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Effects of ON channel blockade with 2-amino-4-phosphonobutyrate (APB) on brightness and contrast perception in monkeys

Published online by Cambridge University Press:  02 June 2009

Robert P. Dolan
Affiliation:
Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology,
Peter H. Schiller
Affiliation:
Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology,

Abstract

Four experiments were performed to assess the effects of ON channel blockade with the glutamate analog 2-amino-4-phosphonobutyrate (APB) on brightness and contrast perception in monkeys. In Experiment 1, we demonstrate that stimuli brighter than background (incremental stimuli) appear less bright following ON channel blockade. This decrease in brightness is not enough to account for the previously observed threshold increase for detection of incremental stimuli following APB administration (Schiller et al., 1986; Dolan & Schiller, 1989). Experiment 2 examines the role of the ON and OFF channels in the interaction between local contrast and apparent brightness. The phenomenon of simultaneous contrast was examined under normal conditions and following APB administration. We find that even following ON channel blockade, the brightness of a stimulus is determined primarily by its contrast with its immediate background. This indicates that the lateral processes involved in simultaneous contrast can operate even when one channel has been compromised. In Experiment 3, we examined the role of the ON channel in detection of stimuli that appear by virtue of changes in background vs. foreground luminance. We find that the ON channel selectively conveys information pertaining not only to the temporal nature that defines the stimulus as incremental but also to the spatial features that define it as incremental. In Experiment 4, we test the hypothesis that incremental and decremental temporal luminance ramps are differentially processed by the ON and OFF channels to a higher degree than are step-luminance changes. We find that the detection of incremental ramps is no more affected than is the detection of incremental steps following APB administration.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1994

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References

Anstis, S.M. (1967). Visual adaptation to gradual change of intensity. Science 155, 710712.CrossRefGoogle ScholarPubMed
Arkin, M.S. & Miller, R.F. (1987). Subtle actions of 2-amino-4-phosphonobutyrate (APB) on the OFF pathway in the mudpuppy retina. Brain Research 426, 142148.CrossRefGoogle ScholarPubMed
Bolz, J., Wässle, H. & Thier, P. (1984). Pharmacological modulation of ON and OFF ganglion cells in the cat retina. Neuroscience 12(3), 875885.CrossRefGoogle Scholar
Broca, A. & Sulzer, D. (1902). La sensation lumineuse en fonction du temps. Journal de Physiologie el Pathologie Générale 4, 632640.Google Scholar
Cavanagh, P. & Anstis, S.M. (1986). Brightness shift in drifting ramp gratings isolates a transient mechanism. Vision Research 26(6), 899908.CrossRefGoogle ScholarPubMed
Dolan, R.P. (1992). ON and OFF channels in primate vision. M.I.T. Doctoral Thesis.Google Scholar
Dolan, R.P. & Schiller, P.H. (1989). Evidence for only depolarizing rod bipolar cells in the primate retina. Visual Neuroscience 2, 421424.CrossRefGoogle ScholarPubMed
Hanly, M. & MacKay, D.M. (1979). Polarity-sensitive perceptual adaptation to temporal sawtooth modulation of luminance. Experimental Brain Research 35, 3746.CrossRefGoogle ScholarPubMed
Horton, J.C. & Sherk, H. (1984). Receptive-field properties of the cat’s lateral geniculate nucleus in the absence of retinal ON-center input. Journal of Neuroscience 4, 374380.CrossRefGoogle ScholarPubMed
Jung, R. (1973). Visual perception and neurophysiology. In Handbook of Sensory Physiology, Vol. VII/3: Central Processing of Visual Information A: Integrative Functions and Comparative Data, ed. Autrum, R., Jung, R., Loewenstein, W., MacKay, D.M. & Teuber, H.L., pp. 1152. Berlin, Heidelberg, New York: Springer-Verlag.Google Scholar
Knapp, A.G. & Mistler, L.A. (1983). Response properties of cells in rabbit’s lateral geniculate nucleus during reversible blockade of retinal ON-center channel. Journal of Neurophysiology 50, 12361245.CrossRefGoogle ScholarPubMed
Knapp, A.G. & Schiller, P.H. (1984). The contribution of ON-bipolar cells to the electroretinogram of rabbits and monkeys: A study using 2-amino-4-phosphonobutyrate (APB). Vision Research 24(12), 18411846.CrossRefGoogle Scholar
Krauskopf, J. (1980). Discrimination and detection of changes in luminance. Vision Research 20, 671677.CrossRefGoogle ScholarPubMed
Kuffler, S.W. (1953). Discharge patterns and functional organization of mammalian retina. Journal of Neurophysiology 16, 3768.CrossRefGoogle ScholarPubMed
Levick, W.R. (1973). Maintained discharge in the visual system and its role in information processing. In Handbook of Sensory Physiology, Vol. VII/3: Central Processing of Visual Information A: Integrative Functions and Comparative Data, ed. Autrum, R., Jung, R., Loewenstein, W., MacKay, D.M. & Teuber, H.L., pp. 575598. Berlin, Heidelberg, New York: Springer-Verlag.Google Scholar
Levine, M.W. & Shefner, J.M. (1977). Variability in ganglion cell firing patterns: Implications for separate “ON” and “OFF” processes. Vision Research 17, 765776.CrossRefGoogle Scholar
Magnussen, S. & Glad, A. (1975). Brightness and darkness enhancement during flicker: Perceptual correlates of neuronal B- and D-sys-tems in human vision. Experimental Brain Research 22, 399413.CrossRefGoogle Scholar
Massey, S.C., Redburn, D.A. & Crawford, M.J.L. (1983). The effects of 2-amino-4-phosphonobutyric acid (APB) on the ERG and ganglion cell discharge of rabbit retina. Vision Research 23, 16071613.CrossRefGoogle ScholarPubMed
McGuire, B.A., Stevens, J.K. & Sterling, P. (1984). Microcircuitry of bipolar cells in cat retina. Journal of Neuroscience 4, 29202938.CrossRefGoogle ScholarPubMed
Savoy, R.L. & Burns, M.M. (1989). Isolated cone classes and the dis-embodied edge: New stimuli for psychophysics and neurophysiology. Investigative Ophthalmology and Visual Science (Suppl.) 30, 220.Google Scholar
Schiller, P.H. (1982). Central connections of the retinal ON and OFF pathways. Nature 297, 580583.CrossRefGoogle ScholarPubMed
Schiller, P.H. (1984). The connections of the retinal ON and OFF pathways to the lateral geniculate nucleus of the monkey. Vision Research 24(9), 923932.CrossRefGoogle Scholar
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
Sherk, H. & Horton, J.C. (1984). Receptive-field properties in cat’s area 17 in the absence of ON-center geniculate input. Journal of Neuroscience 4, 381393.CrossRefGoogle ScholarPubMed
Shiells, R.A., Falk, G. & Naghshineh, S. (1981). Action of glutamate and aspartate analogues on rod horizontal and bipolar cells. Nature 294, 592594.CrossRefGoogle ScholarPubMed
Slaughter, M.M. & Miller, R.F. (1981). 2-amino-4-phosphonobutyric acid: A new pharmacological tool for retina research. Science 211, 182184.CrossRefGoogle ScholarPubMed