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The mixed serotonin receptor agonist psilocybin reduces threat-induced modulation of amygdala connectivity
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4483008
Author(s) Kraehenmann, Rainer; Schmidt, André; Friston, Karl; Preller, Katrin H.; Seifritz, Erich; Vollenweider, Franz X.
Author(s) at UniBasel Schmidt, André
Year 2016
Title The mixed serotonin receptor agonist psilocybin reduces threat-induced modulation of amygdala connectivity
Journal NeuroImage: Clinical
Volume 11
Pages / Article-Number 53-60
Keywords Serotonin; Psilocybin; Depression; fMRI; Dynamic causal modeling
Mesh terms Adult; Amygdala, physiopathology; Bayes Theorem; Brain Mapping; Fear, drug effects; Female; Humans; Male; Neural Pathways, drug effects; Prefrontal Cortex, drug effects; Psilocybin, pharmacology; Serotonin Receptor Agonists, pharmacology; Young Adult
Abstract Stimulation of serotonergic neurotransmission by psilocybin has been shown to shift emotional biases away from negative towards positive stimuli. We have recently shown that reduced amygdala activity during threat processing might underlie psilocybin's effect on emotional processing. However, it is still not known whether psilocybin modulates bottom-up or top-down connectivity within the visual-limbic-prefrontal network underlying threat processing. We therefore analyzed our previous fMRI data using dynamic causal modeling and used Bayesian model selection to infer how psilocybin modulated effective connectivity within the visual-limbic-prefrontal network during threat processing. First, both placebo and psilocybin data were best explained by a model in which threat affect modulated bidirectional connections between the primary visual cortex, amygdala, and lateral prefrontal cortex. Second, psilocybin decreased the threat-induced modulation of top-down connectivity from the amygdala to primary visual cortex, speaking to a neural mechanism that might underlie putative shifts towards positive affect states after psilocybin administration. These findings may have important implications for the treatment of mood and anxiety disorders.
Publisher Elsevier
ISSN/ISBN 2213-1582
edoc-URL https://edoc.unibas.ch/63102/
Full Text on edoc Available
Digital Object Identifier DOI 10.1016/j.nicl.2015.08.009
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/26909323
ISI-Number 000379504500008
Document type (ISI) Journal Article
 
   

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