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The quinoxaline derivative caroverine in the treatment of sensorineural smell disorders: a proof-of-concept study.

Abstract
The treatment of non-conductive olfactory disorders is to a large extent an unsolved problem. This proof-of-concept study focused on possible effects of the N-methyl-D-aspartate (NMDA) antagonist caroverine. Potential mechanisms for the hypothesized effect included reduced feedback inhibition in the olfactory bulb as a consequence of NMDA antagonistic actions and antagonism of an excitotoxic action of glutamate. A total of 77 consecutive patients with non-conductive olfactory disorders were included in the study. Fifty-one patients received caroverine for 4 weeks (120 mg/day); 26 controls matched for age, gender and duration of olfactory loss were treated with zinc sulfate for the same length of time (400 mg/day). Olfactory sensitivity was evaluated before and after treatment. Testing included assessment of n-butanol odor threshold and odor identification. When compared to baseline, treatment with caroverine improved both odor thresholds (p = 0.005) and odor identification (p = 0.042) in anosmic patients. In hyposmic patients it significantly improved odor identification ability (p = 0.041). In contrast, zinc sulfate had no significant effect on olfactory function. These results indicate that caroverine appears to be effective for the treatment of non-conductive smell disorders.
AuthorsChristian Quint, Andreas F P Temmel, Thomas Hummel, Klaus Ehrenberger
JournalActa oto-laryngologica (Acta Otolaryngol) Vol. 122 Issue 8 Pg. 877-81 (Dec 2002) ISSN: 0001-6489 [Print] England
PMID12542209 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Quinoxalines
  • N-Methylaspartate
  • Zinc Sulfate
  • caroverine
Topics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Humans
  • Male
  • Middle Aged
  • N-Methylaspartate (antagonists & inhibitors)
  • Olfaction Disorders (diagnosis, drug therapy, etiology)
  • Quinoxalines (therapeutic use)
  • Sensory Thresholds (drug effects)
  • Smell (drug effects)
  • Zinc Sulfate (therapeutic use)

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