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Endogenous dopamine and cyclic events in the fish retina, I: HPLC assay of total content, release, and metabolic turnover during different light/dark cycles

Published online by Cambridge University Press:  02 June 2009

Walter Kolbinger
Affiliation:
Department of Neurobiology, University of Oldenburg, Federal Republic of Germany
Konrad Kohler
Affiliation:
Department of Neurobiology, University of Oldenburg, Federal Republic of Germany
Heike Oetting
Affiliation:
Department of Neurobiology, University of Oldenburg, Federal Republic of Germany
Reto Weiler
Affiliation:
Department of Neurobiology, University of Oldenburg, Federal Republic of Germany

Abstract

In this study, we investigated the potency of dopamine for being an intrinsic signal for cyclic events in the fish retina. Dopaminergic activity was measured during different light/dark cycles, during continuous darkness, and during short-term light and dark adaptation within 1 h. During a 12-h light/12-h dark cycle, the total content of endogenous dopamine was high during the dark phase and low during the light phase. The potassium-induced release of endogenous dopamine followed a parallel time course. The concentration of the dopamine breakdown product 3,4-dihydroxyphenylacetic acid (DOPAC), which reflects the endogenous dopaminergic activity, was high during the light phase and low during the dark phase. Similar alterations occurred in accelerated 6-h light/6-h dark cycles, again indicating a strong coupling of dopaminergic activity with light. The cyclic alterations in the total endogenous dopamine content persisted during continuous darkness after an entrainment of the fish to a 12-h light/12-h dark cycle. Although the magnitude of the change was weaker, changes in dopamine content, potassium-induced dopamine release, and DOPAC were also measured during 1 h of light or dark adaptation. During a 1-h period of dark adaptation, the total content of dopamine and the potassium-induced release of endogenous dopamine increased, while DOPAC values decreased. These values changed in the opposite direction during 1 h of light adaptation.

Our findings strongly suggest that dopamine is the intrinsic signal for light during both the light and dark phases and during short-term adaptation. Light seems to be the major trigger for dopaminergic activity within the fish retina. An endogenous clock might participate in the control of the dopaminergic activity. This has to be, however, confirmed by further investigations.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1990

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References

Arey, L.B. (1915). The occurrence and significance of photomechanical changes in the vertebrate retina–an historical survey. Journal of Comparative Neurology 25, 535554.CrossRefGoogle Scholar
Baldridge, W.H., Ball, A.K. & Miller, R.G. (1987). Dopaminergic regulation of horizontal cell gap junction particle density in goldfish retina. Journal of Comparative Neurology 265, 428436.CrossRefGoogle ScholarPubMed
Bassi, C.J. & Powers, M.K. (1987). Circadian rhythm in goldfish visual sensitivity. Investigative Ophthalmology and Visual Science 28,18111815.Google ScholarPubMed
Boatright, J.H., Hoel, M.J. & Iuvone, 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
Cohen, J., Hadjiconstantinou, M. & Neff, N.H. (1983). Activation of dopamine-containing amacrine cells of the retina: light-induced increase of acidic dopamine metabolites. Brain Research 260,125127.CrossRefGoogle ScholarPubMed
Dearry, A. & Burnside, B. (1986). Dopaminergic regulation of cone retinomotor movement in isolated teleost retinas, I: Induction of cone contraction is mediated by D2 receptors. Journal of Neurochemistry 46, 10061026.CrossRefGoogle ScholarPubMed
Dearry, A. & Burnside, B. (1989). Light-induced dopamine release from teleost retinas acts as a light-adaptive signal to the retinal pigment epithelium. Journal of Neurochemistry 53, 870878.CrossRefGoogle Scholar
Di Paolo, T., Harnois, C. & Daigle, M. (1987). Assay of dopamine and its metabolites in human and rat retina. Neuroscience Letters 74, 250254.CrossRefGoogle ScholarPubMed
Dowling, J.E. & Ehinger, B. (1978). The interplexiform cell system, I: Synapses of the dopaminergic neurons in the goldfish retina. Proceedings of the Royal Society B (London) 201, 726.Google Scholar
Dubocovich, M.L. (1983). Melatonin is a potent modulator of dopamine release in the retina. Nature 306, 782784.CrossRefGoogle ScholarPubMed
Dubocovich, M.L., Lucas, R.C. & Takahashi, J.S. (1985). Light-dependent regulation of dopamine receptors in mammalian retina. Brain Research 335, 321325.CrossRefGoogle ScholarPubMed
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
Iuvone, P.M., Galli, C.L., Garrison-Gund, C.K. & Neff, N.H. (1978). Light stimulates tyrosine-hydroxylase activity and dopamine synthesis in retinal amacrine neurons. Science 202, 901902.CrossRefGoogle ScholarPubMed
John, K., Segall, M. & Zawatsky, L. (1967). Retinomotor rhythms in the goldfish (Carassius auratus). Biological Bulletin 132, 200210.CrossRefGoogle ScholarPubMed
Kirsch, M. & Wagner, H.-J. (1989). Release pattern of endogenous dopamine in teleost retinae during light adaptation and pharmacological stimulation. Vision Research 29, 147154.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 10, 438452.Google ScholarPubMed
Levinson, G. & Burnside, B. (1981). Circadian rhythms in teleost retinomotor movements. A comparison of the effects of circadian rhythm and light condition on cone length. Investigative Ophthalmology and Visual Science 20, 294303.Google 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
Nowak, J.Z. & Zurawska, E. (1989). Dopamine in the rabbit retina and striatum: diurnal rhythm and effect of light stimulation. Journal of Neural Transmission 75, 201212.CrossRefGoogle ScholarPubMed
Parkinson, D. & Rando, R.R. (1983). Effects of light on dopamine metabolism in the chick retina. Journal of Neurochemistry 40, 3946.CrossRefGoogle ScholarPubMed
Pierce, M.E. & Besharse, J.C. (1985). Circadian regulation of retinomotor movements, I: Interactions of melatonin and dopamine in the control of cone length. Journal of General Physiology 86, 671689.CrossRefGoogle ScholarPubMed
Teranishi, T., Negishi, K. & Kato, S. (1984). Regulatory effect of dopamine on spatial properties of horizontal cells in carp retina. Journal of Neuroscience 4, 12711280.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
Welsh, J.H. & Osborn, C.M. (1937). Diurnal changes in the retina of the catfish (Ameiurus nebulosus). Journal of Comparative Neurology 66, 349359.CrossRefGoogle Scholar
Wirz-Justice, A., Da Prada, M. & Reme, C. (1984). Circadian rhythm in rat retinal dopamine. Neuroscience Letters 45, 2125.CrossRefGoogle ScholarPubMed
Witkovsky, P., Stone, S. & Besharse, J.C. (1988 a). The effects of dopamine and related ligands on photoreceptor to horizontal cell transfer in the Xenopus retina. Biomedical Research 9, 93107.Google Scholar
Witkovsky, P., Stone, S. & Besharse, J.C. (1988 b). Dopamine modifies the balance of rod and cone inputs to horizontal cells of the Xenopus retina. Brain Research 449, 332336.CrossRefGoogle ScholarPubMed
Wirkovsky, P., Stone, S. & Tranchina, D. (1989). Photoreceptor to horizontal cell synaptic transfer in the Xenopus retina: modulation by dopamine ligands and a circuit model for interactions of rod and cone inputs. Journal of Neurophysiology 62, 864881.CrossRefGoogle Scholar