Literature DB >> 2861099

Anticonvulsant properties of 3-hydroxy-2-quinoxalinecarboxylic acid, a newly found antagonist of excitatory amino acids.

U Erez, H Frenk, O Goldberg, A Cohen, V I Teichberg.   

Abstract

Various aromatic acids have been investigated as putative ligands of excitatory amino acid receptors. 3-Hydroxy-2-quinoxalinecarboxylic acid (HQC), at 1 mM, was found to antagonize the 22Na+ efflux produced in 22Na+-preloaded brain slices by N-methyl-D-aspartate and kainate. The response to glutamate was also affected but not that to quisqualate. The apparent KI value of HQC for suppression of the N-methyl-D-aspartate response was 0.27 mM. The anticonvulsant action of HQC was investigated in mice and rats. HQC administered intracerebroventricularly caused a dose dependent delay in the occurrence of picrotoxin induced convulsions and afforded protection against picrotoxin induced death. These results confirm the proposition that antagonists of excitatory amino acids possess anticonvulsant properties.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 2861099     DOI: 10.1016/0014-2999(85)90025-1

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  2 in total

1.  Quinoxalines interact with the glycine recognition site of NMDA receptors: studies in guinea-pig myenteric plexus and in rat cortical membranes.

Authors:  D E Pellegrini-Giampietro; A Galli; M Alesiani; G Cherici; F Moroni
Journal:  Br J Pharmacol       Date:  1989-12       Impact factor: 8.739

2.  Synthesis and Biological Evaluation of Some [1,2,4]Triazolo[4,3-a]quinoxaline Derivatives as Novel Anticonvulsant Agents.

Authors:  Mohamed Alswah; Adel Ghiaty; Ahmed El-Morsy; Kamal El-Gamal
Journal:  ISRN Org Chem       Date:  2013-09-12
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.