Antagonist profile of 6,7-dichloro-3-hydroxy-2-quinoxalinecarboxylate at excitatory amino acid receptors in the neonatal rat spinal cord
- 1 April 1989
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 163 (1), 127-131
- https://doi.org/10.1016/0014-2999(89)90405-6
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- 6,7-Dinitro-quinoxaline-2,3-dion and 6-nitro,7-cyano-quinoxaline-2,3-dion antagonise responses to NMDA in the rat spinal cord via an action at the strychnine-insensitive glycine receptorEuropean Journal of Pharmacology, 1988
- 7-Chlorokynurenic acid is a selective antagonist at the glycine modulatory site of the N-methyl-D-aspartate receptor complex.Proceedings of the National Academy of Sciences, 1988
- Kynurenic acid antagonises responses to NMDA via an action at the strychnine-insensitive glycine receptorEuropean Journal of Pharmacology, 1988
- Quinoxalinediones: Potent Competitive Non-NMDA Glutamate Receptor AntagonistsScience, 1988
- 6,7-Dichloro-3-hydroxy-2-quinoxalinecarboxylic acid is a relatively potent antagonist at NMDA and kainate receptorsNeuroscience Letters, 1988
- Glycine potentiates the NMDA response in cultured mouse brain neuronsNature, 1987
- CPP, a new potent and selective NMDA antagonist. Depression of central neuron responses, affinity for [3H]d-AP5 binding sites on brain membranes and anticonvulsant activityBrain Research, 1986
- Anticonvulsant properties of 3-hydroxy-2-quinoxalinecarboxylic acid, a newly found antagonist of excitatory amino acidsEuropean Journal of Pharmacology, 1985
- Excitatory Amino Acid TransmittersAnnual Review of Pharmacology and Toxicology, 1981