Literature DB >> 7207695

Primary afferent depolarization. Distribution of the gamma-aminobutyric acid system in frog spinal cord.

S Glusman, M Pacheco, D McAdoo, B Haber.   

Abstract

In the frog spinal cord primary afferent depolarization (PAD) constitutes a powerful inhibitory control mechanism. It has been suggested that gamma-aminobutyric acid (GABA) is the transmitter substance involved in the genesis of PAD. In these studies we show that maximal glutamic acid decarboxylase activity is localized roughly 400-600 micrometers from the dorsal surface, and that correlates well with the intraspinal distribution of field potentials associated with PAD. Measurements of GABA in serial spinal cord sections cut in a dorsal--ventral direction shows that high levels of GABA are seen at 400--600 micrometers, with a peak at 800 micrometers from the dorsal surface. Stimulation at frequencies shown to produce PAD augments the release of endogenous GABA from a superfused frog hemicord preparation.

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Year:  1980        PMID: 7207695     DOI: 10.1007/bf00966141

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  21 in total

1.  Amino acid concentrations in the Aplysia nervous system: neurons with high glycine concentrations.

Authors:  T M Iliffe; D J McAdoo; C B Beyer; B Haber
Journal:  J Neurochem       Date:  1977-05       Impact factor: 5.372

2.  Correlation between the topographical distribution of [3H]GABA uptake and primary afferent depolarization in the frog spinal cord.

Authors:  S Glusman
Journal:  Brain Res       Date:  1975-04-25       Impact factor: 3.252

3.  Depolarization of central terminals of Group I afferent fibres from muscle.

Authors:  J C Eccles; F Magni; W D Willis
Journal:  J Physiol       Date:  1962-01       Impact factor: 5.182

Review 4.  The role of GABA in primary afferent depolarization.

Authors:  R A Levy
Journal:  Prog Neurobiol       Date:  1977       Impact factor: 11.685

5.  Dorsal root potentials of the spinal cord.

Authors:  J C ECCLES; J L MALCOLM
Journal:  J Neurophysiol       Date:  1946-05       Impact factor: 2.714

6.  The release of amino acids from the hemisected spinal cord during stimulation.

Authors:  P J Roberts; J F Mitchell
Journal:  J Neurochem       Date:  1972-11       Impact factor: 5.372

7.  GABA-transaminase inhibitors and presynaptic inhibition in the amphibian spinal cord.

Authors:  R A Davidoff; V Grayson; R Adair
Journal:  Am J Physiol       Date:  1973-05

8.  The pharmacology and ionic dependency of amino acid responses in the frog spinal cord.

Authors:  J L Barker; R A Nicoll
Journal:  J Physiol       Date:  1973-01       Impact factor: 5.182

9.  The filum terminale of the frog spinal cord, a non transformed preparation: I. Morphology and uptake of gamma-aminobutyric acid.

Authors:  S Glusman; M Pacheco; A González Robles; B Haber
Journal:  Brain Res       Date:  1979-08-24       Impact factor: 3.252

10.  The release of gamma-aminobutyric acid during inhibition in the cat visual cortex.

Authors:  L L Iversen; J F Mitchell; V Srinivasan
Journal:  J Physiol       Date:  1971-01       Impact factor: 5.182

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