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Dextromethorphan shows efficacy in experimental pain (nociception) and opioid tolerance

From the Pain Service, Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Supported in part by the VZV Foundation (K.J.E.) and NIDA grant DA01457 (C.E.I.).
Address correspondence and reprint requests to Dr Elliott, Memorial Sloan-Kettering Cancer Center, Department of Neurology, Pain Service, 1275 York Avenue, New York, NY 10021.

The oral antitussive dextromethorphan is a clinically available N-methyl-D-aspartate receptor antagonist. Dextromethorphan has analgesic efficacy in the experimental formalin test, blocks the nociceptive activation of the immediate-early gene, c-fos proto-oncogene, and prevents and reverses the development of opiate analgesic tolerance in experimental models. These data suggest that dextromethorphan should be evaluated in a controlled clinical trial for analgesic efficacy in zoster-associated neuralgia.

NEUROLOGY 1995;45(Suppl 8): S66-S68

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