Hostname: page-component-78c5997874-fbnjt Total loading time: 0 Render date: 2024-11-10T10:56:37.114Z Has data issue: false hasContentIssue false

Modulation of endogenous dopamine release in the fish retina by light and prolonged darkness

Published online by Cambridge University Press:  02 June 2009

Reto Weiler
Affiliation:
The Marine Biological Laboratory, Woods Hole
William H. Baldridge
Affiliation:
The Marine Biological Laboratory, Woods Hole
Stuart C. Mangel
Affiliation:
The Marine Biological Laboratory, Woods Hole
John E. Dowling
Affiliation:
The Marine Biological Laboratory, Woods Hole

Abstract

The effect of light stimuli and prolonged darkness on the release of endogenous dopamine was measured in the white perch and hybrid bass retinas. Isolated retinas were superfused and released dopamine was measured using extraction and high-pressure liquid chromatography separation techniques. Potassium-induced release did not depend on the background illumination nor on the period of previous darkness. Steady white light did not affect release, but flickering light of 2 Hz increased release about two-fold. During prolonged darkness, the release of dopamine increased steadily over the test period of 2 h, but only if the experiments were performed at night. During the day such an increase was not observed. The increased release during prolonged darkness at night was turned off by a short period of steady white light. The release patterns obtained from the white perch and the hybrid bass were similar. However, the hybrid bass retina showed much lower levels of dopamine than did the white perch retina.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Baldridge, W.H. & Ball, A.K. (1991). Background illumination reduces horizontal cell receptive-field size in both, normal and 6-hydroxydopamine-lesioned goldfish retinas. Visual Neuroscience 7, 441450.CrossRefGoogle ScholarPubMed
BaldridGe, W.H., Weiler, R. & Dowling, J.E. (1995). Dark-suppression and light-sensitization of horizontal cell responses in the hybrid bass retina. Visual Neuroscience 12, 611620.CrossRefGoogle ScholarPubMed
Bauer, B., Ehinger, B. & Aberg, L. (1980). [3H]-Dopamine release from the rabbit retina. Albrecht von Graefes Archiv der Klinischen Ophthalmologic 215, 7986.Google ScholarPubMed
Boatright, J.H., Hoel, M.J. & Ivuone, P.M. (1989). Stimulation of endogenous dopamine release and metabolism in amphibian retina by light- and K+-evoked depolarization. Brain Research 482, 164168.CrossRefGoogle ScholarPubMed
Brainard, G.C. & Morgan, W.W. (1987). Light-induced stimulation of retinal dopamine: A dose-response relationship. Brain Research 424, 199203.CrossRefGoogle ScholarPubMed
Cahill, G.M. & Besharse, J.C. (1993). Circadian clock functions localized in Xenopus retinal photoreceptors. Neuron 10, 573577.CrossRefGoogle ScholarPubMed
Cohen, J.L. & Dowling, J.E. (1983). The role of the retinal interplexiform cell: Effects of 6-hydroxydopamine on the spatial properties of carp horizontal cells. Brain Research 264, 307310.CrossRefGoogle ScholarPubMed
Dearry, A. & Burnside, B. (1985). Dopamine inhibits forskolin- and IBMX- induced dark-adaptive retinomotor movements in isolated teleost retinas. Journal of Neurochemistry 44, 17531763.CrossRefGoogle ScholarPubMed
Dearry, A. & Burnside, B. (1989). Light-induced dopamine release from eleost retinas acts as a light-adaptive signal to the retinal pigment epithelium. Journal of Neurochemistry 53, 870878.CrossRefGoogle Scholar
Djamgoz, M.B.A. & Wagner, H.-J. (1992). Localization and function of dopamine in the adult vertebrate retina. Neurochemistry International 20, 139191.CrossRefGoogle ScholarPubMed
Dowling, J.E. (1987). The Retina. Cambridge, Massachusetts and London, England: The Belknap Press of Harvard University Press.Google Scholar
Dowling, J.E. & Ehinger, B. (1978). Synaptic organization of the dopaminergic neurons in the rabbit retina. Journal of Comparative Neurology 180, 203220.CrossRefGoogle ScholarPubMed
Ehinger, B. & Floren, I. (1976). Indoleamine-accumulating neurons in the retina of rabbit, cat and goldfish. Cell and Tissue Research 175, 3749.CrossRefGoogle Scholar
Godley, B.F. & Wurtman, R.J. (1988). Release of endogenous dopamine from the superfused rabbit retina in vitro: Effect of light stimulation. Brain Research 452, 393395.CrossRefGoogle ScholarPubMed
Green, C.B., Cahill, G.M. & Besharse, J.C. (1995). Regulation of tryptophan hydroxylase expression by a retinal circadian oscillator in vito. Brain Research 677, 283290.CrossRefGoogle Scholar
Hamasaki, D.I., Trattler, W.B. & Hajek, A.S. (1986). Light ON depresses and light OFF enhances the release of dopamine from the cat's retina. Neuroscience Letters 68, 112116.CrossRefGoogle ScholarPubMed
Hedden, W.L. & Dowling, J.E. (1978). The interplexiform cell system II. Effects of dopamine on goldfish retinal neurons. Proceedings of the Royal Society (London) 201, 407412.Google Scholar
Kirsch, M. & Wagner, H.-J. (1989). Release pattern of endogenous dopamine in teleost retinas during light adaptation and pharmacological stimulation. Vision Research 29, 147154.CrossRefGoogle ScholarPubMed
Knapp, A.G. & Dowling, J.E. (1987). Dopamine enhances excitatory amino acid-gated conductances in cultured retinal horizontal cells. Nature 325, 437438.CrossRefGoogle ScholarPubMed
Kolbinger, W., Kohler, K., Oetting, H. & Weiler, R. (1990). Endogenous dopamine and cyclic events in the fish retina. I. HPLC assay of total content, release and metabolic turnover during different light/dark cycles. Visual Neuroscience 5, 143149.CrossRefGoogle ScholarPubMed
Kolbinger, W. & Weiler, R. (1993). Modulation of endogenous dopamine release in the turtle retina: Effects of light, calcium, and neurotransmitters. Visual Neuroscience 10, 10351041.CrossRefGoogle ScholarPubMed
Kramer, S.G. (1971). Dopamine: A retinal neurotransmitter. I. Retinal uptake, storage and light stimulated release of 3H-dopamine in vivo. Investigative Ophthalmology and Visual Science 10, 438452.Google Scholar
Lin, Z.-S. & Yazulla, S. (1994). Depletion of retinal dopamine increases brightness perception in goldfish. Visual Neuroscience 11, 683693.CrossRefGoogle ScholarPubMed
Mangel, S.C., Baldridge, W.H., Weiler, R. & Dowling, J.E. (1994). Threshold and chromatic sensitivity changes in fish cone horizontal cells following prolonged darkness. Brain Research 659, 5561.CrossRefGoogle ScholarPubMed
Mangel, S.C. & Dowling, J.E. (1985). Responsiveness and receptive field size of carp horizontal cells are reduced by prolonged darkness and dopamine. Science 229, 11071109.CrossRefGoogle ScholarPubMed
Mangel, S.C. & Dowling, J.E. (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, 91121.Google ScholarPubMed
Mangel, S. C. & Wang, Y. (1995). Dopamine acts as a circadian clock effector by activating D4 receptors in the fish retina. Neuroscience Abstracts 21, 903.Google Scholar
Mora-Ferrer, C. & Neumeyer, C. (1993). Reduced red-green discrimination in goldfish after application of dopamine antagonists. Investigative Ophthalmology and Visual Science (Suppl.) 34, 752.Google Scholar
Negishi, K. & Drujan, B.D. (1979). Effects of catecholamines and related compounds on horizontal cells in the fish retina. Journal of Neuroscience Research 4, 311334.CrossRefGoogle ScholarPubMed
Pierce, M.E. & Besharse, J.C. (1985). Circadian regulation of retinomotor movements I. Interaction of melatonin and dopamine in the control of cone length. Journal of General Physiology 86, 671689.CrossRefGoogle ScholarPubMed
Pierce, M.E. & Besharse, J.C. (1988). Circadian regulations of retinomotor movements II. The role of GABA in the regulation of cone position. Journal of Comparative Neurology 270, 279287.CrossRefGoogle ScholarPubMed
Reading, H.W. (1983). Dopaminergic receptors in bovine retina and their interactions with thyrotropin-releasing hormone. Journal of Neurochemistry 41, 15871595.CrossRefGoogle ScholarPubMed
Teranishi, T., Negishi, K. & Kato, S. (1983). Dopamine modulates S-Potential amphitude and dye-coupling between external horizontal cells in carp retina. Nature 301, 243246.CrossRefGoogle ScholarPubMed
Tornqvist, K., Yang, X.-L. & Dowling, J.E. (1988). Modulation of cone horizontal cell activity in the teleost fish retina. III. Effects of prolonged darkness and dopamine on electrical coupling between horizontal cells. Journal of Neuroscience 8, 22792288.CrossRefGoogle ScholarPubMed
Umino, O., Lee, Y. & Dowling, J.E. (1991). Effects of light stimuli on the release of dopamine from interplexiform cells in the white perch retina. Visual Neuroscience 7, 451458.CrossRefGoogle ScholarPubMed
Wang, Y. & Mangel, S.C. (1996). A circadian clock regulates rod and cone input to fish retinal cone horizontal cells. Proceedings of the National Academy of Sciences of the U.S.A. 93, 46554660.CrossRefGoogle ScholarPubMed
Weiler, R., Kohler, K., Kirsch, M. & Wagner, H.-J. (1988 a). Glutamate and dopamine modulate synaptic plasticity in horizontal cell dendrites of fish retina. Neuroscience Letters 87, 205209.CrossRefGoogle ScholarPubMed
Weiler, R., Kohler, K., Kolbinger, W., Wolburg, H., Kurz-Isler, G. & Wagner, H.-J. (1988 b). Dopaminergic neuromodulation in the retinas of lower vertebrates. Neuroscience Research Supplement 8, S183–S196.CrossRefGoogle ScholarPubMed
Weiler, R., Kolbinger, W. & Kohler, K. (1989). Reduced light responsiveness of the cone pathway during prolonged darkness does not result from an increase of dopaminergic activity in the fish retina. Neuroscience Letters 99, 214218.CrossRefGoogle Scholar
Weiler, R. & Akopian, A. (1992). Effects of background illuminations on the receptive-field size of horizontal cells in the turtle retina are mediated by dopamine. Neuroscience Letters 140, 121124.CrossRefGoogle ScholarPubMed
Witkovsky, P. & Dearry, A. (1993). Functional roles of dopamine in the vertebrate retina. In Retinal Research, ed. Osborne, N.N. & Chader, G.J., pp. 248280. Oxford: Pergamon Press.Google Scholar
Yang, X.-L., Tornqvist, K. & Dowling, J.E. (1988). Modulation of cone horizontal cell activity in the teleost fish retina. I. Effects of prolonged darkness and background illumination on light responsiveness. Journal of Neuroscience 8, 22592268.CrossRefGoogle ScholarPubMed
Yang, X.-L., Fan, T.-X. & Shen, W. (1994). Effects of prolonged darkness on light responsiveness and spectral sensitivity of cone horizontal cells in carp retina in vivo. Journal of Neuroscience 14, 326334.CrossRefGoogle ScholarPubMed