Effect of the low-affinity, noncompetitive N-methyl-d-aspartate receptor antagonist dextromethorphan on visceral perception in healthy volunteers

Aliment Pharmacol Ther. 2002 Nov;16(11):1955-62. doi: 10.1046/j.1365-2036.2002.01358.x.

Abstract

Background: The use of N-methyl-d-aspartate (NMDA) receptor antagonists may hold promise for the treatment of pain of visceral origin, in particular in conditions characterized by visceral hypersensitivity.

Aim: To study the effect of dextromethorphan, a low affinity, non-competitive NMDA receptor antagonist, on visceral perception in healthy volunteers.

Methods: Nine healthy volunteers (5 female, median age 22 years) underwent a gastric barostat study after oral administration of placebo, dextromethorphan 10 mg or dextromethorphan 30 mg, on three separate days in a double-blind, randomised order. Sensations induced by step-wise isobaric gastric distension (2 mmHg/2 min) were studied during fasting and 30 min after a meal. In addition, proximal gastric tone was measured during fasting and postprandially.

Results: Compared to placebo, dextromethorphan 30 mg significantly increased the distension-evoked sensation scores for nausea (P=0.004) and satiation (P=0.004) during fasting; and for bloating (P= 0.001), nausea (P=0.000) and satiation (P=0.01) 30 min postprandially. Dextromethorphan did not alter pain scores, proximal gastric tone or gastric compliance.

Conclusions: Dextromethorphan increases the perception of non-painful sensations during gastric distension, without altering the perception of pain. Therefore, application of dextromethorphan as a visceral analgesic is questionable. Future studies with more specific NMDA receptor antagonist are warranted.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Analgesics, Opioid / therapeutic use*
  • Dextromethorphan / therapeutic use*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Dyspepsia / etiology
  • Dyspepsia / prevention & control*
  • Fasting
  • Female
  • Gastric Dilatation
  • Humans
  • Hyperalgesia / etiology
  • Hyperalgesia / prevention & control*
  • Male
  • Postprandial Period
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
  • Stomach / drug effects*

Substances

  • Analgesics, Opioid
  • Receptors, N-Methyl-D-Aspartate
  • Dextromethorphan