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Dextromethorphan: Cellular Effects Reducing Neuronal Hyperactivity
Authors:G Trube  R Netzer
Institution:Pharma Division, Preclinical Research, F. Hoffmann-La Roche Ltd., Basel, Switzerland
Abstract:Summary: Dextromethorphan is a dextrorotary morphinan without affinity for opioid receptors, commonly used as an antitussive medication. During the past 5 years, interest in the compound and its demethylated derivative, dextrorphan, has been revived because additional neuroprotective and an-tiepileptic properties were found in in vitro studies, animal experiments, and a few clinical cases. Both morphinans are able to inhibit N -methyl-D-aspartate (NMDA) receptor channels and voltage-operated calcium and sodium channels with different potencies. The inhibition of the NMDA receptor is believed to be the predominant mechanism of action responsible for the anticonvulsant and neuroprotective properties of the compounds.
Keywords:Dextromethorphan–  Dextrorphan–  Drug interactions–  Receptors–  A'-methyl-D-aspartate–  Calcium-channel blockers–  Sodium channels–  Electrophysiology–  Cells  cultured–  Neurons
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