Abstract
Three compounds reportedly blocking the N-methyl-d-aspartate (NMDA) receptor, namely 2-amino-5-phosphonovalerate, γ-d-glutamylglycine and 3-hydroxy-2-quinoxalinecarboxylic acid, were injected subdurally onto the cortex of freely moving rats. All 3 compounds effectively suppressed behavioral and electrographic seizure activity induced by strychnine, morphine and picrotoxin that were administered via the same route. The cortical application of the NMDA-receptor antagonists did not induce behavioral or electrographic changes, and behavioral side-effects commonly observed following intracerebroventricular administration of these compounds were absent. The anatomical separation of anticonvulsant action and side-effects induced by these compounds suggests that this class of compounds may eventually be useful as antiepileptic drugs.
Original language | English |
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Pages (from-to) | 222-226 |
Number of pages | 5 |
Journal | Brain Research |
Volume | 373 |
Issue number | 1-2 |
DOIs | |
State | Published - 14 May 1986 |
Keywords
- 2-amino-5-phosphonovalerate
- 3-hydroxy-2-quinoxalinecarboxylic acid
- anticonvulsant
- epilepsy
- γ-d-glutamylglycine