05, 2018 version files 700.47 KB
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Berry_supplemental_02Jan19.pdf
Sep 05, 2018 version files 699.17 KB
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Berry_supplemental_02Jan19.pdf
Abstract
Trait anxiety has been associated with altered activity within corticolimbic pathways connecting the amygdala and rostral anterior cingulate cortex (rACC), which receive rich dopaminergic input. Though the popular culture uses the term “chemical imbalance” to describe the pathophysiology of psychiatric conditions such as anxiety disorders, we know little about how individual differences in human dopamine neurochemistry are related to variation in anxiety and activity within corticolimbic circuits. We addressed this issue by examining inter-individual variability in dopamine release at rest using [11C]raclopride PET, functional connectivity between amygdala and rACC using resting-state fMRI, and trait anxiety measures in healthy adult male and female humans. To measure endogenous dopamine release, we collected two [11C]raclopride PET scans per participant. We contrasted baseline [11C]raclopride D2/3 receptor binding and D2/3 binding following oral methylphenidate administration. Methylphenidate blocks the dopamine transporter, which increases extracellular dopamine and leads to reduced [11C]raclopride D2/3 receptor binding via competitive displacement. We found a negative relationship between dopamine release and trait anxiety such that individuals with higher dopamine release in the amygdala and rACC self-reported lower trait anxiety. Lower trait anxiety was also associated with reduced rACC-amygdala functional connectivity at baseline. Further, functional connectivity showed a modest negative relationship with dopamine release such that reduced rACC-amygdala functional connectivity was accompanied by higher levels of dopamine release in these regions. Together, these findings contribute to hypodopaminergic models of anxiety and support the utility of combining fMRI and PET measures of neurochemical function to advance our understanding of basic affective processes in humans.
Methods
Supplemental materials are provided here, which include analyses of dopamine release in striatum and relationships with trait anxiety. Additionally, we include analysis of right vs left hemisphere dopamine release and funcitonal connectivity for amygdala and rostral anterior cingulate cortex.