Dopaminergic modulation and rod contribution in the generation of oscillatory potentials in the tiger salamander retina

Vision Research

Volumn 47, Issue 3, 2007, Pages 309-314

  Perry, B ^a,b   George, J S ^a  

^a LOS ALAMOS NATIONAL LABORATORY   (United States)

^b UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER   (United States)

Author keywords

Adaptation; Dopamine; Oscillatory potentials; Rod cone pathway; Tiger salamander

Indexed keywords

2,3,4,5 TETRAHYDRO 7,8 DIHYDROXY 1 PHENYL 1H 3 BENZAZEPINE; DOPAMINE 2 RECEPTOR; QUINPIROLE; SULPIRIDE;

ARTICLE; CONTROLLED STUDY; DOPAMINERGIC ACTIVITY; LIGHT ADAPTATION; NIGHT VISION; NONHUMAN; OSCILLATION; OSCILLATORY POTENTIAL; PRIORITY JOURNAL; RETINA ROD; SALAMANDER; STIMULUS; TIGER;

ADAPTATION, PHYSIOLOGICAL; AMBYSTOMA; ANIMALS; BIOLOGICAL CLOCKS; CONES (RETINA); ELECTRORETINOGRAPHY; PHOTIC STIMULATION; RECEPTORS, DOPAMINE; RECEPTORS, DOPAMINE D1; RECEPTORS, DOPAMINE D2; RETINA; RODS (RETINA);

EID: 33846222829     PISSN: 00426989     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.visres.2006.11.004     Document Type: Article

References (53)

1. Abeles M. Role of cortical neuron: integrator or coincidence detector?. Israeli Journal of Medical Science 18 (1982) 83-92
2. Aguilar M., and Stiles W.S. Saturation of the rod mechanism of the retina at high levels of saturation. Optica Acta 1 (1954) 59-65
3. Akopian A., and Witkovsky P. D2 dopamine receptor-mediated inhibition of hyperpolarization-activated current in rod photoreceptors. Journal of Neurophysiology 76 (1996) 1828-1835
4. Alcayaga J., Bustamante S., and Gutierrez O.C. Fast activity and oscillatory potential of carp retina in the frequency domain. Vision Research 29 (1989) 949-955
5. Algvere P., and Wachtmeister L. On the oscillatory potentials of the human electroretinogram in light and dark adaptation. II. Effect of adaptation to background light and subsequent recovery in the dark. A Fourier analysis. Acta Ophthalmologica 50 (1972) 827-862
6. Algvere P., and Westbeck S. Human ERG in response to flashes of light during the course of dark adaptation: a Fourier analysis of the oscillatory potentials. Vision Research 12 (1972) 195-214
7. Alonso J.M., Usrey W.M., and Reid R.C. Precisely correlated firing in cells of the lateral geniculate nucleus. Nature 383 (1996) 815-819
8. Brindley G.S. Responses to illumination recorded by microelectrodes from the frogs retina. Journal of Physiology - London 134 (1956) 360-384
9. Cobb W., and Morton H.B. The human electroretinogram with special reference to responses to high intensity flashes. Electroencephalography in Clinical Neurophysiology 5 (1953) 622
10. Coupland S.G. Oscillatory potential changes related to stimulus intensity and light adaptation. Documenta Ophthalmologica 66 (1987) 195-205
11. DeVries S.H., and Schwartz E.A. Modulation of an electrical synapse between pairs of catfish horizontal cells by dopamine and second messengers. Journal of Physiology 414 (1989) 351-375
12. Dong C.J., Agey P., and Hare W.A. Origins of the electroretinogram oscillatory potentials in the rabbit retina. Visual Neuroscience 21 (2004) 533-543
13. el Azazi M., Wang L., Eklund A., and Wachtmeister L. Background light adaptation of the retinal neuronal adaptive system. II. Dynamic effects. Documenta Ophthalmologica 109 (2004) 201-213
14. K(V)) in retinal bipolar cells by ascorbate is mediated by dopamine D1 receptors. Visual Neuroscience 16 (1999) 923-931
15. Fatechand R. Rod and cone generation of wavelets in the frog electroretinogram. Vision Research 18 (1978) 224-232
16. Granit R.L., and Munsterhjelm A. The electrical response of dark adapted frog's eye to monochromatic stimuli. Journal of Physiology 88 (1937) 436-458
17. Gutierrez O., and Spiguel R.D. Oscillatory potentials of the cat retina effects of adrenergic drugs. Life Sciences 13 (1973) 991-999
18. Heckenlively J.R., Martin D.A., and Rosenbaum A.L. Loss of electroretinographic oscillatory potentials, optic atrophy and dysplasia in congenital stationary blindness. American Journal of Ophthalmology 96 (1983) 526-534
19. Hempel F.G. Modification of the rabbit electroretinogram by reserpine. Ophthalmology Research 4 (1972/1973) 65-67
20. Henkes H.E., and Houtsmüller A.J. Fundus diabeticus. An evaluation of the prediabetic stage. American Journal of Ophthalmology 60 (1965) 662-670
21. Hood D.C., and Finkelstein M.A. (1986), Wiley, New York
22. Ishikane H., Gangi M., Honda S., and Tachibana M. Synchronized retinal oscillations encode essential information for escape behavior in frogs. Nature Neuroscience 8 (2005) 1087-1095
23. King-Smith P.E., Loffing D.H., and Jones R. Rod and cone ERGs and their oscillatory potentials. Investigative Ophthalmology and Visual Science 27 (1986) 270-273
24. Knapp A.G., and Dowling J.E. Dopamine enhances excitatory amino acid-gated conductances in cultured retinal horizontal cells. Nature 325 (1987) 437-439
25. Konig P., Engel A.K., and Singer W. Integrator or coincidence detector? The role of the cortical neuron revisited. Trends in Neuroscience 19 (1996) 130-137
26. Korol S., Leuenberger P.M., Englert U., and Babel J. In vivo effects of glycine on retinal ultrastructure and averaged electroretinogram. Brain Research 97 (1975) 235-251
27. Krizaj D., Gabriel R., Owen W.G., and Witkovsky P. Dopamine D2 receptor-mediated modulation of rod-cone coupling in the Xenopus retina. Journal of Comparative Neurology 398 (1998) 529-538
28. Krizaj D., and Witkovsky P. Effects of submicromolar concentrations of dopamine on photoreceptor to horizontal cell communication. Brain Research 627 (1993) 122-128
29. Lachapelle P. Evidence for intensity-coding oscillatory potential in the human electroretinogram. Vision Research 31 (1991) 767-774
30. Lachapelle P., Little J.M., and Polomeno R.C. The photopic electroretinogram in congenital stationary night blindness with myopia. Investigative Ophthalmology and Visual Science 24 (1983) 442-450
31. Li X.-X., Yuan N., Hong J., and Song P. The influence of adaptation on the oscillatory potentials of the human electroretinogram. Documenta Ophthalmologica 76 (1991) 389-394
32. Liu Y., and Lasater E.M. Calcium currents in turtle retinal ganglion cells. II dopamine modulation via a cyclic AMP-dependent mechanism. Journal of Neurophysiology 71 (1994) 743-752
33. Molotchnikoff S., Shumikhina S., and Moisan L.E. Stimulus-dependent oscillations in the cat visual cortex: differences between bar and grating stimuli. Brain Research 731 (1996) 91-100
34. Müller W., Gauss J., Spittel U., and Dück K.-H. Oscillatory potentials in cases of systemic hypertension. Documenta Ophthalmologica 40 (1984) 167-171
35. Muresan Z., and Besharse J.C. D2-like dopamine receptors in amphibian retina: Localization with fluorescent ligands. Journal of Comparative Neurology 331 (1993) 149-160
36. Ogden T.E., and Wylie R. Avian retina. I. Microelectrode depth and marking studies of local ERG. Journal of Neurophysiology 34 (1971) 357-361
37. Pfeiffer-Linn C.L., and Lasater E.M. Multiple second-messenger system modulation of voltage-activated calcium currents in teleost retinal horizontal cells. Journal of Neurophysiology 71 (1998) 743-752
38. Rector D.M., and George J.S. Continuous image and electrophysiological recording with real time processing and control. Methods 25 (2001) 151-163
39. Sherry D.M., Bui D.D., and Degrip W.J. Identification and distribution of photoreceptor subtypes in the neotenic tiger salamander retina. Visual Neuroscience 15 (1998) 1175-1187
40. Simonsen S.E. Electroretinography study of diabetics. A preliminary report. Acta Ophthalmologica (Copenhagen) 43 (1965) 841-843
41. Stella S.L., and Thoreson W.B. Differential modulation of rod and cone calcium currents in tiger salamander retina by D2 dopamine receptors and cAMP. European Journal of Neuroscience 12 (2000) 3537-3548
42. Usami E. Studies on ERG of occlusion of the retinal artery and vein especially on the prognostic value. Nippon Ganka Gakkai Zasshi 71 (1967) 39-45
43. Wachtmeister L. On the oscillatory potentials of the electroretinogram in light and dark adaptation. Acta Ophthalmologica 50 (1972) 1-30
44. Wachtmeister L. On the oscillatory potentials of the human electroretinogram in light and dark adaptation. Part 3, Thresholds and relation to stimulus intensity on adaptation to background light. Acta Ophthalmologica 51 (1973) 95-113
45. Wachtmeister L. Further studies of the chemical sensitivity of the oscillatory potentials of the electroretinogram (ERG). I. GABA- and glycine antagonists. Acta Ophthalmologica 58 (1980) 712-725
46. Wachtmeister L. Further studies of the chemical sensitivity of the oscillatory potentials of the electroretinogram (ERG). II. Glutamate- aspartate- and dopamine antagonists. Acta Ophthalmologica 59 (1981) 247-258
47. Wachtmeister L., and Dowling J.E. The oscillatory potentials of the mudpuppy retina. Investigative Ophthalmology and Visual Science 17 (1978) 1176-1188
48. Wachtmeister L., and Hahn I. Spatial properties of the oscillatory potentials of the frog electroretinogram in relation to state of adaptation. Acta Ophthalmologica 65 (1987) 724-730
49. Wang L., el Azazi M., Eklund A., and Wachtmeister L. Background light adaptation of the retinal neuronal adaptive system. Documenta Ophthalmologica 103 (2001) 13-26
50. Witkovsky P. Dopamine and retinal function. Documenta Ophthalmologica 108 (2004) 17-40
51. Wu S.M., and Yang X.L. Electrical coupling between rods and cones in the tiger salamander retina. Proceedings of the National Academy Science 85 (1988) 275-278
52. Yang X.L., and Wu S.M. Modulation of rod-cone coupling by light. Science 244 (1989) 352-354
53. Yang X.L., and Wu S.M. Signal transmission from cones to amacrine cells in dark- and light-adapted tiger salamander retina. Brain Research 1029 (2004) 155-161