Mechanisms Involved in the Antinociceptive Effects of 7-Hydroxycoumarin
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文摘
7-Hydroxycoumarin (umbelliferone, <b>1b>), the main metabolite of coumarin, has been reported to produce potent antinociceptive effects in animal models of pain. However, the biochemical events involved in antinociception mediated by <b>1b> are currently not well understood. In the present study, the mechanisms by which <b>1b> exerts its pharmacological actions were investigated. Acute pretreatment of mice with <b>1b> produced a long-lasting antinociceptive effect against complete Freund鈥檚 adjuvant (CFA)-induced hyperalgesia. The subchronic administration of <b>1b> inhibited CFA-induced hyperalgesia and paw edema, while it did not cause any apparent toxicity. Another set of experiments showed that <b>1b> inhibited carrageenan-induced mechanical hyperalgesia, but not mechanical hyperalgesia induced by prostaglandin Eb>2b> (PGEb>2b>), suggesting that it acts upstream of PGEb>2.b> Treatment with <b>1b> was able to prevent the plantar tissue neutrophil influx induced by local inflammatory stimuli. In addition, <b>1b> exhibited inhibitory effects on the release of hyperalgesic cytokines (TNF-伪 and IL-1尾) and the production of PGEb>2b>, a directly acting hyperalgesic mediator. The present results suggest that the antinociceptive effect of <b>1b> is correlated with the inhibition of neutrophil migration, cytokine release, and PGEb>2b> production and are supportive of the further investigation of the therapeutic potential of <b>1b> to control inflammatory pain.

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