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Darkness stimulates rapid synthesis and release of melatonin in rat retina

Published online by Cambridge University Press:  02 June 2009

Dianna A. Redburn
Affiliation:
Department of Neurobiology and Anatomy, The University of Texas Medical School, Houston
Cheryl K. Mitchell
Affiliation:
Department of Neurobiology and Anatomy, The University of Texas Medical School, Houston

Abstract

The presence of melatonin in retina has been widely reported for over two decades although studies of its functional importance within the retina have only recently been emphasized. We have analyzed the biochemical characteristics of melatonin synthesis and release, focusing on rapid changes in response to light/dark conditions. Our major findings are consistent with the following conclusions: (1) melatonin synthesis is stimulated within minutes after exposure to darkness, and may reflect an increase in N-acetyl transferase activity; (2) melatonin is not stored, but rather it diffuses freely throughout the retina immediately after it is synthesized; and (3) the dark-induced increase in retinal melatonin release is a synthesis-coupled response and does not involve separate secretion mechanisms. The characteristics of melatonin synthesis and release described herein would be consistent with the proposed role of melatonin as a local paracrine effector of dark-adaptive responses in retina.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1989

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References

Besharse, J.C. & Dunis, D.A. (1983). Methoxyindoles and photoreceptor metabolism: activation of rod shedding. Science 219, 13411343.CrossRefGoogle ScholarPubMed
Binkley, S., Hryshchyshyn, M. & Reilly, K. (1979). N-acetyltransferase activity responds to environmental lighting in the eye as well as in the pineal gland. Nature 281, 479481.CrossRefGoogle ScholarPubMed
Cardinali, D.P. & Rosner, J.M. (1971). Metabolism of serotonin by the rat retina in vitro. Journal of Neurochemistry 18, 1769.CrossRefGoogle ScholarPubMed
Dearry, A. & Burnside, B. (1986). Dopaminergic regulation of cone retinomotor movement in isolated teleost retinas, II: Modulation by gamma-aminobutyric acid and serotonin. Journal of Neurochemistry 46, 10221031.CrossRefGoogle ScholarPubMed
Dubocovich, M.L. (1983). Melatonin is a potent modulator of dopamine release in the retina. Nature 306, 782784.CrossRefGoogle ScholarPubMed
Hamm, H.E. & Menaker, M. (1980). Retinal rhythms in chicks–circadian variation in melatonin and serotonin N-acetyltransferase activity. Proceedings of the National Academy of Sciences of the U.S.A. 77, 49985002.CrossRefGoogle ScholarPubMed
Iuvone, P.M. & Besharse, J.C. (1986 a). Cyclic AMP stimulates serotonin N-acetyltransferase activity in Xenopus retina in vitro. Journal of Neurochemistry 46, 3339.CrossRefGoogle ScholarPubMed
Iuvone, P.M. & Besharse, J.C. (1986 b). Involvement of calcium in the regulation of serotonin N-acetyltransferase in retina. Journal of Neurochemistry 46, 8288.CrossRefGoogle ScholarPubMed
Klein, D.C. (1979). Circadian rhythms in the pineal gland. In Endocrine Rhythms, ed. Krieger, D.T., pp. 203223New York: Raven Press.Google Scholar
Klein, D.C. & Berg, G.R. (1970). Pineal gland: stimulation of melatonin production by norepinephrine involves cyclic AMP-mediated stimulation of N-acetyltransferase. Advances in Biochemical Psychopharmacology 3, 241263.Google ScholarPubMed
Klein, D.C., Sugden, D. & Weller, J.L. (1983). Postsynaptic α-adrenergic receptors potentiate the í-adrenergic stimulation of pineal serotonin N-acetyltransferase. Proceedings of the National Academy of Sciences of the U.S.A. 80, 599603.CrossRefGoogle Scholar
Klein, D.C. & Weller, J.L. (1970). Indole metabolism in the pineal gland: a circadian rhythm in N-acetyltransferase. Science 169, 10931095.CrossRefGoogle ScholarPubMed
Krasovich, M. & Benson, B. (1983). Effects of melatonin on the retina of the golden Syrian hamster. Anatomical Record 205, A102.Google Scholar
Lasater, E. & Dowling, J.E. (1985). Dopamine decreases conductance of electrical junctions between cultured retinal horizonal cells. Proceedings of the National Academy of Sciences of the U.S.A. 82, 30253029.CrossRefGoogle Scholar
Massey, S.C. & Redburn, D.A. (1987). Transmitter circuits in the vertebrate retina. Progress in Neurobiology 28, 5596.CrossRefGoogle ScholarPubMed
Nagle, C.A., Cardinali, D.P. & Rosner, J.M. (1973). Retinal and pineal hydroxyindole-O-methyl transferases in the rat: changes following cervical sympathectomy, pinealectomy, or blinding. Endocrinology 92, 15601564.CrossRefGoogle ScholarPubMed
Neyton, J., Piccolino, M. & Gerschenfeld, H.M. (1982). Dopamine and drugs that increase intracellular cyclic AMP decrease junctional communication between L-horizontal cells. Society for Neuroscience Abstracts 8, 132.Google Scholar
Pang, S.F. & Allen, A.E. (1986). Extra-pineal melatonin in retina: its regulation and physiological function. Pineal Research Reviews 4, 5595.Google Scholar
Pang, S.F. & Yew, D.T. (1979). Pigment aggregation by melatonin in the retinal-pigment epithelium and choroid of guinea pigs, caviaporcellus. Experientia 35, 231233.CrossRefGoogle ScholarPubMed
Pang, S.F., Yu, H.S., Suen, H.C. & Brown, G.M. (1980). Melatonin in the retina of rats: a diurnal rhythm. Journal of Endocrinology 87, 8993.CrossRefGoogle ScholarPubMed
Pang, S.F., Yu, H.S. & Tang, P.L. (1981). A diurnal rhythm of Nacetylserotonin in the retina of rats. Neuroscience Letters 21, 197200.CrossRefGoogle ScholarPubMed
Pautler, E.L. & Hall, F.L. (1987). Movement of melatonin across the retinal pigment epithelium. Experimental Eye Research 45, 351355.CrossRefGoogle ScholarPubMed
Quay, W.B. (1965). Retinal and pineal hydroxyindole-O-methyltransferase activity in vertebrates. Life Sciences 4, 983.CrossRefGoogle Scholar
Quay, W.B. & McLeod, R.W. (1968). Melatonin and photic stimulation of cone contraction in the retina of larval Xenopus laevis. Anatomical Record 160, 491.Google Scholar
Redburn, D.A. (1977). Analysis of lsqb;14C/-GABA uptake and release from rabbit retina synaptosomes. Experimental Eye Research 25, 265275.CrossRefGoogle Scholar
Redburn, D.A. & Churchill, L. (1987). An indoleamine system in photoreceptor cell terminals of the Long-Evans rat retina. Journal of Neuroscience 7, 319329.CrossRefGoogle ScholarPubMed
Reppert, S.M. & Sagar, S.M. (1983). Characterization of the daynight variation of retinal melatonin content in the chick. Investigative Ophthalmology and Visual Science 24, 294300.Google ScholarPubMed
Snyder, S.H., Shaskan, E.G. & Kukar, M.J. (1973). Serotonin uptake systems in brain tissue. In Serotonin and Behavior, ed. Barchas, J. & Usdin, E., pp. 97108. New York: Academic Press.Google Scholar
Vivien-Roels, B., Pevet, P., Dubois, M.P., Arendt, J. & Brown, G.M. (1981). Immunohistochemical evidence for the presence of melatonin in the pineal gland, the retina, and Harderian gland. Cell and Tissue Research 217, 105115.CrossRefGoogle ScholarPubMed
White, M.P. & Fisher, L.J. (1980). Melatonin effects on circadian rod outer segment shedding. Society for Neurosceince Abstracts 6, 344.Google Scholar
Wiechmann, A.F., Bok, D. & Horwitz, J. (1985). Localization of hydroxyindole-O-methyltransferase in the mammalian pineal gland and retina. Investigative Ophthalmology Visual Science 26, 253265.Google ScholarPubMed
Wiechmann, A.F. (1986). Melatonin: parallels in pineal gland and retina. Experimental Eye Research 42, 507527.CrossRefGoogle ScholarPubMed
Yu, H.S., Chow, P.H., Tang, P.L. & Pang, S.F. (1982). Effect of light and darkness on the in vitro release of N-acetylserotonin and melatonin by the retina of guinea pigs. Neuroendocrinology 34, 265268.CrossRefGoogle ScholarPubMed
Yu, H.S., Pang, S.F., Tang, P.L. & Brown, G.M. (1981). Persistence of circadian rhythms of melatonin and N-acetylserotonin in the serum of rats after pinealectomy. Neuroendocrinology 32, 262265.CrossRefGoogle ScholarPubMed