TTX attenuates surround inhibition in rabbit retinal ganglion cells

Visual Neuroscience

Volumn 16, Issue 2, 1999, Pages 285-290

  Taylor, W Rowland ^a,b  

^a MAX PLANCK INSTITUTE FOR BRAIN RESEARCH   (Germany)

^b Biology and Environment   (Australia)

Author keywords

Center surround; Electrophysiology; Light responses; Rabbit retina; Recepti ve field properties; Tetrodotoxin

Indexed keywords

SODIUM CHANNEL; TETRODOTOXIN;

ACTION POTENTIAL; ANIMAL; ARTICLE; DARK ADAPTATION; DRUG EFFECT; ELECTROPHYSIOLOGY; PATCH CLAMP; PHOTORECEPTOR; PHOTOSTIMULATION; PHYSIOLOGY; RABBIT; RETINA GANGLION CELL;

ACTION POTENTIALS; ANIMALS; DARK ADAPTATION; ELECTROPHYSIOLOGY; PATCH-CLAMP TECHNIQUES; PHOTIC STIMULATION; PHOTORECEPTORS, VERTEBRATE; RABBITS; RETINAL GANGLION CELLS; SODIUM CHANNELS; TETRODOTOXIN;

EID: 0033103960     PISSN: 09525238     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0952523899162096     Document Type: Article

References (48)

1. AMES, A.I. & NESBETT, F.B. (1981). In vitro retina as an experimental model of the central nervous system. Journal of Neurochemistry 37, 867-877.
2. AMMERMÜLLER, J. & WEILER, R. (1988). Physiological and morphological characterization of OFF-center amacrine cells in the turtle retina. Journal of Comparative Neurology 273, 137-148.
3. BARNES, S. & WERBLIN, F. (1986). Gated currents generate single spike activity in amacrine cells of the tiger salamander. Proceedings of the National Academy of Sciences of the U.S.A. 83, 1509-1512.
4. BELGUM, J.H. & COPENHAGEN, D.R. (1988). Synaptic transfer of rod signals to horizontal and bipolar cells in the retina of the toad (Bufo marinus). Journal of Physiology 396, 225-245.
5. BLOOMFIELD, S. (1996). Effect of spike blockade on the receptive-field size of amacrine and ganglion cells in the rabbit retina. Journal of Neurophysiology 75, 1878-1893.
6. BLOOMFIELD, S.A. (1992). Relationship between receptive field and dendritic field size of amacrine cells in the rabbit retina. Journal of Neurophysiology 68, 711-725.
7. BOYCOTT, B., DOWLING, J., FISHER, S., KOLB, H. & LATIES, A. (1975). Interplexiform cells of the mammalian retina and their comparison with catecholamine-containing retinal cells. Proceedings of the Royal Society B (London) 191, 353-368.
8. BURKHARDT, D.A. (1977). Responses and receptive-field organization of cones in perch retinas. Journal of Neurophysiology 40, 53-62.
9. CALDWELL, J. & DAW, N. (1978). Effects of picrotoxin and strychnine on rabbit retinal ganglion cells: Changes in center surround receptive fields. Journal of Physiology 276, 299-310.
10. COOK, P., LUKASIEWICZ, P. & MCREYNOLDS, J. (1998). Action potentials are required for the lateral transmission of glycinergic transient inhibition in the amphibian retina. Journal of Neuroscience 18, 2301-2308.
11. COOK, P. & WERBLIN, F. (1994). Spike initiation and propagation in wide field transient amacrine cells of the salamander retina. Journal of Neuroscience 14, 3852-3861.
12. DJAMGOZ, M. & WAGNER, H. (1992). Localization and function of dopamine in the adult vertebrate retina. Neurochemistry International 20, 139-191.
13. ENROTH-CUGELL, C. & ROBSON, J.G. (1966). The contrast sensitivity of retinal ganglion cells of the cat. Journal of Physiology 187, 517-552.
14. GOLARD, A., WITKOVSKY, P. & TRANCHINA, D. (1992). Membrane currents of horizontal cells isolated from turtle retina. Journal of Neurophysiology 68, 351-361.
15. GUSTINCICH, S., FEIGENSPAN, A., WU, D., KOOPMAN, L. & RAVIOLA, E. (1997). Control of dopamine release in the retina: A transgenic approach to neural networks. Neuron 18, 723-736.
16. KIRBY, A. (1979). The effect of strychnine, bicuculline, and picrotoxin on X and Y cells in the cat retina. Journal of General Physiology 74, 71-84.
17. KOLB, H. & WEST, R. (1977). Synaptic connections of the interplexiform cell in the retina of the cat. Journal of Neurocytology 6, 155-170.
18. KUFFLER, S.W. (1953). Discharge patterns and functional organization of mammalian retina. Journal of Neurophysiology 16, 37-68.
19. LEVICK, W. (1967). Receptive fields and trigger features of ganglion cells in the visual streak of the rabbits retina. Journal of Physiology 188, 285-307.
20. LINBERG, K. & FISHER, S. (1986). An ultrastructural study of interplexiform cell synapses in the human retina. Journal of Comparative Neurology 243, 561-576.
21. LÖHRKE, S. & HOFMANN, H. (1994). Voltage-gated currents of rabbit A- and B-type horizontal cells in retinal monolayer cultures. Visual Neuroscience 11, 369-378.
22. MAGUIRE, G., LUKASIEWICZ, P. & WERBLIN, F. (1990). Synaptic and voltage-gated currents in interplexiform cells of the tiger salamander retina. Journal of General Physiology 95, 755-770.
23. MANGEL, S. (1991). Analysis of the horizontal cell contribution to the receptive field surround of ganglion cells in the rabbit retina. Journal of Physiology 442, 211-234.
24. MANGEL, S. & DOWLING, J. (1987). The interplexiform-horizontal cell system of the fish retina: Effects of dopamine, light stimulation and time in the dark. Proceedings of the Royal Society B (London) 231, 91-121.
25. MILLER, R. & DACHEUX, R. (1976). Dendritic and somatic spikes in mud-puppy amacrine cells: Identification and TTX sensitivity. Brain Research 104, 157-162.
26. MURAKAMI, M. & TAKAHASHI, K. (1987). Calcium action potential and its use for measurement of reversal potentials of horizontal cell responses in carp retina. Journal of Physiology 386, 165-180.
27. NAKA, K.I. & WITKOVSKY, P. (1972). Dogfish ganglion cell discharge resulting from extrinsic polarization of the horizontal cells. Journal of Physiology 223, 449-460.
28. NGUYEN-LEGROS, J., VERSAUX-BOTTERI, C. & SAVY, C. (1997). Dopaminergic and GABAergic retinal cell populations in mammals. Microscopy Research and Technique 36, 26-42.
29. OYSTER, C. & TAKAHASHI, E. (1977). Interplexiform cells in rabbit retina. Proceedings of the Royal Society B (London) 197, 477-484.
30. PICCOLINO, M., WITKOVSKY, P. & TRIMARCHI, C. (1987). Dopaminergic mechanisms underlying the reduction of electrical coupling between horizontal cells of the turtle retina induced by d-amphetamine, bicuculline, and veratridine. Journal of Neuroscience 7, 2273-2284.
31. RODIECK, R. (1965). Quantitative analysis of cat retinal ganglion cell responses to visual stimuli. Vision Research 5, 601.
32. SAITO, H. (1983). Pharmacological and morphological differences between X- and Y-type ganglion cells in the cat's retina. Vision Research 23, 1299-1308.
33. SANDELL, J. & MASLAND, R. (1989). Shape and distribution of an unusual retinal neuron. Journal of Comparative Neurology 280, 489-497.
34. SMITH, R. & STERLING, P. (1990). Cone receptive field in cat retina computed from microcircuitry. Visual Neuroscience 5, 453-461.
35. SRINIVASAN, M.V., LAUGHLIN, S.B. & DUBS, A. (1982). Predictive coding: a fresh view of inhibition in the retina. Proceedings of the Royal Society B (London) 216, 427-459.
36. STAFFORD, D. & DACEY, D. (1997). Physiology of the Al amacrine: A spiking, axon-bearing interneuron of the macaque monkey retina. Visual Neuroscience 14, 507-522.
37. STONE, J. & HOFFMANN, K. (1972). Very slow-conducting ganglion cells in the cat's retina: A major, new functional type? Brain Research 43, 610-616.
38. TAYLOR, W.R. (1996). Response properties of long-range axon-bearing amacrine cells in the dark-adapted rabbit retina. Visual Neuroscience 13, 599-604.
39. TAYLOR, W.R. & WÄSSLE, H. (1995). Receptive field properties of starburst cholinergic amacrine cells in the rabbit retina. European Journal of Neuroscience 7, 2308-2321.
40. THIBOS, L.N. & WERBLIN, F.S. (1978). The properties of surround antagonism elicited by spinning windmill patterns in the mudpuppy retina. Journal of Physiology 278, 101-116.
41. TOYODA, J. & TONOSAKI, K. (1978). Effect of polarisation of horizontal cells on the on-center bipolar cell of carp retina. Nature 276, 399-400.
42. UEDA, Y., KANEKO, A. & KANEDA, M. (1992). Voltage-dependent ionic currents in solitary horizontal cells isolated from cat retina. Journal of Neurophysiohgy 68, 1143-1150.
43. VANEY, D. (1980). A quantitative comparison between the ganglion cell populations and axonal outflows of the visual streak and periphery of the rabbit retina. Journal of Comparative Neurology 189, 215-233.
44. VANEY, D., LEVICK, W. & THIBOS, L. (1981). Rabbit retinal ganglion cells. Receptive field classification and axonal conduction properties. Experimental Brain Research 44, 27-33.
45. VANEY, D.I. (1990). The mosaic of amacrine cells in the mammalian retina. In Progress in Retinal Research, ed. OSBORNE, N. & CHADER, J. pp. 49-100. Oxford: Pergamon Press.
46. + action potentials in the dendrites of mammalian retinal ganglion cells. Society for Neuroscience Abstract 23, 1961.
47. WERBLIN, F.S. (1974). Control of retinal sensitivity. II. Lateral interactions at the outer plexiform layer. Journal of General Physiology 63, 62-87.
48. WERBLIN, F.S. & COPENHAGEN, D.R. (1974). Control of retinal sensitivity. III. Lateral interactions at the innerplexiform layer. Journal of General Physiology 63, 88-110.