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Rostral and dorsal anterior cingulate cortex make dissociable contributions during antisaccade error commission.

The anterior cingulate cortex (ACC) participates in both performance optimization and evaluation, with dissociable contributions from dorsal (dACC) and rostral (rACC) regions. Deactivation in rACC and other default-mode regions is important for performance optimization, whereas increased rACC and dACC activation contributes to performance evaluation. Errors activate both rACC and dACC. We propose that this activation reflects differential error-related involvement of rACC and dACC during both performance optimization and evaluation, and that these two processes can be distinguished by the timing of their occurrence within a trial. We compared correct and error antisaccade trials. We expected errors to correlate with an early failure of rACC deactivation and increased activation of both rACC and dACC later in the trial. Eighteen healthy subjects performed a series of prosaccade and antisaccade trials during event-related functional MRI. We estimated the hemodynamic responses for error and correct antisaccades using a finite impulse-response model. We examined ACC activity by comparing error and correct antisaccades with a fixation baseline and error to correct antisaccades directly. Compared with correct antisaccades, errors were characterized by an early bilateral failure of deactivation of rACC and other default-mode regions. This difference was significant in rACC. Errors also were associated with increased activity in both rACC and dACC later in the trial. These results show that accurate performance involves deactivation of the rACC and other default mode regions and suggest that both rACC and dACC contribute to the evaluation of error responses.

Pubmed ID: 16227444 RIS Download

Mesh terms: Adult | Female | Gyrus Cinguli | Humans | Magnetic Resonance Imaging | Male | Middle Aged | Psychomotor Performance | Regression Analysis | Saccades

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Associated grants

  • Agency: NIMH NIH HHS, Id: F31 MH 72120
  • Agency: NINDS NIH HHS, Id: K08 NS 01920
  • Agency: NIMH NIH HHS, Id: R01 MH 67720

SumsDB (Data, Activation Foci)

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