Lateral feedback from monophasic horizontal cells to cones in carp retina. I. Experiments

The spatial and color coding of the monophasic horizontal cells were studied in light- and dark-adapted retinae. Slit displacement experiments revealed differences in integration area for the different cone inputs of the monophasic horizontal cells. The integration area measured with a 670-nm stimulus was larger than that measured with a 570-nm stimulus. Experiments in which the diameter of the test spot was varied, however, revealed at high stimulus intensities a larger summation area for 520-nm stimuli than for 670-nm stimuli. The reverse was found for low stimulus intensities. To investigate whether these differences were due to interaction between the various cone inputs to the monophasic horizontal cell, adaptation experiments were performed. It was found that the various cone inputs were not independent. Finally, some mechanisms for the spatial and color coding will be discussed.

[1]  M. Piccolino,et al.  Sustained feedback effects of L-horizontal cells on turtle cones , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[2]  H Spekreijse,et al.  Receptive Field Organization of the S-Potential , 1968, Science.

[3]  D. A. Burkhardt,et al.  Sensitization and centre‐surround antagonism in Necturus retina , 1974, The Journal of physiology.

[4]  J. Dowling,et al.  Isolated horizontal cells from carp retina demonstrate dopamine-dependent accumulation of cyclic AMP. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[5]  S. Usui,et al.  Discrete nonlinear reduction model for horizontal cell response in the carp retina , 1983, Vision Research.

[6]  A Kaneko,et al.  Quantitative analysis of photoreceptor inputs to external horizontal cells in the goldfish retina. , 1982, The Japanese journal of physiology.

[7]  A Kaneko,et al.  Electrical connexions between horizontal cells in the dogfish retina , 1971, The Journal of physiology.

[8]  M. Piccolino,et al.  Center-surround antagonistic organization in small-field luminosity horizontal cells of turtle retina. , 1981, Journal of neurophysiology.

[9]  A. L. Byzov,et al.  Amplification of graded potentials in horizontal cells of the retina , 1977, Vision Research.

[10]  A Lasansky,et al.  Synaptic action mediating cone responses to annular illumination in the retina of the larval tiger salamander. , 1981, The Journal of physiology.

[11]  H. Spekreijse,et al.  The Dynamic Characteristics of Color-Coded S-Potentials , 1970, The Journal of general physiology.

[12]  W. Stell,et al.  Color‐specific interconnections of cones and horizontal cells in the retina of the goldfish , 1975, The Journal of comparative neurology.

[13]  T. Yagi,et al.  Interaction between the soma and the axon terminal of retinal horizontal cells in Cyprinus carpio. , 1986, The Journal of physiology.

[14]  M. Tachibana,et al.  Membrane properties of solitary horizontal cells isolated from goldfish retina. , 1981, The Journal of physiology.

[15]  T. Lamb,et al.  Spatial properties of horizontal cell responses in the turtle retina. , 1976, The Journal of physiology.

[16]  A Kaneko,et al.  Receptive field organization of bipolar and amacrine cells in the goldfish retina , 1973, The Journal of physiology.

[17]  H. Spekreijse,et al.  The “silent substitution” method in visual research , 1982, Vision Research.

[18]  G. Mitarai Identification of five types of S-potential and their corresponding generating sites in the horizontal cells of the carp retina , 1974 .

[19]  D. Baylor,et al.  Receptive fields of cones in the retina of the turtle , 1971, The Journal of physiology.

[20]  H. Spekreijse,et al.  Lateral feedback from monophasic horizontal cells to cones in carp retina. II. A quantitative model , 1989, The Journal of general physiology.

[21]  H. Spekreijse,et al.  Color fundamentals deduced from carp ganglion cell responses. , 1984, Vision research.

[22]  J. Dowling,et al.  Responsiveness and receptive field size of carp horizontal cells are reduced by prolonged darkness and dopamine. , 1985, Science.

[23]  W. Stell,et al.  Goldfish retina: functional polarization of cone horizontal cell dendrites and synapses , 1975, Science.

[24]  J. Dowling,et al.  Factors affecting release of 3H-dopamine from perfused carp retina , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  A. L. Byzov,et al.  Electrical properties of subsynaptic and nonsynaptic membranes of horizontal cells in fish retina , 1974 .

[26]  H. Wolburg,et al.  Gap junctions between horizontal cells in the cyprinid fish alter rapidly their structure during light and dark adaptation , 1986, Neuroscience Letters.

[27]  Kosuke Watanabe,et al.  Re-examination of horizontal cells in the carp retina with procion yellow electrode , 1976, Vision Research.

[28]  A. Kaneko,et al.  Convergence of signals from red-sensitive and green-sensitive cones onto L-type external horizontal cells of the goldfish retina , 1983, Vision Research.

[29]  K I Naka,et al.  Dogfish ganglion cell discharge resulting from extrinsic polarization of the horizontal cells , 1972, The Journal of physiology.

[30]  Ido Perlman,et al.  Light adaptation in luminosity horizontal cells in the turtle retina Role of cellular coupling , 1984, Vision Research.

[31]  F S Werblin Anomalous rectification in horizontal cells. , 1975, The Journal of physiology.

[32]  A Kaneko,et al.  Membrane properties and the signal conduction of the horizontal cell syncytium of the teleost retina. , 1987, Neuroscience research. Supplement : the official journal of the Japan Neuroscience Society.

[33]  A. Kaneko Physiological and morphological identification of horizontal, bipolar and amacrine cells in goldfish retina , 1970, The Journal of physiology.

[34]  T. Iu Study of synaptic transmission between photoreceptor and horizontal cell by electric stimulations of the retina , 1968 .

[35]  Satoru Kato,et al.  Dopamine modulates S-potential amplitude and dye-coupling between external horizontal cells in carp retina , 1983, Nature.

[36]  K. Negishi,et al.  A GABA antagonist, bicuculline, exerts its uncoupling action on external horizontal cells through dopamine cells in carp retina , 1983, Neuroscience Letters.

[37]  A. Kaneko,et al.  Coupling between horizontal cells in the carp retina revealed by diffusion of lucifer yellow , 1984, Neuroscience Letters.

[38]  A. Kaneko,et al.  Depolarizing responses of L-type external horizontal cells in the goldfish retina under intense chromatic background , 1984, Vision Research.

[39]  K. Negishi,et al.  Regulatory effect of dopamine on spatial properties of horizontal cells in carp retina , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[40]  A. L. Byzov,et al.  Ionic mechanisms underlying the nonlinearity of horizontal cell membrane , 1981, Vision Research.

[41]  J. Scholes Colour receptors, and their synaptic connexions, in the retina of a cyprinid fish. , 1975, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[42]  I. Perlman,et al.  Light adaptation of red cones and L1-horizontal cells in the turtle retina: effect of the background spatial pattern , 1987, Vision Research.