Literature DB >> 3587501

Uptake, exchange, and release of GABA by cerebellar glomeruli.

D M Terrian, C L Green, R V Dorman, P H Wu.   

Abstract

Glomerular particles were isolated from the bovine cerebellar vermis and studied in vitro to further assess the possibility that gamma-aminobutyric acid (GABA) is utilized as a neurotransmitter in this synaptic complex. Cerebellar glomeruli accumulated [3H]GABA at two different high affinity sites, with affinities (KT) of 2.2 X 10(-6) M and 3.0 X 10(-5) M. These uptake sites could not be distinguished on the basis of their temperature sensitivities, sodium dependence, substrate specificities or responses to metabolic inhibitors. Although an exchange process contributed to the uptake measured in these experiments, a considerable amount of the [3H]GABA accumulated by glomerular particles was stored in an osmotically-sensitive, nonexchangeable pool. Glomerular particles preloaded with [3H]GABA exhibited a Ca2+-independent release of this amino acid in response to membrane depolarization. However, when preloaded glomerular particles were exposed to unlabeled GABA, which presumably displaced [3H]GABA from the exchangeable pool, a K+-evoked and Ca2+-dependent release of the remaining [3H]GABA occurred. The observed net uptake, together with the depolarization-induced and Ca2+-dependent release, of [3H]GABA from glomerular particles supports the suggestion that functionally active GABAergic synapses are present in these structures.

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Year:  1987        PMID: 3587501     DOI: 10.1007/bf00972290

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


  31 in total

1.  GABA and glutamate uptake by subcellular fractions enriched in synaptosomes: critical evaluation of some methodological aspects.

Authors:  G Levi; M Raiteri
Journal:  Brain Res       Date:  1973-07-16       Impact factor: 3.252

2.  Competitive inhibition of GABA uptake in rat brain slices by some GABA analogues of restricted conformation.

Authors:  P M Beart; G A Johnston; M L Uhr
Journal:  J Neurochem       Date:  1972-08       Impact factor: 5.372

Review 3.  Bioenergetics of neurotransmitter transport.

Authors:  B I Kanner
Journal:  Biochim Biophys Acta       Date:  1983-12-30

4.  A simple apparatus for studying the release of neurotransmitters from synaptosomes.

Authors:  M Raiteri; F Angelini; G Levi
Journal:  Eur J Pharmacol       Date:  1974-03       Impact factor: 4.432

5.  Effects of elevated [K+]O on the release of neurotransmitters from cortical synaptosomes: efflux or secretion?

Authors:  J W Haycock; W B Levy; L A Denner; C W Cotman
Journal:  J Neurochem       Date:  1978-05       Impact factor: 5.372

6.  Amino acid uptake, content, and metabolism by neuronal and glial enriched cellular fractions from mouse cerebellum.

Authors:  R P Shank; G L Campbell
Journal:  J Neurosci       Date:  1984-01       Impact factor: 6.167

7.  Ion dependency of uptake and release of GABA and (RS)-nipecotic acid studied in cultured mouse brain cortex neurons.

Authors:  O M Larsson; J Drejer; L Hertz; A Schousboe
Journal:  J Neurosci Res       Date:  1983       Impact factor: 4.164

Review 8.  Inhibitors of the GABA uptake systems.

Authors:  P Krogsgaard-Larsen
Journal:  Mol Cell Biochem       Date:  1980-06-18       Impact factor: 3.396

9.  Energetics of gamma-aminobutyrate transport in rat brain synaptosomes.

Authors:  A Pastuszko; D F Wilson; M Erecinska
Journal:  J Biol Chem       Date:  1982-07-10       Impact factor: 5.157

10.  Sodium-dependent efflux of [3H]GABA from synaptosomes probably related to mitochondrial calcium mobilization.

Authors:  M E Sandoval
Journal:  J Neurochem       Date:  1980-10       Impact factor: 5.372

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  1 in total

1.  GABA spillover from single inhibitory axons suppresses low-frequency excitatory transmission at the cerebellar glomerulus.

Authors:  S J Mitchell; R A Silver
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

  1 in total

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