Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-23T05:46:56.910Z Has data issue: false hasContentIssue false

Asymmetries in ON and OFF visual pathways of humans revealed using contrast-evoked cortical potentials

Published online by Cambridge University Press:  02 June 2009

Vance Zemon
Affiliation:
Laboratory of Biophysics, The Rockefeller University and Department of Psychology, Hunter College of the City University of New York
James Gordon
Affiliation:
Laboratory of Biophysics, The Rockefeller University and Department of Psychology, Hunter College of the City University of New York
Janet Welch
Affiliation:
Laboratory of Biophysics, The Rockefeller University and Department of Psychology, Hunter College of the City University of New York

Abstract

Positive- and negative-contrast stimuli yield the perceptions of brightness and darkness, respectively, and are processed separately by ON and OFF neural pathways. The properties of these morphologically and pharmacologically distinct subsystems were measured in humans by recording visual evoked potentials (VEPs). These electrical responses from the visual cortex were elicited by novel positive- and negative-contrast stimuli, designed to emphasize, selectively, contributions from ON and OFF pathways. Results revealed differential processing of the two types of contrast information, suggesting asymmetries in ON and OFF subsystems; OFF subsystems have finer spatial tuning and greater contrast gain than ON subsystems. These VEPs may be useful in diagnosing neurological disorders that involve primarily one subsystem.

Type
Short Communication
Copyright
Copyright © Cambridge University Press 1988

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Creutzfeldt, O.D. & Kuhnt, U. (1973). Electrophysiology and topographical distribution of visual evoked potentials in animals. In Handbook of Sensory Physiology, v. VII/3B, ed. Jung, R., pp. 595646. Berlin: Springer-Verlag.Google Scholar
De Valois, K.K. (1977). Independence of black and white: phase-specific adaptation. Vision Research 17, 209215.CrossRefGoogle ScholarPubMed
Devalois, R.L., Albrecht, D.G. & Thorell, L.G. (1982). Spatial frequency selectivity of cells in macaque visual cortex. Vision Research 11, 545559.CrossRefGoogle Scholar
Enroth-Cugell, C. & Robson, J.G. (1966). The contrast sensitivity of retinal ganglion cells of the cat. Journal of Physiology 187, 517552.CrossRefGoogle ScholarPubMed
Famiglietti, E.V. Jr. & Kolb, H. (1976). Structural basis for on- and off-center responses in retinal ganglion cells. Science 194, 193195.CrossRefGoogle ScholarPubMed
Hering, E. (1964). Outlines of a Theory of the Light Sense, translated by Hurwich, L.M. & Jameson, D., pp. 3031. Cambridge, Massachusetts: Harvard University Press.Google Scholar
Hubel, D.H. & Wiesel, T.N. (1961). Integrative action in the cat's lateral geniculate body. Journal of Physiology 155, 385398.CrossRefGoogle ScholarPubMed
Jasper, H.H. (1958). The 10–20 electrode system of the International Federation. Journal of Electroencephalography and Clinical Neu-rophysiology 10, 371375.Google Scholar
Jung, R. (1973). Visual perception and neurophysiology. In Handbook of Sensory Physiology, v. VII/3A, ed. Jung, R., pp. 1152. Berlin: Springer-Verlag.Google Scholar
Kaplan, E. & Shapley, R. (1982). X and Y cells in the lateral geniculate nucleus of macaque monkeys. Journal of Physiology 330, 125143.CrossRefGoogle ScholarPubMed
Kuffler, S. (1953). Discharge patterns and functional organization of mammalian retina. Journal of Neurophysiology 16, 3768.CrossRefGoogle ScholarPubMed
Magnussen, S. & Glad, A. (1975). Brightness and darkness enhancement during flicker: perceptual correlates of neuronal B- and D-systems in human vision. Experimental Brain Research 11, 399413.Google Scholar
Marozas, D.S. & May, D.C. (1985). Effects of figure-ground reversal on the visual-perceptual and visuo-motor performances of cerebral palsied and normal children. Perceptual and Motor Skills 60, 591598.CrossRefGoogle ScholarPubMed
May, D.C. (1978). Effects of color reversal of figure and ground drawing materials on drawing performance. Exceptional Children 44, 254260.CrossRefGoogle ScholarPubMed
Milkman, N., Schick, G., Rossetto, M., Ratliff, F., Shapley, R. & Victor, J. (1980). A two-dimensional computer-controlled visual stimulator. Behavioral Research Methods and Instrumentation 12, 283292.CrossRefGoogle Scholar
Movshon, J.A., Thompson, I.D. & Tolhurst, D.J. (1978). Spatial summation in the receptive fields of simple cells in the cat's striate cortex. Journal of Physiology 283, 5377.CrossRefGoogle ScholarPubMed
Nelson, R., Famiglietti, E.V. Jr. & Kolb, H. (1978). Intracellular staining reveals different levels of stratification for on- and off-center ganglion cells in cat retina. Journal of Neurophysiology 41, 472483.CrossRefGoogle ScholarPubMed
Schiller, P.H. (1982). Central connections of the retinal ON and OFF pathways. Nature 297, 580583.CrossRefGoogle ScholarPubMed
Schiller, P.H., Sandell, J.H. & Maunsell, J.H.R. (1986). Functions of the ON and OFF channels of the visual system. Nature 322, 824825.CrossRefGoogle ScholarPubMed
Shapley, R. & Gordon, J. (1985). Nonlinearity in the perception of form. Perception and Psychophysics 37, 8488.CrossRefGoogle ScholarPubMed
Sherk, H. & Horton, J.C. (1984). Receptive field properties in the cat's Area 17 in the absence of on-center geniculate input. Journal of Neuroscience 4, 381393.CrossRefGoogle ScholarPubMed
Slaughter, M.M. & Miller, R.F. (1981). 2-amino-4-phosphono- butyric acid: a new pharmacological tool for retina research. Science 211, 182184.CrossRefGoogle Scholar
Spekreijse, H. & Oosting, H. (1970). Linearizing: a method for analysing and synthesizing nonlinear systems. Kybernetik 7, 2231.CrossRefGoogle ScholarPubMed
Spitzer, H. & Hochstein, S. (1985). Simple- and complex-cell response dependences on stimulation parameters. Journal of Neurophysiology 53, 12441265.CrossRefGoogle ScholarPubMed
Tranchina, D., Gordon, J., Shapley, R. & Toyoda, J. (1981). Linear information processing in the retina: a study of horizontal cell responses. Proceedings of the National Academy of Sciences 78, 65406542.CrossRefGoogle ScholarPubMed
Uhlin, D.M. & Dickson, J.D. (1970). The effect of figure-ground reversal in the H-T-P drawings of spastic cerebral palsied children. Journal of Clinical Psychology 26, 8788.3.0.CO;2-Q>CrossRefGoogle ScholarPubMed
Von Helmholtz, H. (1962). Helmholtz's Treatise on Physiological Optics, Vol. 2, ed. Southall, J., pp. 186. New York: Dover Press. Translated from the 3rd German edition, 1911.Google Scholar
Zemon, V., Kaplan, E. & Ratliff, F. (1986). In Frontiers of Clinical Neuroscience, v. 3: Evoked Potentials, ed. Cracco, R.Q. & Bodis-Wollner, I., pp. 287295. New York: Alan R. Liss.Google Scholar
Zemon, V. & Ratliff, F. (1984). Intermodulation components of the visual evoked potential: responses to lateral and superimposed stimuli. Biological Cybernetics 50, 401408.CrossRefGoogle ScholarPubMed