Abstract
NBQX (2,3-Dihydroxy-6-nitro-7-sulphamoyl-benzo(f)quinoxaline) was found to be a potent and selective ligand for quisqualate and kainate receptors.
Furthermore, it is a selective antagonist of non-NMDA responses in the rat neocortex, and of AMPA and kainate evoked neurotoxicity in cultured neurones.
NBQX (30 mg/kg) given pre and post or just post ischaemia, to Mongolian gerbils having received 5 min bilateral carotid artery occlusion, produced a clear neuroprotective effect. This is the first in vivo demonstration of a selective quisqualate/kainate antagonist showing neuroprotective properties.
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© 1990 ESCOM Science Publishers B.V.
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Sheardown, M.J., Nielsen, E.Ă˜., Drejer, J., HonorĂ©, T. (1990). 2,3-Dihydroxy-6-nitro-7-sulphamoyl-benzo(f)quinoxaline, a selective non-N-methyl-D-aspartate excitatory amino acid receptor antagonist, has neuroprotective properties in a model of transient global ischaemia. In: Lubec, G., Rosenthal, G.A. (eds) Amino Acids. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-2262-7_59
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DOI: https://doi.org/10.1007/978-94-011-2262-7_59
Publisher Name: Springer, Dordrecht
Print ISBN: 978-90-72199-04-1
Online ISBN: 978-94-011-2262-7
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