Anti-inflammatory Activities of an Ethanol Extract of Ecklonia stolonifera in Lipopolysaccharide-Stimulated RAW 264.7 Murine Macrophage Cells

作者:Lee Min Sup; Kwon Mi Sung; Choi Ji Woong; Shin Taisun; No Hong Kyoon; Choi Jae Sue; Byun Dae Seok; Kim Jae Il; Kim Hyeung Rak*
来源:Journal of Agricultural and Food Chemistry, 2012, 60(36): 9120-9129.
DOI:10.1021/jf3022018

摘要

Ecklonia stolonifera is a brown alga that was shown to have antioxidant, anti-inflammatory, tyrosinase inhibitory, and chemopreventive activities. However, the molecular mechanisms underlying its anti-inflammatory activity remain unclear. In this study, we investigated the molecular mechanism of the anti-inflammatory action of E. stolonifera ethanolic extracts (ESE) using lipopolysaccharide (LPS)-stimulated RkW 264.7 cells. ESE inhibited LPS-induced nitric oxide (IC50 = 72 +/- 1.9 mu g/mL) and prostaglandin E-2 (IC50 = 98 +/- 5.3 mu g/mL) production in a dose-dependent manner and suppressed the expression of inducible nitric oxide synthase and cyclooxygenase-2 in RAW 264.7 cells. ESE also reduced the production of pro-inflammatory cytokines in LPS-stimulated RAW 264.7 cells. LPS-induced nuclear factor-kappa B (NF-kappa B) transcriptional activity and NF-kappa B translocation into the nucleus were significantly inhibited by ESE treatment through the prevention of the degradation of inhibitor kappa B-alpha. Moreover, ESE inhibited the activation of Akt, ERK, JNK1/2, and p38 MAPK in LPS-stimulated RAW 264.7 cells. The main components with anti-inflammatory activity in ESE were identified as phlorofucofuroeckol A and B based on the inhibition of NO production. Our results indicate that ESE can be considered as a potential source of therapeutic agents for inflammatory diseases.

  • 出版日期2012-9-12