A quantitative autoradiographic assay for a novel -[3H]glutamate binding site in rodent brain has been developed. Binding to this site was distinguished by its high affinity for quisqualate (QA), ibotenate, glutamate and trans-1-amino-cyclopentyl-1,3-dicarboxylic acid (trans-ACPD), but low affinity for [RS]-[alpha]-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), kainate and (NMDA). `AMPA-insensitive, QA-sensitive [3H]glutamate binding' (AiQsGB) had a heterogeneous distribution in rat brain with high levels observed in molecular layer of cerebellum, striatum, and lateral septum. AiQsGB was reduced in molecular layer of cerebellum in mice lacking Purkinje cells. AiQsGB appears to represent binding to the `metabotropic' neuronal ex...
Abstract: Quisqualate, a glutamate analogue, displaced L-[3H]glutamate binding in a biphasic manner,...
Quantitative autoradiography was used to examine the density and distribution of excitatory amino ac...
Kainic acid is supposed to be a specific agonist for a subclass of excitatory glutamate receptors in...
Glutamate is the major neurotransmitter mediating excitatory signalling within the mammalian central...
Using quantitative autoradiography, we have investigated the binding sites for the potent competitiv...
A quantitative autoradiographic technique was developed to study L- ('3)H glutamate binding in secti...
Excitatory amino acids (EAA) such as glutamate and aspartate are probably the neurotransmitters of a...
Quisqualate, a glutamate analogue, displaced L-[ 3 H]glutamate binding in a biphasic manner, corresp...
Using quantitative autoradiography, the cellular localization and characterization of cerebellar exc...
Quantitative autoradiography was used to characterize the phar-macological specificity and anatomica...
AbstractAntibodies were made to a thirteen amino acid synthetic peptide corresponding to the C-termi...
Calcium and chloride ions stimulated [3H]glutamate binding to quisqualate-sensitive [3H]glutamate bi...
The Naples high-excitability (NHE) and low-excitability (NLE) rat lines, selectively bred for high a...
Quantitative receptor autoradiography was used to determine the distribution of excitatory amino aci...
Striatal binding of labeled glutamate to (NMDA) receptors, -[alpha]-amino-3-hydroxy-5-methyl-4-isox...
Abstract: Quisqualate, a glutamate analogue, displaced L-[3H]glutamate binding in a biphasic manner,...
Quantitative autoradiography was used to examine the density and distribution of excitatory amino ac...
Kainic acid is supposed to be a specific agonist for a subclass of excitatory glutamate receptors in...
Glutamate is the major neurotransmitter mediating excitatory signalling within the mammalian central...
Using quantitative autoradiography, we have investigated the binding sites for the potent competitiv...
A quantitative autoradiographic technique was developed to study L- ('3)H glutamate binding in secti...
Excitatory amino acids (EAA) such as glutamate and aspartate are probably the neurotransmitters of a...
Quisqualate, a glutamate analogue, displaced L-[ 3 H]glutamate binding in a biphasic manner, corresp...
Using quantitative autoradiography, the cellular localization and characterization of cerebellar exc...
Quantitative autoradiography was used to characterize the phar-macological specificity and anatomica...
AbstractAntibodies were made to a thirteen amino acid synthetic peptide corresponding to the C-termi...
Calcium and chloride ions stimulated [3H]glutamate binding to quisqualate-sensitive [3H]glutamate bi...
The Naples high-excitability (NHE) and low-excitability (NLE) rat lines, selectively bred for high a...
Quantitative receptor autoradiography was used to determine the distribution of excitatory amino aci...
Striatal binding of labeled glutamate to (NMDA) receptors, -[alpha]-amino-3-hydroxy-5-methyl-4-isox...
Abstract: Quisqualate, a glutamate analogue, displaced L-[3H]glutamate binding in a biphasic manner,...
Quantitative autoradiography was used to examine the density and distribution of excitatory amino ac...
Kainic acid is supposed to be a specific agonist for a subclass of excitatory glutamate receptors in...