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Dextromethorphan: cellular effects reducing neuronal hyperactivity.
Trube, G; Netzer, R.
Affiliation
  • Trube G; Pharma Division, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
Epilepsia ; 35 Suppl 5: S62-7, 1994.
Article in En | MEDLINE | ID: mdl-7518769
ABSTRACT
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 antiepileptic 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.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Dextromethorphan / Ion Channels Limits: Animals / Humans Language: En Journal: Epilepsia Year: 1994 Type: Article Affiliation country: Switzerland
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Dextromethorphan / Ion Channels Limits: Animals / Humans Language: En Journal: Epilepsia Year: 1994 Type: Article Affiliation country: Switzerland