Representation of cardinal contour overlaps less with representation of nearby angles in cat visual cortex.

Extensive attempts have been made to explain the neurobiological basis of the greater sensitivity of the visual system to vertically or horizontally oriented information than to information presented at oblique angles. However, investigators have largely ignored the overlap of the representation of a given angle with the representation of nearby angles. Recordings based on intrinsic optical signals were obtained in area 17 from 12 adult cats during the presentation of contours in various orientations. A method investigating both amplitude and statistical significance of changes was proposed to evaluate the orientation tuning properties for cell populations in the central area retinotopically corresponding to 0-15 degrees of visual field. Cardinal orientations were found to activate significantly greater areas in the exposed cortical area than the areas activated by oblique orientations. Areas activated by cardinal or oblique contours and those separated from them by 10 degrees were compared. A significantly lower degree of overlap was seen between areas activated by presentation of cardinal contours and areas activated by neighboring orientations compared with those for oblique orientations which overlapped more extensively with neighboring orientations. In addition, areas activated only by cardinal contours were significantly larger than areas activated only by oblique contours. These results demonstrated in cell population level that more cells prefer horizontal or vertical orientations, and these cells are tuned more sharply than oblique selective cells.

[1]  K. Albus A quantitative study of the projection area of the central and the paracentral visual field in area 17 of the cat , 1975, Experimental Brain Research.

[2]  K. Albus,et al.  14C-Deoxyglucose mapping of orientation subunits in the cats visual cortical areas , 2004, Experimental Brain Research.

[3]  D. Hubel,et al.  Anatomical demonstration of orientation columns in macaque monkey , 1978, The Journal of comparative neurology.

[4]  Keiji Tanaka,et al.  Functional architecture in monkey inferotemporal cortex revealed by in vivo optical imaging , 1998, Neuroscience Research.

[5]  Keiji Tanaka,et al.  Effects of shape-discrimination training on the selectivity of inferotemporal cells in adult monkeys. , 1998, Journal of neurophysiology.

[6]  D. Fitzpatrick,et al.  Unequal representation of cardinal and oblique contours in ferret visual cortex. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[7]  H. Hirsch,et al.  Effects of early experience upon orientation sensitivity and binocularity of neurons in visual cortex of cats. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Amiram Grinvald,et al.  Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns , 1991, Nature.

[9]  M. Stryker,et al.  Development of Orientation Preference Maps in Ferret Primary Visual Cortex , 1996, The Journal of Neuroscience.

[10]  R. Bauer,et al.  Different anisotropies for texture and grating stimuli in the visual map of cat striate cortex , 1993, Vision Research.

[11]  K. Obermayer,et al.  Geometry of orientation and ocular dominance columns in monkey striate cortex , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  P. O. Bishop,et al.  Responses to moving slits by single units in cat striate cortex , 2004, Experimental Brain Research.

[13]  K. Albus A quantitative study of the projection area of the central and the paracentral visual field in area 17 of the cat , 1975, Experimental brain research.

[14]  C. Blakemore,et al.  An analysis of orientation selectivity in the cat's visual cortex , 1974, Experimental Brain Research.

[15]  D. Hubel,et al.  With 2 Plate and 20 Text-ftgutre8 Receptive Fields, Binocular Interaction and Functional Architecture in the Cat's Visual Cortex Cat Visual Cortex Part I Organization of Receptive Fields in Cat's Visual Cortex: Properties of 'simple' and 'complex' Fields Complex Receptive Fields , 2022 .

[16]  A. Grinvald,et al.  Relationships between orientation-preference pinwheels, cytochrome oxidase blobs, and ocular-dominance columns in primate striate cortex. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[17]  E. Switkes,et al.  Functional anatomy of macaque striate cortex. III. Color , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  Tobias Bonhoeffer,et al.  An Analysis of Orientation and Ocular Dominance Patterns in the Visual Cortex of Cats and Ferrets , 2000, Neural Computation.

[19]  K. Albus,et al.  On the spatial arrangement of iso-orientation bands in the cat's visual cortical areas 17 and 18: a 14C-Deoxyglucose study , 2004, Experimental Brain Research.

[20]  Keiji Tanaka,et al.  Optical Imaging of Functional Organization in the Monkey Inferotemporal Cortex , 1996, Science.

[21]  W. Singer Topographic organization of orientation columns in the cat visual cortex , 1981, Experimental Brain Research.

[22]  B R Payne,et al.  Functional organization of neurons in cat striate cortex: variations in preferred orientation and orientation selectivity with receptive-field type, ocular dominance, and location in visual-field map. , 1983, Journal of Neurophysiology.

[23]  D. Fitzpatrick,et al.  The contribution of sensory experience to the maturation of orientation selectivity in ferret visual cortex , 2001, Nature.

[24]  M. Sur,et al.  Stability of Cortical Responses and the Statistics of Natural Scenes , 2001, Neuron.

[25]  T. Bonhoeffer,et al.  Overrepresentation of horizontal and vertical orientation preferences in developing ferret area 17. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[26]  R. L. Valois,et al.  The orientation and direction selectivity of cells in macaque visual cortex , 1982, Vision Research.

[27]  G. Blasdel,et al.  Orientation selectivity, preference, and continuity in monkey striate cortex , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  G A Orban,et al.  Preferences for horizontal or vertical orientation in cat visual cortical neurones [proceedings]. , 1979, The Journal of physiology.

[29]  S. Ronner,et al.  Orientation anisotropy in monkey visual cortex , 1978, Brain Research.

[30]  Amir Shmuel,et al.  The spatial pattern of response magnitude and selectivity for orientation and direction in cat visual cortex. , 2003, Cerebral cortex.

[31]  E. Switkes,et al.  Functional anatomy of macaque striate cortex. II. Retinotopic organization , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  S. Appelle Perception and discrimination as a function of stimulus orientation: the "oblique effect" in man and animals. , 1972, Psychological bulletin.

[33]  E. Hoffmann,et al.  Membrane potential, chloride exchange, and chloride conductance in Ehrlich mouse ascites tumour cells. , 1979, The Journal of physiology.

[34]  M. Sur,et al.  Optically imaged maps of orientation preference in primary visual cortex of cats and ferrets , 1997, The Journal of comparative neurology.

[35]  Y. Frégnac,et al.  Early development of visual cortical cells in normal and dark‐reared kittens: relationship between orientation selectivity and ocular dominance. , 1978, The Journal of physiology.

[36]  A. Grinvald,et al.  A tandem-lens epifluorescence macroscope: Hundred-fold brightness advantage for wide-field imaging , 1991, Journal of Neuroscience Methods.