Literature DB >> 1931794

The organization of dopaminergic neurons in vertebrate retinas.

P Witkovsky1, M Schütte.   

Abstract

A survey of the shapes of dopaminergic (DA) neurons in the retinas of representative vertebrates reveals that they are divisible into three groups. In teleosts and Cebus monkey, DA cells are interplexiform (IPC) neurons with an ascending process that ramifies to create an extensive arbor in the outer plexiform layer (OPL). All other vertebrates studied, including several primate species, have either DA amacrine cells or IPCs with an ascending process that either does not branch within the OPL or does so to a very limited degree. DA neurons of non-teleosts exhibit a dense plexus of fine caliber fibers which extends in the distal most sublamina of the inner plexiform layer (IPL). Teleosts lack this plexus. In all vertebrates, DA cells are distributed more or less evenly and at a low density (10-60 cells/mm2) over the retinal surface. Dendritic fields of adjacent DA neurons overlap. Most of the membrane area of the DA cell is contained within the plexus of fine fibers, which we postulate to be the major source of dopamine release. Thus, dopamine release can be modeled as occurring uniformly from a thin sheet located either in the OPL (teleosts) or in the distal IPL (most other vertebrates) or both (Cebus monkey). Assuming that net lateral spread of dopamine is zero, the fall of dopamine concentration with distance at right angles to the sheet (i.e. in the scleral-vitreal axis) will be exponential. The factors that influence the rate of fall-diffusion in extracellular space, uptake, and transport--are not yet quantified for dopamine, hence the dopamine concentration around its target cells cannot yet be assessed. This point is important in relation to the thresholds for activation of D1 and D2 dopamine receptors that are found on a variety of retinal cells.

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Year:  1991        PMID: 1931794     DOI: 10.1017/s0952523800010981

Source DB:  PubMed          Journal:  Vis Neurosci        ISSN: 0952-5238            Impact factor:   3.241


  18 in total

1.  Somatostatin modulates voltage-gated K(+) and Ca(2+) currents in rod and cone photoreceptors of the salamander retina.

Authors:  A Akopian; J Johnson; R Gabriel; N Brecha; P Witkovsky
Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

Review 2.  Circadian phototransduction and the regulation of biological rhythms.

Authors:  Mario E Guido; Agata R Carpentieri; Eduardo Garbarino-Pico
Journal:  Neurochem Res       Date:  2002-11       Impact factor: 3.996

3.  Gene discovery in genetically labeled single dopaminergic neurons of the retina.

Authors:  Stefano Gustincich; Massimo Contini; Manuela Gariboldi; Michelino Puopolo; Koji Kadota; Hidemasa Bono; Julianna LeMieux; Pamela Walsh; Piero Carninci; Yoshihide Hayashizaki; Yasushi Okazaki; Elio Raviola
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-26       Impact factor: 11.205

4.  Alterations in visual receptive fields in the superior colliculus induced by amphetamine.

Authors:  K L Grasse; R M Douglas; J R Mendelson
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

5.  Brain-derived neurotrophic factor modulates the development of the dopaminergic network in the rodent retina.

Authors:  A Cellerino; G Pinzón-Duarte; P Carroll; K Kohler
Journal:  J Neurosci       Date:  1998-05-01       Impact factor: 6.167

6.  Cellular location and circadian rhythm of expression of the biological clock gene Period 1 in the mouse retina.

Authors:  Paul Witkovsky; Eleonora Veisenberger; Joseph LeSauter; Lily Yan; Madeleine Johnson; Dao-Qi Zhang; Douglas McMahon; Rae Silver
Journal:  J Neurosci       Date:  2003-08-20       Impact factor: 6.167

Review 7.  Dopamine and retinal function.

Authors:  Paul Witkovsky
Journal:  Doc Ophthalmol       Date:  2004-01       Impact factor: 2.379

8.  Some horizontal cells of the bovine retina receive input synapses in the inner plexiform layer.

Authors:  M H Chun; H Wässle
Journal:  Cell Tissue Res       Date:  1993-06       Impact factor: 5.249

9.  Facilitation of GABAergic signaling in the retina by receptors stimulating adenylate cyclase.

Authors:  A Feigenspan; J Bormann
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-08       Impact factor: 11.205

10.  Dopamine receptor loss of function is not protective of rd1 rod photoreceptors in vivo.

Authors:  Judith Mosinger Ogilvie; Angela M Hakenewerth; Rachel R Gardner; Joshua G Martak; Virginia M Maggio
Journal:  Mol Vis       Date:  2009-12-23       Impact factor: 2.367

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