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Suppression of lipopolysaccharide-induced of inducible nitric oxide synthase and cyclooxygenase-2 by Sanguis Draconis, a dragon's blood resin, in RAW 264.7 cells
Authors:Choy Cheuk-Sing  Hu Chien-Ming  Chiu Wen-Ta  Lam Carlos-Shu Kei  Ting Yih  Tsai Shin-Han  Wang Tzu-Chien
Affiliation:Emergency Department of Municipal Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, ROC.
Abstract:Sanguis Draconis (SD) is a kind of dragon's blood resin that is obtained from Daemomorops draco (Palmae). It is used in traditional medicine and has shown anti-inflammatory activity in some diseases. In this study, we examined the effects of Sanguis Dranonis ethanol extract (SDEE) on LPS-induced inflammation using RAW 264.7 cells. Our data indicated that SDEE inhibits LPS-stimulated NO, PGE2, IL-1 beta and TNF-alpha release, and iNOS and COX-2 expression. Furthermore, SDEE suppressed the LPS-induced p65 expression of NF-kappa B, which was associated with the inhibition of I kappa B-alpha degradation. We also found that the expression of HO-1 was significantly increased in RAW 264.7 cells by SDEE. These results suggest among possibilities of anti-inflammation that SDEE inhibits the production of NO and PGE2 by the down-regulation of iNOS and COX-2 gene expression via the suppression of NF-kappaB (p65) activation. SDEE can induce HO-1 over-expression in macrophage cells, which indicates that it may possess antioxidant properties. This result means that SEDD its anti-inflammatory effects in macrophages may be through a novel mechanism that involves the action of HO-1. Thus, SD could provide a potential therapeutic approach for inflammation-associated disorders.
Keywords:COX-2, cyclooxygenase-2   eNOS, endothelial nitric oxide synthase   HO-1, heme oxgenase-1   IκB-α, inhibitory factor κB-α   IL-1β, interlukin-1β   iNOS, inducible nitric oxide synthase   LPS, lipopolysaccharide   NF-κB, nuclear factor-κB   NO, nitric oxide   nNOS, neuronal nitric oxide synthase   PGE2, prostaglandin E2   SD, Sanguis Draconis   SDEE, Sanguis Draconis ethanol extract   TNF-α, tumor necrosis factor-α
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