Monocularly Induced 2‐Deoxyglucose Patterns in the Visual Cortex and Lateral Geniculate Nucleus of the Cat: I. Anaesthetized and Paralysed Animals

Extending previous investigations of the topographic relationship between ocular dominance and orientation columns in the cat visual cortex the two systems were visualized with transneuronally transported [3H]proline and with activity‐dependent uptake of [14C]2‐deoxyglucose, respectively. In addition, we used the 2‐deoxyglucose method for a functional assay of both columnar systems. To this end, cats were injected with [3H]proline in the right eye. Two weeks later, they were stimulated monocularly through this eye by presenting contours of only a single orientation in the left and contours of many different orientations in the right visual hemifield while 2‐deoxyglucose was injected. The patterns of increased 2‐deoxyglucose uptake and of terminal labelling were analysed in flat‐mount sections of the visual cortices and in frontal sections of the lateral geniculate nuclei. In the lateral geniculate nucleus, regions of increased 2‐deoxyglucose uptake are in register with the [3H]proline‐labelled laminae of the open eye. In the visual cortex, the hemispheres stimulated with many different orientations showed a rather homogeneous accumulation of 2‐deoxyglucose over the entire extent and throughout all layers of area 17. The hemispheres stimulated with a single orientation displayed columnar patterns of orientation domains essentially similar to those obtained with binocular presentation of a single orientation. In particular and despite monocular stimulation, regions of increased 2‐deoxyglucose uptake were neither in register with the [3H]proline‐labelled terminals of the stimulated eye in layer IV nor confined to columns of neural tissue above and below these terminals. The maximal horizontal offset between the termination sites of thalamic afferents and activated orientation columns was in the order of 400 μm. These findings suggest several conclusions. (i) In the cat visual cortex, binocular convergence seems to occur so early in cortical processing that monocular stimulation with many orientations leads to a rather homogeneous activation of cortical tissue. (ii) From the termination zones of geniculate afferents activity is apparently distributed already within layer IV to the respective orientation columns. (iii) This horizontal spread of activity could be assured by target cells with radially extending dendrites and/or tangentially oriented fibres.

[1]  W Singer,et al.  Monocularly Induced 2‐Deoxyglucose Patterns in the Visual Cortex and Lateral Geniculate Nucleus of the Cat: II. Awake Animals and Strabismic Animals , 1993, The European journal of neuroscience.

[2]  W. Singer,et al.  Selection of intrinsic horizontal connections in the visual cortex by correlated neuronal activity. , 1992, Science.

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

[4]  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.

[5]  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.

[6]  W. Singer,et al.  Deoxyglucose mapping in the cat visual cortex following carotid artery injection and cortical flat-mounting , 1987, Journal of Neuroscience Methods.

[7]  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.

[8]  W. Singer,et al.  Topographic organization of the orientation column system in large flat‐mounts of the cat visual cortex: A 2‐deoxyglucose study , 1987, The Journal of comparative neurology.

[9]  G. Blasdel,et al.  Voltage-sensitive dyes reveal a modular organization in monkey striate cortex , 1986, Nature.

[10]  M. Sipser Frequency of dizygotic twinning , 1986, Nature.

[11]  R. Nudo,et al.  Stimulation‐induced [14C]2‐deoxyglucose labeling of synaptic activity in the central auditory system , 1986, The Journal of comparative neurology.

[12]  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.

[13]  N. Tumosa,et al.  [14C]2-Deoxyglucose demonstration of the organization of ocular dominance in areas 17 and 18 of the normal cat , 1983, Brain Research.

[14]  C. Blakemore,et al.  Development of orientation columns in cat striate cortex revealed by 2-deoxyglucose autoradiography , 1983, Nature.

[15]  C. Gilbert Microcircuitry of the visual cortex. , 1983, Annual review of neuroscience.

[16]  C. Blakemore,et al.  Ocular dominance columns in cat striate cortex and effects of monocular deprivation: a 2-deoxyglucose study. , 1983, Acta neurobiologiae experimentalis.

[17]  J. Lund,et al.  Widespread periodic intrinsic connections in the tree shrew visual cortex. , 1982, Science.

[18]  P. O. Bishop,et al.  Binocular interaction on monocularly discharged lateral geniculate and striate neurons in the cat. , 1981, Journal of neurophysiology.

[19]  M. Stryker,et al.  Physiological evidence that the 2-deoxyglucose method reveals orientation columns in cat visual cortex , 1981, Nature.

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

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

[22]  G. Henry,et al.  Anatomical organization of the primary visual cortex (area 17) of the cat. A comparison with area 17 of the macaque monkey , 1979, The Journal of comparative neurology.

[23]  T. Tsumoto Inhibitory and excitatory binocular convergence to visual cortical neurons of the cat , 1978, Brain Research.

[24]  M. Stryker,et al.  Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation. , 1978, The Journal of physiology.

[25]  S. Levay,et al.  Ocular dominance columns and their development in layer IV of the cat's visual cortex: A quantitative study , 1978, The Journal of comparative neurology.

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

[27]  D. Hubel,et al.  Orientation columns in macaque monkey visual cortex demonstrated by the 2-deoxyglucose autoradiographic technique , 1977, Nature.

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

[29]  M. Reivich,et al.  THE [14C]DEOXYGLUCOSE METHOD FOR THE MEASUREMENT OF LOCAL CEREBRAL GLUCOSE UTILIZATION: THEORY, PROCEDURE, AND NORMAL VALUES IN THE CONSCIOUS AND ANESTHETIZED ALBINO RAT 1 , 1977, Journal of neurochemistry.

[30]  M. Reivich,et al.  Metabolic mapping of the primary visual system of the monkey by means of the autoradiographic [14C]deoxyglucose technique. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[31]  C. Gilbert,et al.  Laminar patterns of geniculocortical projection in the cat , 1976, Brain Research.

[32]  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.

[33]  K. Albus Predominance of monocularly driven cells in the projection area of the central visual field in cat's striate cortex , 1975, Brain Research.

[34]  D. Hubel,et al.  Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey , 1972, The Journal of comparative neurology.

[35]  T. Powell,et al.  An experimental study of the termination of the lateral geniculo–cortical pathway in the cat and monkey , 1971, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[36]  B. Grafstein Transneuronal Transfer of Radioactivity in the Central Nervous System , 1971, Science.

[37]  D. Hubel,et al.  Anatomical Demonstration of Columns in the Monkey Striate Cortex , 1969, Nature.

[38]  S. W. Kuffler Discharge patterns and functional organization of mammalian retina. , 1953, Journal of neurophysiology.