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Adaptation of visually evoked responses of relay cells in the dorsal lateral geniculate nucleus of the cat following prolonged exposure to drifting gratings

Published online by Cambridge University Press:  02 June 2009

Tiande Shou
Affiliation:
Vision Research Laboratory, Department of Biology, University of Science and Technology of China Hefei, Anhui 230027, P.R., China Beijing Laboratory of Cognitive Science, USTC, Chinese Academy of Sciences, Beijing 100039, P.R., China
Xiangrui Li
Affiliation:
Vision Research Laboratory, Department of Biology, University of Science and Technology of China Hefei, Anhui 230027, P.R., China
Yifeng Zhou
Affiliation:
Vision Research Laboratory, Department of Biology, University of Science and Technology of China Hefei, Anhui 230027, P.R., China Beijing Laboratory of Cognitive Science, USTC, Chinese Academy of Sciences, Beijing 100039, P.R., China
Bing Hu
Affiliation:
Vision Research Laboratory, Department of Biology, University of Science and Technology of China Hefei, Anhui 230027, P.R., China

Abstract

Adaptation of visual cortical cells' responses is observed following repeated presentation of grating stimuli. Grating adaptation is believed to exist only at the cortical level. The purpose of this study was to see if grating adaptation also occurs in the lateral geniculate nucleus. We studied the responses of 164 relay cells in layer A and A1 of the dorsal lateral geniculate nucleus (LGNd) to grating stimuli. Normal cats, as well as cats in which visual cortex was ablated, were studied. Adaptation was investigated using repeated presentation of gratings of different contrasts and orientations. The results showed the following: (1) Grating adaptation reduced the responses of 46% of the LGNd cells recorded. The responses normally decreased within 30 s and then stabilized. However, there was heterogeneity in the effects observed. About 38% of the cells studied were not affected by the adapting gratings. Some cells (16%) showed facilitation rather than habituation of their responses to test stimuli. (2) There was no significant difference between X and Y cells in their susceptibility to adaptation. This suggests that grating adaptation is a general property, independent of cell type. (3) The contrast-response curves of 57% of the LGNd cells studied shifted down after exposure to high-contrast adapting gratings. (4) Adapting gratings of the cells' preferred orientation decreased the orientation sensitivity of 56% of the orientation-sensitive cells. Adapting gratings at the nonpreferred orientation did not affect orientation sensitivity. (5) Prolonged grating adaptation also reduced the responses of 49% of the LGNd cells after inactivation of cortical inputs to the LGNd.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1996

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References

Albrecht, D.G., Farrar, S.B. & Hamilton, D.B. (1984). Spatial contrast adaptation characteristics of neurones recorded in the cat's visual cortex. Journal of Physiology 347, 713739.CrossRefGoogle ScholarPubMed
Batschelet, E. (1981). Circular Statistics in Biology. New York: Academic Press.Google Scholar
Blake, R. & Fox, R. (1974). Adaptation to invisible gratings and the site of binocular rivalry suppression. Nature 249, 488490.CrossRefGoogle ScholarPubMed
Blakemore, C. & Campbell, F.W. (1969). On the existence of neurones in the human visual system selectively sensitive to the orientation and size of retinal images. Journal of Physiology 203, 237260.CrossRefGoogle Scholar
Blakemore, C. & Campbell, F.W. (1986). Adaptation to spatial stimuli. Journal of Physiology 200, 1113.Google Scholar
Cleland, B.G. & Levick, W.R. (1974). Brisk and sluggish concentrically organized ganglion cells in the cat's retina. Journal of Physiology 162, 403431.Google Scholar
Creutzfeldt, O.D., Garey, L.J., Card, R. & Wolff, J.R. (1977). The distribution of degenerating axons after small lesions in the intact and isolated visual cortex of the cat. Experimental Brain Research 27, 419440.Google Scholar
Daniels, J.D., Norman, J.L. & Pettigrew, J.D. (1977). Biases for oriented moving bars in lateral geniculate nucleus neurons of normal and stripe-reared cats. Experimental Brain Research 29, 155172.Google Scholar
Debruyn, E.J. & Bonds, A.B. (1986). Contrast adaptation in cat visual cortex is not mediated by GABA. Brain Research 383, 339342.CrossRefGoogle Scholar
Enroth-Cugell, C. & Robson, J.G. (1966). The contrast sensitivity of retinal ganglion cells of the cat. Journal of Physiology 187, 517552.Google Scholar
Fisken, R.A., Garey, L.J. & Powell, T.P.S. (1975). The intrinsic association and commissural connections of area 17 of the visual cortex. Philosophical Transactions of the Royal Society 272, 487536.Google ScholarPubMed
Giaschi, D., Douglas, R., Marlin, S. & Cynader, M. (1993). The time course of direction-selective adaptation in simple and complex cells in cat striate cortex. Journal of Neurophysiology 70, 20242034.CrossRefGoogle ScholarPubMed
Greenlee, M.W., Georgeson, M.A., Magnussen, S. & Harris, J.P. (1991). The time course of adaptation to spatial contrast. Vision Research 31, 223236.CrossRefGoogle ScholarPubMed
Hammond, P., Mouate, G.S. & Smith, A.T. (1985). Motion aftereffects in cat striate cortex elicited by moving gratings. Experimental Brain Research 60, 411416.CrossRefGoogle ScholarPubMed
Hammond, P., Mouate, G.S. & Smith, A.T. (1986). Motion aftereffects in cat siriate cortex elicited by moving texture. Vision Research 26, 10551060.CrossRefGoogle ScholarPubMed
Hochstein, S. & Shapley, R.M. (1976). Quantitative analysis of retinal ganglion cell classifications. Journal of Physiology 262, 237264.CrossRefGoogle ScholarPubMed
Lee, B.B., Creutzfeldt, O.D. & Elepfandt, A. (1979). The responses of magno- and parvocellular cells of the monkey's lateral geniculate body to moving stimuli. Experimental Brain Research 35, 547557.CrossRefGoogle ScholarPubMed
LeVay, S. (1988). Patchy intrinsic projections in visual cortex, area 18 of the cat: Morphological and immunocytochemical evidence for an excitatory function. Journal of Comparative Neurology 269, 265274.CrossRefGoogle ScholarPubMed
Levick, W.R. & Thibos, L.N. (1982). Analysis of orientation bias in cat retina. Journal of Physiology 329, 243261.Google Scholar
Lindstrom, S. & Wrobel, A. (1990). Frequency dependent corticofugal excitation of principal cells in the cat's lateral geniculate nucleus. Experimental Brain Research 79, 313318.CrossRefGoogle Scholar
Maffei, L., Bernardi, N. & Bisti, S. (1986). Interocular transfer of adaptation after-effect in neurons of area 17 and 18 of split chiasm cats. Journal of Neurophysiology 55, 966976.CrossRefGoogle ScholarPubMed
Maffei, L., Fiorentini, A. & Bisti, S. (1973). Neural correlates of perceptual adaptation to gratings. Science 182, 10361039.Google Scholar
Magnussen, S. & Greenlee, M.W. (1985). Marathon adaptation to spatial contrast: Saturation in sight. Vision Research 25, 14091411.Google Scholar
Marlin, S.G., Hasan, S.J. & Cynader, M.S. (1988). Direction-selective adaptation in simple and complex cells in cat striate cortex. Journal of Neurophysiology 59, 13141330.CrossRefGoogle ScholarPubMed
Montero, V.M. (1991). A quantitative study of synaptic contacts on interneurons and relay cells of the cat lateral geniculate nucleus. Experimental Brain Research 86, 257270.CrossRefGoogle ScholarPubMed
Movshon, J.A. & Lennie, P. (1979). Pattern-selective adaptation in visual cortical neurones. Nature 278, 850852.Google Scholar
Movshon, J.A., Chambers, B.E.I. & Blakemore, C. (1972). Intraocular transfer in normal humans and those who lack stereopsis. Perception 1, 483490.Google Scholar
Ohzawa, I., Sclar, G. & Freeman, R. (1985). Contrast gain control in the cat's visual system. Journal of Neurophysiology 54, 651667.CrossRefGoogle ScholarPubMed
Robson, J.G. (1975). Receptive fields: Neural representation of the spatial and intensive attributes of the visual image. In Seeing, Volume 5 of Handbook of Perception, ed. Carterette, E.C. & Friedman, M.S., pp. 81112. New York: Academic Press.Google Scholar
Sclar, G., Ohzawa, I. & Freeman, R.D. (1985). Contrast gain control in the kitten's visual system. Journal of Neurophysiology 54, 668675.Google Scholar
Shapley, R.M. & Enroth-Cugell, C. (1984). Visual adaptation and retinal gain controls. Progress in Retinal Research 3, 263343.CrossRefGoogle Scholar
Shapley, R.M. & Victor, J.D. (1979). The contrast gain control of the cat retina. Vision Research 19, 431434.CrossRefGoogle ScholarPubMed
Shapley, R.M. & Victor, J.D. (1981). How the contrast gain control modifies the frequency responses of cat retinal ganglion cells. Journal of Physiology 318, 161179.CrossRefGoogle ScholarPubMed
Shou, T., Ruan, D. & Zhou, Y. (1986). The orientation bias of LGN neurons shows topographic relation to are centralis in the cat retina. Experimental Brain Research 64, 233236.Google Scholar
Shou, T. & Leventhal, A.G. (1989). Organized arrangement of orientation sensitive relay cells in the cat's dorsal lateral geniculate nucleus. Journal of Neuroscience 9, 42874302.CrossRefGoogle ScholarPubMed
Sillito, A.M., Cudeiro, J. & Murphy, P.C. (1993). Orientation sensitive elements in the corticofugal influence on center-surround interactions in the dorsal lateral geniculate nucleus. Experimental Brain Research 93, 616.CrossRefGoogle Scholar
Sillito, A.M., Jones, H.E., Gerstein, G.L. & West, D.C. (1994). Feature-linked synchronization of thalamic relay cell firing induced by feedback from the visual cortex. Nature 369, 479482.Google Scholar
Smith, A.T. & Hammond, P. (1985). The pattern specificity of velocity aftereffect. Experimental Brain Research 60, 7178.CrossRefGoogle Scholar
IIISmith, E.L., Chino, Y.M., IIIRider, W.H., Kitagawa, K. & Langston, A. (1990). Orientation bias of neurons in the lateral geniculate nucleus of macaque monkeys. Visual Neuroscience 5, 525545.CrossRefGoogle ScholarPubMed
Soodak, R.F., Shapley, R.M. & Kaplan, E. (1987). Linear mechanism of orientation tuning in the retina and lateral geniculate nucleus of the cat. Journal of Neurophysiology 58, 267275.Google Scholar
Stone, J. & Fukuda, Y. (1974). Properties of cat retinal ganglion cells: A comparison of W-cells with X- and Y-cells. Journal of Neurophysiology 24, 722748.CrossRefGoogle Scholar
Thompson, K.G., Zhou, Y. & Leventhal, A.G. (1994 a). Direction sensitive cells within the A laminae of the cat's LGNd. Visual Neuroscience 14, 927938.CrossRefGoogle Scholar
Thompson, K.G., Leventhal, A.G., Zhou, Y. & Liu, D. (1994 b). Stimulus dependence of orientation and direction sensitivity of cat LGNd relay cells without cortical inputs: A comparison with area 17 cells. Visual Neuroscience 14, 939951.Google Scholar
Ts'o, D.Y., Gilbert, C.D. & Wiesel, T.N. (1986). Relationships between horizontal interactions and functional architecture in cat striate cortex as revealed by cross-correlation analysis. Journal of Neuroscience 6, 11601170.CrossRefGoogle ScholarPubMed
Tsumoto, T., Creutzfeldt, O.D. & Legendy, C.R. (1978). Functional organization of the corticofugal system from visual cortex to lateral geniculate nucleus in the cat. Experimental Brain Research 32, 345364.CrossRefGoogle ScholarPubMed
Vautin, R.G. & Berkley, M. (1977). Responses of single cells in cat visual cortex to prolonged stimulus movement: Neural correlates of visual aftereffects. Journal of Neurophysiology 40, 10511065.CrossRefGoogle ScholarPubMed
Vidyasagar, T.R. & Urbas, J.V. (1982). Orientation sensitivity of cat LGNd neurons with and without inputs from visual cortical areas 17 and 18. Experimental Brain Research 46, 157169.Google Scholar
Vidyasagar, T.R. (1990). Pattern adaptation in cat visual cortex is a co-operative phenomenon. Neuroscience 36, 175179.CrossRefGoogle ScholarPubMed
Wolfe, J. & Held, R. (1983). Binocular adaptation that cannot be measured monocularly. Perception 11, 287295.CrossRefGoogle Scholar
Zar, J.H. (1974). Circular distributions. In Biostatistical Analysis, Englewood Cliffs, New Jersey: Prentice-Hall, Inc.Google Scholar
Zhou, Y., Leventhal, A.G. & Thompson, K.G. (1995). Visual deprivation does not affect the orientation and direction sensitivity of relay cells in the dorsal lateral geniculate nucleus of the cat. Journal of Neuroscience 15, 689698.CrossRefGoogle ScholarPubMed