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Human Dorsal Anterior Cingulate Cortex Neurons Mediate Ongoing Behavioral Adaptation
  • Published Date:
    Aug 9 2012
  • Source:
    Nature. 488(7410):218-221.
Filetype[PDF-655.99 KB]


Details:
  • Pubmed ID:
    22722841
  • Pubmed Central ID:
    PMC3416924
  • Description:
    The ability to optimize behavioural performance when confronted with continuously evolving environmental demands is a key element of human cognition. The dorsal anterior cingulate cortex (dACC), which lies on the medial surface of the frontal lobes, is important in regulating cognitive control. Hypotheses about its function include guiding reward-based decision making, monitoring for conflict between competing responses and predicting task difficulty. Precise mechanisms of dACC function remain unknown, however, because of the limited number of human neurophysiological studies. Here we use functional imaging and human single-neuron recordings to show that the firing of individual dACC neurons encodes current and recent cognitive load. We demonstrate that the modulation of current dACC activity by previous activity produces a behavioural adaptation that accelerates reactions to cues of similar difficulty to previous ones, and retards reactions to cues of different difficulty. Furthermore, this conflict adaptation, or Gratton effect, is abolished after surgically targeted ablation of the dACC. Our results demonstrate that the dACC provides a continuously updated prediction of expected cognitive demand to optimize future behavioural responses. In situations with stable cognitive demands, this signal promotes efficiency by hastening responses, but in situations with changing demands it engenders accuracy by delaying responses.

  • Document Type:
  • Collection(s):
  • Funding:
    1R01EY017658-01A/EY/NEI NIH HHS/United States
    1R01NS063249/NS/NINDS NIH HHS/United States
    5R01DP000339/DP/NCCDPHP CDC HHS/United States
    MH086400/MH/NIMH NIH HHS/United States
    P41RR14075/RR/NCRR NIH HHS/United States
    R01 DA026297/DA/NIDA NIH HHS/United States
    R01 EY017658/EY/NEI NIH HHS/United States
    R25 NS065743/NS/NINDS NIH HHS/United States
    R25NS065743/NS/NINDS NIH HHS/United States
    Howard Hughes Medical Institute/United States
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