We have identified specific high-affinity [3H]dextrorphan binding sites in rat forebrain. [3H]Dextrorphan binds saturably and reversibly to an apparently homogeneous class of sites characterized by a Bmax of 2.62±0.06 pmol/mg protein and KD of 60±4 nM. Glycine and glutamate independently increase [3H]dextrorphan binding in a concentration-dependent manner. The pharmacological profile of [3H]dextrorphan binding characterized by equilibrium competition experiments, together with these data suggest that [3H]dextrorphan labels a site at or near the N-methyl-D-aspartate receptor.
|Original language||English (US)|
|Number of pages||5|
|Journal||European Journal of Pharmacology: Molecular Pharmacology|
|State||Published - Jul 31 1990|
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