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Related Experiment Videos

Neurotoxicity of dextrorphan.

G G Ortiz1, J M Guerrero, R J Reiter

  • 1Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio, USA. orve@foreigner.class.udg.mx

Archives of Medical Research
|June 18, 1999
PubMed
Summary

Dextrorphan, a low-affinity NMDA antagonist, causes neurotoxicity in rats, similar to high-affinity antagonists. This study evaluated dextrorphan

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Area of Science:

  • Neuroscience
  • Pharmacology

Background:

  • Noncompetitive NMDA antagonists like phencyclidine (PCP) and dizocilpine (MK-801) show neuroprotective potential but cause neuronal injury.
  • Dextrorphan, a low-affinity NMDA antagonist, is also considered for neuroprotection.

Purpose of the Study:

  • To evaluate the neurotoxic effects of dextrorphan.

Main Methods:

  • Male Sprague-Dawley rats received intraperitoneal injections of saline or dextrorphan (30 mg/kg).
  • Brains were examined for histopathological changes 30 minutes post-injection.

Main Results:

  • Dextrorphan administration resulted in hyperchromatic, shrunken nuclei with chromatin condensation and disruption.
  • Pyramidal neurons in the retrosplenial cortex exhibited granular and vacuolated cytoplasm.

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  • Status spongiosus (spongy degeneration) of the neuropil was observed.
  • Conclusions:

    • The observed morphological changes in neurons are consistent with those induced by high-affinity NMDA antagonists.
    • Dextrorphan exhibits neurotoxic properties, similar to other noncompetitive NMDA antagonists.