期刊
AMERICAN JOURNAL OF CHINESE MEDICINE
卷 37, 期 1, 页码 181-194出版社
WORLD SCIENTIFIC PUBL CO PTE LTD
DOI: 10.1142/S0192415X0900676X
关键词
Paeonol; IL-6; NO; PGE(2); ERK
资金
- Wonkwang University
We evaluated the in vivo anti-inflammatory and analgesic activities of orally administered paeonol in mice, and also investigated the anti-inflammatory activity of paeonol in a cell line. Paeonol significantly reduced the edema induced by arachidonic acid in rats. The analgesic effects were assayed using 2 different models, i.e., by acetic acid-induced writhing response and by formalin induced licking and biting time. Moreover, we examined the effects of paeonol on the release of inflammatory mediators such as NO, PGE2 and IL-6. Our results demonstrated that paeonol inhibited LPS induced expression of NO, PGE2 and IL-6. Paeonol prevented LPS induced iNOS, COX-2 and ERK activation. Therefore, paeonol appears to have potential as a treatment for inflammatory disease and analgesic.
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