TY - JOUR
T1 - Effects of acute tryptophan depletion on prefrontal-amygdala connectivity while viewing facial signals of aggression
AU - Passamonti, Luca
AU - Crockett, Molly J.
AU - Apergis-Schoute, Annemieke M.
AU - Clark, Luke
AU - Rowe, James B.
AU - Calder, Andrew J.
AU - Robbins, Trevor W.
N1 - Funding Information:
This study was supported by the James S. McDonnell Foundation 21st Century Collaborative Award/Bridging Brain, Mind and Behavior (Award No. 22002015501 ) to E. A. Phelps and T. W. Robbins and completed within the Behavioural and Clinical Neuroscience Institute, which is cofunded by the Medical Research Council and the Wellcome Trust. Dr. Passamonti was funded by the Betty Behrens Research Fellowship at the Clare Hall College of the University of Cambridge. The J. S. McDonnell Foundation Network grant supported Dr. Apergis-Schoute. Dr. Crockett was supported by the National Science Foundation. Dr. Rowe was supported by the Wellcome Trust (Grant No. WT 088324 ); Dr. Calder by the Medical Research Council (Project Code MC_US_A060_0017 ). Development of the MacBrain Face Stimulus Set (NimStim) was overseen by Nim Tottenham and supported by the John D. and Catherine T. MacArthur Foundation Research Network on Early Experience and Brain Development. Please contact Nim Tottenham at [email protected] for more information concerning the stimulus set.
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Background: Reduced levels of serotonin (5-HT) within prefrontal cortex (PFC)amygdala circuits have long been implicated in impulsive aggression. However, whether lowering 5-HT alters the dynamic interplay between the PFC and the amygdala has not been directly tested in humans. It is known that manipulating 5-HT via acute tryptophan depletion (ATD) causes variable effects on brain responses to a variety of emotional stimuli, but it remains unclear whether ATD affects functional connectivity in neural networks involved in processing social signals of aggression (e.g., angry faces). Methods: Thirty healthy individuals were enrolled in a randomized, double-blind, placebo-controlled ATD study. On each treatment, brain responses to angry, sad, and neutral faces were measured with functional magnetic resonance imaging. Two methods (psycho-physiological-interaction in a general linear model and dynamic causal modeling) were used to assess the impact of ATD on the functional connectivity between PFC and amygdala. Results: Data from 19 subjects were available for the final analyses. A whole-brain psycho-physiological-interaction in a general linear model showed that ATD significantly modulated the connectivity between the amygdala and two PFC regions (ventral anterior cingulate cortex and ventrolateral PFC) when processing angry vs. neutral and angry vs. sad but not sad vs. neutral faces. Dynamic causal modeling corroborated and extended these findings by showing that 5-HT depletion reduced the influence of processing angry vs. neutral faces on circuits within PFC and on PFCamygdala pathways. Conclusions: We provide strong support for neurobiological accounts positing that 5-HT significantly influences PFCamygdala circuits implicated in aggression and other affective behaviors.
AB - Background: Reduced levels of serotonin (5-HT) within prefrontal cortex (PFC)amygdala circuits have long been implicated in impulsive aggression. However, whether lowering 5-HT alters the dynamic interplay between the PFC and the amygdala has not been directly tested in humans. It is known that manipulating 5-HT via acute tryptophan depletion (ATD) causes variable effects on brain responses to a variety of emotional stimuli, but it remains unclear whether ATD affects functional connectivity in neural networks involved in processing social signals of aggression (e.g., angry faces). Methods: Thirty healthy individuals were enrolled in a randomized, double-blind, placebo-controlled ATD study. On each treatment, brain responses to angry, sad, and neutral faces were measured with functional magnetic resonance imaging. Two methods (psycho-physiological-interaction in a general linear model and dynamic causal modeling) were used to assess the impact of ATD on the functional connectivity between PFC and amygdala. Results: Data from 19 subjects were available for the final analyses. A whole-brain psycho-physiological-interaction in a general linear model showed that ATD significantly modulated the connectivity between the amygdala and two PFC regions (ventral anterior cingulate cortex and ventrolateral PFC) when processing angry vs. neutral and angry vs. sad but not sad vs. neutral faces. Dynamic causal modeling corroborated and extended these findings by showing that 5-HT depletion reduced the influence of processing angry vs. neutral faces on circuits within PFC and on PFCamygdala pathways. Conclusions: We provide strong support for neurobiological accounts positing that 5-HT significantly influences PFCamygdala circuits implicated in aggression and other affective behaviors.
KW - 5-HT
KW - amygdala
KW - anterior cingulate cortex
KW - effective connectivity
KW - fMRI
KW - violence.
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U2 - 10.1016/j.biopsych.2011.07.033
DO - 10.1016/j.biopsych.2011.07.033
M3 - Article
C2 - 21920502
AN - SCOPUS:82755189457
SN - 0006-3223
VL - 71
SP - 36
EP - 43
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 1
ER -