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PMID: 1902921 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Calcium-dependent release of accumulated glutamate from synaptic vesicles within permeabilized nerve terminals.

Neuroscience letters ·Vol. 122 ·No. 2 ·1991-01-28 ·Pages 179-82

Kish PE, Ueda T

Abstract

We have studied glutamate release from synaptic vesicles in permeabilized synaptosomes, which were preloaded with [3H]glutamate in an ATP-dependent manner. The release was found to be calcium-dependent and to require a heat-labile cytosolic macromolecule factor for maximum activity. Maximal release occurred at 5 microM free Ca2+ and within 5 min. Of the other divalent cations tested, only barium stimulated release of vesicular glutamate. The release was inhibited by N-ethylmaleimide. These results are characteristic of exocytotic release of monoamines and peptides observed in endocrine systems, and constitute direct evidence for the notion that calcium-dependent release of glutamate originates from the vesicular pool.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Brain/drug effects,metabolism Calcium/pharmacology Cations, Divalent Egtazic Acid/pharmacology Glutamates/metabolism Kinetics Nerve Endings/drug effects,metabolism Permeability Rats Synaptic Vesicles/drug effects,metabolism Synaptosomes/drug effects,metabolism
Chemicals
Cations, Divalent Glutamates Egtazic Acid Adenosine Triphosphate Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kish P E
Mental Health Research Institute, University of Michigan, Ann Arbor 48109.
Ueda T
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1991-01-28
Pages
179-82
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
Grants
NIMH NIH HHS · 5P01 MH 42652 · United States
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