4.6 Article

Fear Extinction Recall Modulates Human Frontomedial Theta and Amygdala Activity

Journal

CEREBRAL CORTEX
Volume 29, Issue 2, Pages 701-715

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhx353

Keywords

fear conditioning; fear extinction; frontal-midline theta; simultaneous EEG-fMRI; threat processing

Categories

Funding

  1. Deutsche Forschungsgemeinschaft [DFG MU3535/2-3]
  2. Justus Liebig University Giessen (Germany)
  3. PROMOS scholarship of the German Academic Exchange Service (DAAD)
  4. Young Researcher Award of the World Association for Stress Related and Anxiety Disorders (WASAD)
  5. NIH [R37 MH068376, R01 MH096987, 4R00MH094438-03]
  6. DFG [MU3535/2-3, MU3535/2-1]

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Human functional magnetic resonance imaging (fMRI) and electroencephalography (EEG) studies, as well as animal studies, indicate that the amygdala and frontomedial brain regions are critically involved in conditioned fear and that frontomedial oscillations in the theta range (4-8 Hz) may support communication between these brain regions. However, few studies have used a multimodal approach to probe interactions among these key regions in humans. Here, our goal was to bridge the gap between prior human fMRI, EEG, and animal findings. Using simultaneous EEG-fMRI recordings 24 h after fear conditioning and extinction, conditioned stimuli presented (CS+E, CS-E) and not presented during extinction (CS+N, CS-N) were compared to identify effects specific to extinction versus fear recall. Differential (CS+ vs. CS-) electrodermal, frontomedial theta (EEG) and amygdala responses (fMRI) were reduced for extinguished versus nonextinguished stimuli. Importantly, effects on theta power covaried with effects on amygdala activation. Fear and extinction recall as indicated by theta explained 60% of the variance for the analogous effect in the right amygdala. Our findings show for the first time the interplay of amygdala and frontomedial theta activity during fear and extinction recall in humans and provide insight into neural circuits consistently linked with top-down amygdala modulation in rodents.

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