Amygdala damage affects event-related potentials for fearful faces at specific time windows

Pia Rotshtein, Mark P. Richardson, Joel S. Winston, Stefan J. Kiebel, Patrik Vuilleumier, Martin Eimer, Jon Driver, Raymond J. Dolan

Research output: Contribution to journalArticlepeer-review


The amygdala is known to influence processing of threat-related stimuli in distant brain regions, including visual cortex. The time-course of these distant influences is unknown, although this information is important for resolving debates over likely pathways mediating an apparent rapidity in emotional processing. To address this, we recorded event-related potentials (ERPs) to seen fearful face expressions, in preoperative patients with medial temporal lobe epilepsy who had varying degrees of amygdala pathology, plus healthy volunteers. We found that amygdala damage diminished ERPs for fearful versus neutral faces within the P1 time-range, ∼100-150 ms, and for a later component at ∼500-600 ms. Individual severity of amygdala damage determined the magnitude of both these effects, consistent with a causal amygdala role. By contrast, amygdala damage did not affect explicit perception of fearful expressions nor a distinct emotional ERP effect at 150-250 ms. These results demonstrate two distinct time-points at which the amygdala influences fear processing. The data also demonstrate that while not all aspects of expression processing are disrupted by amygdala damage, there is a crucial impact on an early P1 component. These findings are consistent with the existence of multiple processing stages or routes for fearful faces that vary in their dependence on amygdala function.

Original languageEnglish
Pages (from-to)1089-1105
Number of pages17
JournalHuman Brain Mapping
Issue number7
StatePublished - Jul 2010
Externally publishedYes


  • ERP
  • Emotion
  • Late-P3
  • Medial temporal lobe epilepsy
  • P1
  • SPM5

ASJC Scopus subject areas

  • Anatomy
  • Radiological and Ultrasound Technology
  • Radiology Nuclear Medicine and imaging
  • Neurology
  • Clinical Neurology


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