Kim Sun-Hee, Shin Kum-Joo, Kim Dohan, Kim Yun-Hee, Han Myoung-Sook, Lee Taehoon-G, Kim Euikyung, Ryu Sung-Ho, Suh Pann-Ghill
Department of Life Science, Division of Molecular and Life Science and School of Environmental Science and Engineering, Pohang University of Science and Technology, San 31 Hyojadong, Nam-Gu, Pohang, Kyungbuk 790-784, South Korea.
Biochem Pharmacol. 2003 Sep 15;66(6):955-63. doi: 10.1016/s0006-2952(03)00465-9.
Flavonoids are natural polyphenolic compounds that have anti-inflammatory, cytoprotective and anticarcinogenic effects. In this study, we investigated the effects of several flavonoids on nuclear factor-kappa B (NF-kappa B) activation by using luciferase reporter gene assay. Among the flavonoids examined, luteolin showed the most potent inhibition on lipopolysaccharide (LPS)-stimulated NF-kappa B transcriptional activity in Rat-1 fibroblasts. Luteolin did not inhibit either I kappa B alpha degradation or NF-kappa B nuclear translocation, DNA binding or phosphorylation by LPS. However, luteolin prevented LPS-stimulated interaction between the p65 subunit of NF-kappa B and the transcriptional coactivator CBP. In addition, a specific PKA inhibitor that blocked the phosphorylation of CREB and c-Jun by luteolin partially reversed the inhibitory effect of luteolin on NF-kappa B.CBP complex formation and NF-kappa B transcriptional activity by LPS. These data imply that inhibition of NF-kappa B transcriptional activity by luteolin may occur through competition with transcription factors for coactivator that is available in limited amounts. Taken together, this study provides a molecular basis for the understanding of the anti-inflammatory effects of luteolin.
黄酮类化合物是具有抗炎、细胞保护和抗癌作用的天然多酚类化合物。在本研究中,我们通过荧光素酶报告基因检测法研究了几种黄酮类化合物对核因子-κB(NF-κB)激活的影响。在所检测的黄酮类化合物中,木犀草素对大鼠1型成纤维细胞中脂多糖(LPS)刺激的NF-κB转录活性表现出最有效的抑制作用。木犀草素既不抑制IκBα降解,也不抑制NF-κB核转位、DNA结合或LPS诱导的磷酸化。然而,木犀草素可阻止LPS刺激的NF-κB p65亚基与转录共激活因子CBP之间的相互作用。此外,一种特异性PKA抑制剂可阻断木犀草素对CREB和c-Jun的磷酸化,该抑制剂可部分逆转木犀草素对LPS诱导的NF-κB.CBP复合物形成和NF-κB转录活性的抑制作用。这些数据表明,木犀草素对NF-κB转录活性的抑制可能是通过与转录因子竞争有限量的共激活因子而发生的。综上所述,本研究为理解木犀草素的抗炎作用提供了分子基础。