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Salidroside의 RAW 264.7 세포에서 $NF{-kappa}B$ 불활성화를 통한 LPS에
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  • Salidroside의 RAW 264.7 세포에서 $NF{-kappa}B$ 불활성화를 통한 LPS에
  • Inhibition of LPS induced iNOS, COX-2 and cytokines expression by salidroside through the $NF{-kappa}B$ inactivation in RAW 264.7 cells
저자명
원소정,박희준,이경태,Won. So-Jung,Park. Hee-Juhn,Lee. Kyung-Tae
간행물명
생약학회지
권/호정보
2008년|39권 2호|pp.110-117 (8 pages)
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한국생약학회
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

In this study, we investigated the anti-inflammatory effects of salidroside (SAL) isolated from the MeOH extract of Acer tegmentosum Maxim heartwood in RAW 264.7 macrophage cells. SAL pretreatment significantly inhibited nitric oxide (NO) and prostaglandin $E_2$ ($PGE_2$) productions in the lipopolysaccharide (LPS)-induced RAW 264.7 cells. Western blot and RT-PCR analyses revealed that SAL inhibited the LPS-induced expressions of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the protein and mRNA levels in a concentration-dependent manner. In addition, SAL reduced the release and the mRNA expressions of tumor necrosis $factor-{alpha}$ ($TNF-{alpha}$) and interleukin-6 (IL-6). Furthermore, nuclear factorkappa B ($NF{-kappa}B$) luciferase reporter assay was performed to know the involvement of SAL in the production of pro-inflammatory cytokines, we confirmed that LPS-induced transcription activity of $NF{-kappa}B$ was inhibited by SAL. Taken together, our data indicate that anti-inflammatory property of salidroside might be the result from the inhibition of iNOS, COX-2, $TNF-{alpha}$ and IL-6 expressions via the down-regulation of $NF{-kappa}B$ activity.