H-3-L-glutamate binding and H-3-D-aspartate release from hippocampal tissue during the development of pentylenetetrazole kindling in rats

Citation
H. Schroeder et al., H-3-L-glutamate binding and H-3-D-aspartate release from hippocampal tissue during the development of pentylenetetrazole kindling in rats, PHARM BIO B, 62(2), 1999, pp. 349-352
Citations number
23
Categorie Soggetti
Neurosciences & Behavoir
Journal title
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
ISSN journal
00913057 → ACNP
Volume
62
Issue
2
Year of publication
1999
Pages
349 - 352
Database
ISI
SICI code
0091-3057(199902)62:2<349:HBAHRF>2.0.ZU;2-J
Abstract
Previous studies have proposed that there is an increase in the density of glutamate binding sites after pentylenetetrazol (PTZ) kindling, whereas the glutamate release is not altered. Little is known about the time course of these changes. Therefore, we studied H-3-L-glutamate binding to hippocampa l membranes and K+-stimulated H-3-D-aspartate release from hippocampal slic es of rats given PTZ 3, 7, and 13 times up to a fully kindling state. After three PTZ injections, amino acid release from hippocampal tissue slices wa s significantly enhanced in comparison to controls, whereas H-3-L-glutamate binding was not altered. After seven injections of PTZ, specific glutamate binding to hippocampal membranes tended to increase, and K+-stimulated H-3 -D-aspartate release from rat hippocampal slices was normalized. The kindle d state characterized by generalized clonic-tonic seizures was reached afte r 13 PTZ injections, and it was accompanied by an enhancement in the densit y of glutamate binding sites, whereas the chemically evoked amino acid rele ase remained unchanged. It can be concluded that the amino acid release is increased in the early phase of PTZ kindling development, whereas after com pletion of kindling, the density of excitatory amino acid binding sites is enhanced. (C) 1999 Elsevier Science Inc.