October 2003
Volume 3, Issue 9
Free
Vision Sciences Society Annual Meeting Abstract  |   October 2003
Event-related fMRI of saccadic response inhibition
Author Affiliations
  • Mark W Greenlee
    University of Oldenburg, Germany
Journal of Vision October 2003, Vol.3, 697. doi:https://doi.org/10.1167/3.9.697
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Mark W Greenlee, Jale Oezyurt, Roland M Rutschmann, Ignacio Vallines; Event-related fMRI of saccadic response inhibition. Journal of Vision 2003;3(9):697. https://doi.org/10.1167/3.9.697.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Inhibition of on-going or planned movements as well as monitoring errors is essential for adaptation to changing environments. We performed event-related functional MRI to examine neural correlates of inhibition and error processing in a saccadic Go/NoGo task. Contrary to the procedure in block designs, the BOLD response is recorded in each trial type separately, thus allowing us to sort trials depending on whether the trial was correct or incorrect. Gradient-echo EPI was performed on a 1.5 T scanner with a TR of 3 sec and 24 slices. Saccades and fixations were monitored using the MR-Eyetacker. Results from 7 subjects reveal NoGo dominant activity in dorsolateral prefrontal cortex (BA 9, 10, 46) and in the anterior cingulate (BA 24). Errors of commission on NoGo trials evoked stronger activation in right frontal operculum (BA 47), right DLPF (BA 9) and left orbiofrontal (BA 11) cortex compared to that found in Go trials.

Greenlee, M. W., Oezyurt, J., Rutschmann, R. M., Vallines, I.(2003). Event-related fMRI of saccadic response inhibition [Abstract]. Journal of Vision, 3( 9): 697, 697a, http://journalofvision.org/3/9/697/, doi:10.1167/3.9.697. [CrossRef]
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×