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Mapping neural dynamics underlying saccade preparation and execution and their relation to reaction time and direction errors.
Bells, Sonya; Isabella, Silvia L; Brien, Donald C; Coe, Brian C; Munoz, Douglas P; Mabbott, Donald J; Cheyne, Douglas O.
Affiliation
  • Bells S; Program in Neurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
  • Isabella SL; Program in Neurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
  • Brien DC; Institute of Medical Sciences, Institute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
  • Coe BC; Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
  • Munoz DP; Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
  • Mabbott DJ; Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
  • Cheyne DO; Program in Neurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
Hum Brain Mapp ; 41(7): 1934-1949, 2020 05.
Article in En | MEDLINE | ID: mdl-31916374
ABSTRACT
Our ability to control and inhibit automatic behaviors is crucial for negotiating complex environments, all of which require rapid communication between sensory, motor, and cognitive networks. Here, we measured neuromagnetic brain activity to investigate the neural timing of cortical areas needed for inhibitory control, while 14 healthy young adults performed an interleaved prosaccade (look at a peripheral visual stimulus) and antisaccade (look away from stimulus) task. Analysis of how neural activity relates to saccade reaction time (SRT) and occurrence of direction errors (look at stimulus on antisaccade trials) provides insight into inhibitory control. Neuromagnetic source activity was used to extract stimulus-aligned and saccade-aligned activity to examine temporal differences between prosaccade and antisaccade trials in brain regions associated with saccade control. For stimulus-aligned antisaccade trials, a longer SRT was associated with delayed onset of neural activity within the ipsilateral parietal eye field (PEF) and bilateral frontal eye field (FEF). Saccade-aligned activity demonstrated peak activation 10ms before saccade-onset within the contralateral PEF for prosaccade trials and within the bilateral FEF for antisaccade trials. In addition, failure to inhibit prosaccades on anti-saccade trials was associated with increased activity prior to saccade onset within the FEF contralateral to the peripheral stimulus. This work on dynamic activity adds to our knowledge that direction errors were due, at least in part, to a failure to inhibit automatic prosaccades. These findings provide novel evidence in humans regarding the temporal dynamics within oculomotor areas needed for saccade programming and the role frontal brain regions have on top-down inhibitory control.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychomotor Performance / Reaction Time / Saccades / Nervous System Physiological Phenomena Limits: Adult / Female / Humans / Male Language: En Journal: Hum Brain Mapp Journal subject: CEREBRO Year: 2020 Type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psychomotor Performance / Reaction Time / Saccades / Nervous System Physiological Phenomena Limits: Adult / Female / Humans / Male Language: En Journal: Hum Brain Mapp Journal subject: CEREBRO Year: 2020 Type: Article Affiliation country: Canada