Neuropathic pain sensations are differentially sensitive to dextrorphan

Neuroreport. 1994 Jul 21;5(12):1438-40. doi: 10.1097/00001756-199407000-00008.

Abstract

Rats with an experimental painful peripheral neuropathy (the CCI model) display heat-hyperalgesia and mechanoallodynia. Previous work has shown that the heat-hyperalgesia is suppressed by dextrorphan (DEX) and other N-methyl-D-aspartate (NMDA) receptor antagonists. The present work shows that when tested in the same rats, a dose of DEX that is maximally effective against heat-hyperalgesia has no effect on mechano-allodynia. The results suggest that different kinds of abnormal pain sensations may be caused by different pathophysiologic mechanisms that may respond differently to drug therapy.

MeSH terms

  • Animals
  • Dextrorphan / pharmacology*
  • Hot Temperature
  • Hyperalgesia / physiopathology
  • Male
  • Pain / physiopathology*
  • Peripheral Nervous System Diseases / physiopathology*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Sciatic Nerve / drug effects
  • Sciatic Nerve / physiology
  • Sciatic Nerve / physiopathology

Substances

  • Receptors, N-Methyl-D-Aspartate
  • Dextrorphan