
pmid: 17049512
The effects of methyleugenol, an essential oil isolated from Asiasari radix, on antinociception were examined using the formalin test in mice. Oral administration of 10 mg/kg methyleugenol significantly decreased the duration of licking and biting behavior in the second phase without affecting that of the first phase, as did diclofenac, a non-steroidal anti-inflammatory drug. Methyleugenol also inhibited pain-related behaviors induced by intrathecal injection of N-methyl-d-aspartic acid (NMDA), while diclofenac did not affect these behaviors. These effects of methyleugenol were suppressed by bicuculline, a gamma-aminobutyric acid(A) (GABA(A)) antagonist. Muscimol, a GABA(A) agonist, displays the same action as methyleugenol with respect to the formalin test and NMDA-induced behaviors. Methyleugenol did not affect cyclooxygenase-1 and -2 activities. These results suggest that the antinociceptive effect of methyleugenol on the second phase of formalin-induced pain may be due to the inhibition of NMDA receptor-mediated hyperalgesia via GABA(A) receptors.
Male, Diclofenac, N-Methylaspartate, Behavior, Animal, Muscimol, Anti-Inflammatory Agents, Non-Steroidal, Nociceptors, Mice, Cyclooxygenase 2, Hyperalgesia, Formaldehyde, Eugenol, Cyclooxygenase 1, Excitatory Amino Acid Agonists, Animals, GABA Agonists, Anesthetics
Male, Diclofenac, N-Methylaspartate, Behavior, Animal, Muscimol, Anti-Inflammatory Agents, Non-Steroidal, Nociceptors, Mice, Cyclooxygenase 2, Hyperalgesia, Formaldehyde, Eugenol, Cyclooxygenase 1, Excitatory Amino Acid Agonists, Animals, GABA Agonists, Anesthetics
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