June 1994
Volume 35, Issue 7
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Articles  |   June 1994
Immunohistochemical localization of L-dopa and aromatic L-amino acid-decarboxylase in the rat retina.
Author Affiliations
  • J Nguyen-Legros
    Laboratoire de Neurocytologie Oculaire, INSERM U-86, Paris, France.
  • M Krieger
    Laboratoire de Neurocytologie Oculaire, INSERM U-86, Paris, France.
  • A Simon
    Laboratoire de Neurocytologie Oculaire, INSERM U-86, Paris, France.
Investigative Ophthalmology & Visual Science June 1994, Vol.35, 2906-2915. doi:
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    • Get Citation

      J Nguyen-Legros, M Krieger, A Simon; Immunohistochemical localization of L-dopa and aromatic L-amino acid-decarboxylase in the rat retina.. Invest. Ophthalmol. Vis. Sci. 1994;35(7):2906-2915.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: The purpose of this study was threefold: to determine if some catecholaminergic amacrine cells of the rat retina use L-DOPA as their neurotransmitter, especially the small (2CA) cells that are immunoreactive to tyrosine hydroxylase but not to dopamine; to understand better the possible existence of serotoninergic cells in the rat retina; and to clarify the role of serotonin in the metabolism of melatonin. METHODS: Immunohistochemistry using antibodies against tyrosine hydroxylase (TH), L-DOPA, aromatic L-amino acid decarboxylase (AADC), dopamine (DA), and tyramine in rat retinal wholemounts, serial sections, and various combinations of double labeling. RESULTS: Paired wholemounts immunoreacted with anti-TH/AADC antibodies did not show a significant difference in densities of TH+ and AADC+ amacrine cells. All the TH+ cells exhibited AADC immunoreactivity. There were no AADC-immunoreactive cells lacking TH. A few TH+ cells exhibited L-DOPA immunoreactivity; they also contained AADC. The inner segments of photoreceptor cells were labeled by the anti-AADC antibody. The antibody to tyramine did not label any cells in the rat retina. CONCLUSIONS: L-DOPA can be excluded as a candidate active substance for the small TH+ amacrine cells that do not exhibit DA-immunoreactivity. The L-DOPA-immunoreactivity restricted to a small number of large TH+ amacrine cells probably does not represent an end product. Tyramine also does not appear to constitute a neurotransmitter in the rat retina. We confirm that there are no serotonin-synthesizing amacrine cells in the rat retina. The localization of AADC-immunoreactivity in the photoreceptor cell inner segments is possibly related to the biosynthetic pathway of melatonin from 5-hydroxytryptophan.

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