Literature DB >> 6253533

Postnatal development of GABA-ergic neurons in the rabbit retina.

D M Lam, S C Fung, Y C Kong.   

Abstract

Uptake, synthesis, storage, and release of gamma-aminobutyric acid (GABA) are some of the characteristic properties of GABA-ergic neurons. In the present study, we have used these properties as physiological probes to follow the emergence and maturation of GABA-ergic neurons during postnatal development of the rabbit retina. There is autoradiographic, immunocytochemical, and pharmacological evidence that some amacrine cells and certain neurons in the ganglion cell layer probably use GABA as the neurotransmitter. These neurons take up GABA, contain the GABA-synthesizing enzyme L-glutamic acid decarboxylase (GAD, EC 4.1.1.15), and release the accumulated GABA by a CA++-dependent mechanism when depolorized with high extracellular K+ concentration. In this study, we show that certain neurons in the newborn retina already possess a specific mechanism for GABA uptake. The positions and numbers of these cells in the developing retina suggest that they will become GABA-ergic neurons in the adult retina. These putative GABA-ergic neurons are, however, probably immature at birth because newborn retinas contain only low levels of GABA and GAD. Additionally, there is relatively little K+-stimulated, Ca++-dependent release of (3H)-GABA from the newborn retinas. GABA concentrations and GAD activities in developing retinas increase steadily postnatally, reaching about 80% of the adult levels by day 9. The activities of the GABA-degrading enzyme, GABA-glutamate transaminase (GABA-T, EC 2.6.1.19), follow a similar pattern of maturation during retinal development. K+ stimulated GABA release, however, remains low until about day 6, and then increases dramatically from 20% to 85% of the adult level over the next 3 days. Taken together, our results indicate that in the rabbit retina, the commitment by certain neurons to use GABA as the transmitter is made prenatally. These neurons are immature at birth but are biochemically, physiologically, and probably functionally mature by about 9 days after birth.

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Year:  1980        PMID: 6253533     DOI: 10.1002/cne.901930107

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  6 in total

1.  Light and dark adaptation influences GABA receptor sites in the chick retina.

Authors:  S Fiszer de Plazas; J Alfie; N N González
Journal:  Neurochem Res       Date:  1986-07       Impact factor: 3.996

2.  GABA neurones in retinas of different species and their postnatal development in situ and in culture in the rabbit retina.

Authors:  N N Osborne; S Patel; D W Beaton; V Neuhoff
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

3.  [3H]GABA binding in developing rabbit retina.

Authors:  P Madtes; D A Redburn
Journal:  Neurochem Res       Date:  1982-04       Impact factor: 3.996

4.  The occurrence of gamma-aminobutyric acid (GABA)-containing cells in cultures of retinas from the human fetus.

Authors:  N N Osborne; D W Beaton
Journal:  Cell Mol Neurobiol       Date:  1986-03       Impact factor: 5.046

5.  Dopaminergic neurones in various retinas and the postnatal development of tyrosine-hydroxylase immunoreactivity in the rabbit retina.

Authors:  N N Osborne; S Patel; A Vigny
Journal:  Histochemistry       Date:  1984

6.  L-glutamic acid: a neurotransmitter candidate for cone photoreceptors in human and rat retinas.

Authors:  C Brandon; D M Lam
Journal:  Proc Natl Acad Sci U S A       Date:  1983-08       Impact factor: 11.205

  6 in total

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