• Title of article

    The effect of spatial frequency on chromatic and achromatic steady-state visual evoked potentials

  • Author/Authors

    Kenji Arakawa، نويسنده , , Shozo Tobimatsu، نويسنده , , Hiroyuki Tomoda، نويسنده , , Jun-ichi Kira، نويسنده , , Motohiro Kato، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1999
  • Pages
    6
  • From page
    1959
  • To page
    1964
  • Abstract
    Objective: Little is known about the physiological properties of the major components of steady-state visual evoked potentials (VEPs). Based on the hypothesis that isoluminant color and high contrast pattern differentially activate the parvo- and magnocellular pathways, we studied difference in spatial frequency function between chromatic and achromatic VEPs to sinusoidal gratings. Methods: Steady-state VEPs to isoluminant chromatic (red-green) and high contrast (90%) achromatic (black-white) sinusoidal gratings with nine spatial frequencies (0.5 to 8.0 cycles/° (cpd)) at 4 Hz (8 reversals/s) were recorded in 13 normal subjects. VEPs were Fourier analyzed to obtain phase and amplitude of the second (2F) and fourth (4F) harmonic responses. Results: The 2F amplitude of chromatic VEPs decreased above 4.0 cpd in a low-pass function while that of achromatic VEPs showed a band-pass function with a peak at 4.0 cpd. The 4F amplitude of chromatic VEPs was not affected significantly by spatial frequency whereas that of achromatic VEPs exhibited a high-pass function. The phases of 2F and 4F showed a non-monotonic function of spatial frequency in both chromatic and achromatic stimuli with peaks at middle spatial frequencies. Conclusion: Chromatic and achromatic visual stimuli differently affected 2F and 4F components, which thus suggests that 2F and 4F components are generated from different neuronal subgroups largely in the parvocellular pathway.
  • Keywords
    Color and luminance , Pattern visual evoked potentials , Steady-state , Harmonic components , Spatial frequency
  • Journal title
    Clinical Neurophysiology
  • Serial Year
    1999
  • Journal title
    Clinical Neurophysiology
  • Record number

    521770