Li Hai-Long, Chen Hai-Long, Li Hong, Zhang Kai-Li, Chen Xiao-Yan, Wang Xiao-Wei, Kong Qing-You, Liu Jia
Department of Surgery, The First Affiliated Hospital, Dalian Medical University, Dalian, PR China.
Int J Mol Med. 2005 Jul;16(1):41-7.
Emodin, an anthraquinones component of Rheum palmatun, has been used for anti-inflammatory purposes. However, its underlying molecular effect(s) on target cells remain to be well clarified. Thus, our current study was aimed at investigating the regulatory mechanism of emodin on liposaccharide-induced inflammatory responses in RAW 264.7 macrophages by RT-PCR, Western blot analysis, immunocytochemical staining and immunofluorescence analysis. It was found that a treatment of 20 microg/ml emodin inhibited the expression of a panel of inflammatory-associated genes, including TNFalpha, iNOS, IL-10, cytosolic IkappaBalpha, IKK-alpha and IKK-gamma, to different extents as well as the nuclear translocation of NF-kappaB (nuclear factor-kappaB). The promoting effect of emodin on the production and translocation of p105 (the precursor of NF-kappaB p50) was time-dependent and reached a maximum at 5 h. Our data suggest that emodin plays its anti-inflammatory roles by regulating inflammatory cytokines, specifically by suppressing NF-kappaB activation.
大黄素是掌叶大黄的一种蒽醌类成分,已被用于抗炎目的。然而,其对靶细胞潜在的分子作用仍有待充分阐明。因此,我们当前的研究旨在通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹分析、免疫细胞化学染色和免疫荧光分析,研究大黄素对脂多糖诱导的RAW 264.7巨噬细胞炎症反应的调控机制。研究发现,20微克/毫升大黄素处理不同程度地抑制了一组炎症相关基因的表达,包括肿瘤坏死因子α(TNFα)、诱导型一氧化氮合酶(iNOS)、白细胞介素10(IL-10)、胞质IκBα、IκB激酶α(IKK-α)和IκB激酶γ(IKK-γ),以及核因子κB(NF-κB)的核转位。大黄素对p105(NF-κB p50的前体)产生和转位的促进作用具有时间依赖性,在5小时时达到最大值。我们的数据表明,大黄素通过调节炎症细胞因子发挥其抗炎作用,特别是通过抑制NF-κB激活。