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Dextrorphan and dextromethorphan attenuate glutamate neurotoxicity.

D. Choi

Brain Research February 17, 1987 DOI: 10.1016/0006-8993(87)90070-9 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics In vitro cell culture study Peer reviewed
Population Murine neocortical cell cultures
Interventions Dextrorphan Dextromethorphan
Dose 10-100 microM
Key points At 10-100 microM, dextrorphan attenuated morphological and chemical evidence of glutamate neurotoxicity in murine neocortical cell cultures, and dextromethorphan had a similar effect. The authors suggest these clinically tested opioids or related compounds may eventually prove useful therapeutically, given evidence that glutamate neurotoxicity may participate in neuronal loss in certain human neurological diseases.

Abstract

The dextrorotatory morphinan opioid, dextrorphan, which has recently been reported to block the excitation of cortical neurons by N-methyl-D-aspartate, was found at 10-100 microM concentrations to attenuate both morphological and chemical evidence of glutamate neurotoxicity in murine neocortical cell cultures; a similar effect was found with its methyl ester derivative, dextromethorphan. Given other data suggesting that glutamate neurotoxicity may participate in the pathogenesis of the central neuronal loss associated with certain human neurological diseases, the present observations raise the possibility that these clinically tested opioids, or related compounds, may eventually prove to have some clinical therapeutic utility.

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