Retinotopic and nonretinotopic field potentials in cat visual cortex

Abstract Two types of field potentials were identified in cat visual cortex using contrast reversal of oriented bar gratings: a short-latency fast-local component with a retinotopic organization similar to that seen with single-unit discharges at the same cortical site, and a slow, nonretinotopic component with a longer peak latency. The slow-distributed component had an extensive receptive field mapped by measuring the amplitude of binary kernels and showed strong inhibitory interactions within the receptive field. The peak latency of the slow-local component increased with distance from the retinotopic center, suggesting a possible conduction delay. Both components showed some orientation bias depending on the laminar location, but the bias could be independent of the orientation preferred by single units in the immediate vicinity. The present findings indicate that locally generated field potentials reflect cortical mechanisms for nonlinear integration over wide areas of the visual field.

[1]  K. Albus,et al.  Structural and Functional Organization of the Neocortex , 1994 .

[2]  B. Connors,et al.  Regenerative activity in apical dendrites of pyramidal cells in neocortex. , 1993, Cerebral cortex.

[3]  D. Heeger Half-squaring in responses of cat striate cells , 1992, Visual Neuroscience.

[4]  R Gattass,et al.  Dynamic surrounds of receptive fields in primate striate cortex: a physiological basis for perceptual completion? , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[5]  D. Heeger Normalization of cell responses in cat striate cortex , 1992, Visual Neuroscience.

[6]  T. H. Brown,et al.  Dendritic spines: convergence of theory and experiment. , 1992, Science.

[7]  D. V. van Essen,et al.  Neuronal responses to static texture patterns in area V1 of the alert macaque monkey. , 1992, Journal of neurophysiology.

[8]  Erich E. Sutter,et al.  The field topography of ERG components in man—I. The photopic luminance response , 1992, Vision Research.

[9]  D C Van Essen,et al.  Information processing in the primate visual system: an integrated systems perspective. , 1992, Science.

[10]  Robert J. Snowden,et al.  Subtractive and divisive adaptation in the human visual system , 1992, Nature.

[11]  Ee Sutter,et al.  A deterministic approach to nonlinear systems analysis , 1992 .

[12]  R. B. Pinter,et al.  Nonlinear Vision: Determination of Neural Receptive Fields, Function, and Networks , 1992 .

[13]  Mark W. Cannon,et al.  Spatial interactions in apparent contrast: Inhibitory effects among grating patterns of different spatial frequencies, spatial positions and orientations , 1991, Vision Research.

[14]  Tribhawan Kumar,et al.  Influence of remote objects on local depth perception , 1991, Vision Research.

[15]  J. Bolz,et al.  Functional specificity of a long-range horizontal connection in cat visual cortex: a cross-correlation study , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  H. Tamura,et al.  Horizontal interactions between visual cortical neurones studied by cross‐correlation analysis in the cat. , 1991, The Journal of physiology.

[17]  Erich E. Sutter,et al.  The Fast m-Transform: A Fast Computation of Cross-Correlations with Binary m-Sequences , 1991, SIAM J. Comput..

[18]  C. Gilbert,et al.  Synaptic physiology of horizontal connections in the cat's visual cortex , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  T. Kasamatsu,et al.  Cortical recovery from effects of monocular deprivation caused by diffusion and occlusion , 1991, Brain Research.

[20]  T. Wiesel,et al.  Targets of horizontal connections in macaque primary visual cortex , 1991, The Journal of comparative neurology.

[21]  K. Stratford,et al.  Synaptic transmission between individual pyramidal neurons of the rat visual cortex in vitro , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[22]  E. Fetz,et al.  Synaptic Interactions between Cortical Neurons , 1991 .

[23]  O Herreras,et al.  Propagating dendritic action potential mediates synaptic transmission in CA1 pyramidal cells in situ. , 1990, Journal of neurophysiology.

[24]  W. Singer,et al.  Horizontal Interactions in Cat Striate Cortex: II. A Current Source‐Density Analysis , 1990, The European journal of neuroscience.

[25]  H. J. Luhmann,et al.  Horizontal Interactions in Cat Striate Cortex: I. Anatomical Substrate and Postnatal Development , 1990, The European journal of neuroscience.

[26]  Charles D. Gilbert,et al.  Lateral interactions in visual cortex. , 1990, Cold Spring Harbor symposia on quantitative biology.

[27]  H. Berg Cold Spring Harbor Symposia on Quantitative Biology.: Vol. LII. Evolution of Catalytic Functions. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 1987, ISBN 0-87969-054-2, xix + 955 pp., US $150.00. , 1989 .

[28]  J. Barker,et al.  Localization of tetrodotoxin-sensitive field potentials of CA1 pyramidal cells in the rat hippocampus. , 1989, Journal of neurophysiology.

[29]  T. Wiesel,et al.  Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[30]  R. von der Heydt,et al.  Mechanisms of contour perception in monkey visual cortex. I. Lines of pattern discontinuity , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[31]  D. Prince,et al.  Sodium channels in dendrites of rat cortical pyramidal neurons. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[32]  R. C. Van Sluyters,et al.  The overall pattern of ocular dominance bands in cat visual cortex , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  C. Blakemore,et al.  The organization of corticocortical projections from area 17 to area 18 of the cat’s visual cortex , 1988, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[34]  M. Cynader,et al.  Anatomical properties and physiological correlates of the intrinsic connections in cat area 18 , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  P Anderson,et al.  Thresholds of action potentials evoked by synapses on the dendrites of pyramidal cells in the rat hippocampus in vitro. , 1987, The Journal of physiology.

[36]  David C. Burr,et al.  Evidence for the existence and development of visual inhibition in humans , 1986, Nature.

[37]  T. Wiesel,et al.  Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[38]  U. Mitzdorf,et al.  The physiological causes of VEP: current source density analysis of electrically and visually evoked potentials , 1986 .

[39]  G. Innocenti General Organization of Callosal Connections in the Cerebral Cortex , 1986 .

[40]  M. Cynader,et al.  Intrinsic projections within visual cortex: evidence for orientation-specific local connections. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[41]  U. Mitzdorf Current source-density method and application in cat cerebral cortex: investigation of evoked potentials and EEG phenomena. , 1985, Physiological reviews.

[42]  J. Allman,et al.  Stimulus specific responses from beyond the classical receptive field: neurophysiological mechanisms for local-global comparisons in visual neurons. , 1985, Annual review of neuroscience.

[43]  J Bullier,et al.  Branching and laminar origin of projections between visual cortical areas in the cat , 1984, The Journal of comparative neurology.

[44]  D. Whitteridge,et al.  Form, function and intracortical projections of spiny neurones in the striate visual cortex of the cat. , 1984, The Journal of physiology.

[45]  D. Prince,et al.  Synaptic control of excitability in isolated dendrites of hippocampal neurons , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  John H. R. Maunsell,et al.  Hierarchical organization and functional streams in the visual cortex , 1983, Trends in Neurosciences.

[47]  E H Land,et al.  Recent advances in retinex theory and some implications for cortical computations: color vision and the natural image. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[48]  J. Lund,et al.  Intrinsic laminar lattice connections in primate visual cortex , 1983, The Journal of comparative neurology.

[49]  T. Wiesel,et al.  Clustered intrinsic connections in cat visual cortex , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  A. L. Humphrey,et al.  Anatomical banding of intrinsic connections in striate cortex of tree shrews (Tupaia glis) , 1982, The Journal of comparative neurology.

[51]  John S. Ebersole,et al.  Intracortical evoked potentials of cats elicited by punctate visual stimuli in receptive field peripheries , 1981, Brain Research.

[52]  D. Mackay,et al.  Modulatory influences of moving textured backgrounds on responsiveness of simple cells in feline striate cortex , 1981, The Journal of physiology.

[53]  K. Tanaka,et al.  Cross-Correlation Analysis of Interneuronal Connectivity in cat visual cortex. , 1981, Journal of neurophysiology.

[54]  K. Tanaka,et al.  Organization of cat visual cortex as investigated by cross-correlation technique. , 1981, Journal of neurophysiology.

[55]  N. Bowery,et al.  3H-baclofen and 3H-GABA bind to bicuculline-insensitive GABAB sites in rat brain , 1981, Nature.

[56]  R. Llinás,et al.  Electrophysiological properties of in vitro Purkinje cell dendrites in mammalian cerebellar slices. , 1980, The Journal of physiology.

[57]  A. Treisman,et al.  A feature-integration theory of attention , 1980, Cognitive Psychology.

[58]  D. W. Heeley A perceived spatial frequency shift at orientations orthogonal to adapting gratings , 1979, Vision Research.

[59]  M. Wong-Riley Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry , 1979, Brain Research.

[60]  T. Wiesel,et al.  Morphology and intracortical projections of functionally characterised neurones in the cat visual cortex , 1979, Nature.

[61]  P. Lennie,et al.  The mechanism of peripherally evoked responses in retinal ganglion cells. , 1979, The Journal of physiology.

[62]  D. Prince,et al.  Intradendritic recordings from hippocampal neurons. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[63]  L. Palmer,et al.  The retinotopic organization of area 17 (striate cortex) in the cat , 1978, The Journal of comparative neurology.

[64]  J. Nelson,et al.  Orientation-selective inhibition from beyond the classic visual receptive field , 1978, Brain Research.

[65]  K. Albus,et al.  Effects of interacting visual patterns on single cell responses in cat's striate cortex , 1977, Vision Research.

[66]  T. Wiesel,et al.  The distribution of afferents representing the right and left eyes in the cat's visual cortex , 1977, Brain Research.

[67]  H. Barlow,et al.  The effects of remote retinal stimulation on the responses of cat retinal ganglion cells. , 1977, The Journal of physiology.

[68]  L. Maffei,et al.  The unresponsive regions of visual cortical receptive fields , 1976, Vision Research.

[69]  R. Shapley,et al.  Linear and nonlinear spatial subunits in Y cat retinal ganglion cells. , 1976, The Journal of physiology.

[70]  T. Powell,et al.  The intrinsic, association and commissural connections of area 17 on the visual cortex. , 1975, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[71]  J T McIlwain,et al.  Visual receptive fields and their images in superior colliculus of the cat. , 1975, Journal of neurophysiology.

[72]  B. Fischer,et al.  Quantitative aspects of the shift-effect in cat retinal ganglion cells , 1975, Brain Research.

[73]  D. Hubel,et al.  Uniformity of monkey striate cortex: A parallel relationship between field size, scatter, and magnification factor , 1974, The Journal of comparative neurology.

[74]  B. Fischer Overlap of receptive field centers and representation of the visual field in the cat's optic tract. , 1973, Vision research.

[75]  P. O. Bishop,et al.  Receptive fields of simple cells in the cat striate cortex , 1973, The Journal of physiology.

[76]  H Ikeda,et al.  Functional organization of the periphery effect in retinal ganglion cells. , 1972, Vision research.

[77]  B. H. Jones Responses of single neurons in cat visual cortex to a simple and a more complex stimulus. , 1970, The American journal of physiology.

[78]  M. Ito,et al.  Visual evoked response of single cells and of the EEG in primary visual area of the cat. , 1969, Journal of neurophysiology.

[79]  P. O. Bishop,et al.  Residual eye movements in receptive-field studies of paralyzed cats. , 1967, Vision research.

[80]  B. Boycott,et al.  Organization of the primate retina: electron microscopy , 1966, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[81]  W. Levick,et al.  EVIDENCE THAT MCILWAIN'S PERIPHERY EFFECT IS NOT A STRAY LIGHT ARTIFACT. , 1965, Journal of neurophysiology.

[82]  D H HUBEL,et al.  RECEPTIVE FIELDS AND FUNCTIONAL ARCHITECTURE IN TWO NONSTRIATE VISUAL AREAS (18 AND 19) OF THE CAT. , 1965, Journal of neurophysiology.

[83]  J. Mcilwain RECEPTIVE FIELDS OF OPTIC TRACT AXONS AND LATERAL GENICULATE CELLS: PERIPHERAL EXTENT AND BARBITURATE SENSITIVITY. , 1964, Journal of neurophysiology.

[84]  A. Cowey PROJECTION OF THE RETINA ON TO STRIATE AND PRESTRIATE CORTEX IN THE SQUIRREL MONKEY, SAIMIRI SCIUREUS. , 1964, Journal of neurophysiology.

[85]  D. Hubel,et al.  Receptive fields, binocular interaction and functional architecture in the cat's visual cortex , 1962, The Journal of physiology.

[86]  R. Doty,et al.  Potentials evoked in cat cerebral cortex by diffuse and by punctiform photic stimuli. , 1958, Journal of neurophysiology.