Abstract
Accumulating preclinical data suggest that compounds that block the excitatory effect of glutamate on the kainate subtype of glutamate receptors may have utility for the treatment of pain, migraine, and epilepsy. In the present study, the in vitro pharmacological properties of the novel glutamate antagonist 5-carboxyl-2,4-di-benzamido-benzoic acid (NS3763) are described. In functional assays in human embryonic kidney (HEK)293 cells expressing homomeric GLUK5 or GLUK6 receptors, NS3763 is shown to display selectivity for inhibition of domoate-induced increase in intracellular calcium mediated through the GLUK5 subtype (IC50 = 1.6 μM) of kainate receptors compared with the GLUK6 subtype (IC50 > 30 μM). NS3763 inhibits the GLUK5-mediated response in a noncompetitive manner and does not inhibit [3H]α-amino-3-hydroxy-5-tertbutylisoxazole-4-propionic acid binding to GLUK5 receptors. Furthermore, NS3763 selectively inhibits l-glutamate- and domoate-evoked currents through GLUK5 receptors in HEK293 cells and does not significantly inhibit α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid- or N-methyl-d-aspartate-induced currents in cultured mouse cortical neurons at 30 μM. This is the first report on a selective and noncompetitive GLUK5 antagonist.
Footnotes
-
J.K.C. was supported by the Danish Academy of Technical Sciences.
-
DOI: 10.1124/jpet.103.062794.
-
ABBREVIATIONS: NMDA, N-methyl-d-aspartate; AMPA, α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid; APV, d-2-amino-5-phosphovaleric acid; NBQX, 2,3-dihydroxy-6-nitro-7-sulfamoylbenzo[f]quinoxaline; ATPA, α-amino-3-hydroxy-5-tertbutylisoxazole-4-propionic acid; GYKI52466, 1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine; NS1209, 8-methyl-5-(4-(N,N-dimethylsulfamoyl)phenyl)-6,7,8,9,-tetrahydro-1H-pyrrolo[3,2-h]-isoquinoline-2,3-dione-3-O-(4-hydroxybutyric acid-2-yl)oxime; NS3763, 5-carboxyl-2,4-di-benzamidobenzoic acid; HEK, human embryonic kidney; DMEM, Dulbecco's modified Eagle's medium; GYI53655, 1-(4-aminophenyl)-3-methylcarbamyl-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine; LY382884, 3S,4aR,6S,8aR-6-(4-carboxyphenyl)methyl-1,2,3,4,4a,5,6,7,8,8a-deca-hydroisoquinoline-3-carboxylic acid; NS102, 5-nitro-6,7,8,9-tetrahydrobenzo[g]indole-2,3-dione-3-oxime.
- Received November 10, 2003.
- Accepted February 24, 2004.
- The American Society for Pharmacology and Experimental Therapeutics
JPET articles become freely available 12 months after publication, and remain freely available for 5 years.Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page.
|