Spatial and temporal properties of X and Y cells in the cat lateral geniculate nucleus.

1. Extracellular recordings were obtained from units in the dorsal lateral geniculate nucleus of anaesthetized cats. 2. Of sixty‐nine units, sixty‐three could be unambiguously identified as either X (n = 33) or Y (n = 30) by testing the presence of a null response to stationary sine wave gratings presented in different spatial phases. 3. In response to stationary gratings flashed on and off, Y cells exhibited bigger, more transient responses than X cells. 4. All Y cells but few X cells exhibited a shift effect (modulated periphery effect). 5. In response to drifting sine wave gratings of different spatial frequencies, X cells preferred higher spatial frequencies and showed smaller peak contrast sensitivities and somewhat narrower tuning curves than Y cells. 6. In response to a sine wave grafting of optimal spatial frequency drifting at different velocities, X and Y cells had similar temporal tuning curves. However, Y cells, largely because they preferred lower spatial frequencies, preferred higher drift velocities than X cells. 7. Our data suggest that X and Y cells can be differentiated objectively on the basis of a number of discharge parameters. These parameters are compared with similar data collected by others from neurones in the visual cortex.

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

[2]  G. B. Wetherill,et al.  SEQUENTIAL ESTIMATION OF POINTS ON A PSYCHOMETRIC FUNCTION. , 1965, The British journal of mathematical and statistical psychology.

[3]  C. Enroth-Cugell,et al.  The contrast sensitivity of retinal ganglion cells of the cat , 1966, The Journal of physiology.

[4]  D. M. MACKAY,et al.  Elevation of Visual Threshold by Displacement of Retinal Image , 1970, Nature.

[5]  K. Sanderson,et al.  The projection of the visual field to the lateral geniculate and medial interlaminar nuclei in the cat , 1971, The Journal of comparative neurology.

[6]  J. Stone,et al.  Conduction velocity of afferents to cat visual cortex: a correlation with cortical receptive field properties. , 1971, Brain research.

[7]  W. Levick,et al.  Sustained and transient neurones in the cat's retina and lateral geniculate nucleus , 1971, The Journal of physiology.

[8]  H Ikeda,et al.  Receptive field organization of ‘sustained’ and ‘transient’ retinal ganglion cells which subserve different functional roles , 1972, The Journal of physiology.

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

[10]  J. Stone,et al.  Relay of receptive-field properties in dorsal lateral geniculate nucleus of the cat. , 1972, Journal of neurophysiology.

[11]  J. Stone,et al.  Projection of X- and Y-cells of the cat's lateral geniculate nucleus to areas 17 and 18 of visual cortex. , 1973, Journal of neurophysiology.

[12]  W. Levick,et al.  Properties of sustained and transient ganglion cells in the cat retina , 1973, The Journal of physiology.

[13]  B. Dreher,et al.  Receptive field analysis: responses to moving visual contours by single lateral geniculate neurones in the cat , 1973, The Journal of physiology.

[14]  W. Levick,et al.  Brisk and sluggish concentrically organized ganglion cells in the cat's retina , 1974, The Journal of physiology.

[15]  ROBERT SHAPLEY,et al.  Visual spatial summation in two classes of geniculate cells , 1975, Nature.

[16]  H. Noda,et al.  Discharges of relay cells in lateral geniculate nucleus of the cat during spontaneous eye movements in light and darkness. , 1975, The Journal of physiology.

[17]  W. Singer,et al.  Organization of cat striate cortex: a correlation of receptive-field properties with afferent and efferent connections. , 1975, Journal of neurophysiology.

[18]  B. A. Brooks,et al.  Influence of stimulus parameters on visual sensitivity during saccadic eye movement , 1975, Vision Research.

[19]  R. Shapley,et al.  Quantitative analysis of retinal ganglion cell classifications. , 1976, The Journal of physiology.

[20]  J. Stone,et al.  Properties of relay cells in cat's lateral geniculate nucleus: a comparison of W-cells with X- and Y-cells. , 1976, Journal of neurophysiology.

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

[22]  Klaus-Peter Hoffmann,et al.  Interlaminar differences in the effects of early and late monocular deprivation on the visual acuity of cells in the lateral geniculate nucleus of the cat , 1977, Neuroscience Letters.

[23]  The shift-effect in the cat's lateral geniculate neurons , 1974, Experimental Brain Research.

[24]  Interaction of receptive field responses and shift-effect in cat retinal and geniculate neurons , 1978, Experimental Brain Research.

[25]  M. Wright,et al.  Spatial and temporal properties of ‘sustained’ and ‘transient’ neurones in area 17 of the cat's visual cortex , 1975, Experimental Brain Research.

[26]  The shift-effect in the lateral geniculate body of the rhesus monkey , 1977, Experimental Brain Research.

[27]  W. R. Levick,et al.  Another tungsten microelectrode , 1972, Medical and biological engineering.