3H- l-Glutamate Binding and 3H- d-Aspartate Release From Hippocampal Tissue During the Development of Pentylenetetrazole Kindling in Rats

Abstract

SCHRÖEDER, H., A. BECKER, U. SCHRÖEDER AND V. HOELLT. 3H- l-Glutamate binding and K +-stimulated 3H- d-aspartate release from hippocampal tissue during the development of pentylenetetrazol-induced kindling in rats . PHARMACOL BIOCHEM BEHAV 62(2) 349–352, 1999.—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 3H- l-glutamate binding to hippocampal membranes and K +-stimulated 3H- d-aspartate release from hippocampal slices 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 was significantly enhanced in comparison to controls, whereas 3H- l-glutamate binding was not altered. After seven injections of PTZ, specific glutamate binding to hippocampal membranes tended to increase, and K +-stimulated 3H- d-aspartate release from rat hippocampal slices was normalized. The kindled state characterized by generalized clonic–tonic seizures was reached after 13 PTZ injections, and it was accompanied by an enhancement in the density of glutamate binding sites, whereas the chemically evoked amino acid release remained unchanged. It can be concluded that the amino acid release is increased in the early phase of PTZ kindling development, whereas after completion of kindling, the density of excitatory amino acid binding sites is enhanced.