首页    期刊浏览 2024年11月23日 星期六
登录注册

文章基本信息

  • 标题:Inhibition of Nitric Oxide and Tumor Necrosis Factor-α (TNF-α) Production by Propenone Compound through Blockade of Nuclear Factor (NF)-κB Activation in Cultured Murine Macrophages
  • 本地全文:下载
  • 作者:Eung-Seok Lee ; Hye Kyung Ju ; Tae Churl Moon
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2004
  • 卷号:27
  • 期号:5
  • 页码:617-620
  • DOI:10.1248/bpb.27.617
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Lipopolysaccharide (LPS)-stimulated macrophages produce large amounts of nitric oxide (NO) by inducible nitric oxide synthase (iNOS). This is an important mechanism in macrophage-induced septic shock and inflammation. In the present study, we tested a synthetic propenone compound, 1-furan-2-yl-3-pyridin-2-yl-propenone (FPP-3) for its ability to inhibit the production of tumor necrosis factor-α (TNF-α) and an inducible enzyme, iNOS, in the LPS-stimulated murine macrophage-like cell line, RAW264.7. FPP-3 consistently inhibited nitric oxide (NO) and TNF-α production in a dose dependent manner, with IC50 values of 10.0 and 13.1 μ M , respectively. Western blotting probed with specific anti-iNOS antibodies showed that the decrease in quantity of the NO product was accompanied by a decrease in the iNOS protein level. In cells transiently transfected with nuclear factor (NF)-κB promoter-luciferase reporter construct, this compound clearly inhibited the LPS-stimulated NF-κB activation. Moreover, this compound inhibited IκB-α degradation in a concentration and time-dependent manner. These results indicate that FPP-3 inhibits NO production via inhibition of degradation of IκB-α through NF-κB activation.
  • 关键词:propenone compound;nitric oxide;inducible nitric oxide synthase;tumor necrosis factor-α (TNF-α);nuclear factor (NF)-κB
国家哲学社会科学文献中心版权所有