Kim Y W, Zhao R J, Park S J, Lee J R, Cho I J, Yang C H, Kim S G, Kim S C
Innovative Drug Research Center for Metabolic and Inflammatory Disease, College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Korea.
Br J Pharmacol. 2008 May;154(1):165-73. doi: 10.1038/bjp.2008.79. Epub 2008 Mar 10.
Glycyrrhizae radix has been widely used as a cytoprotective, plant-derived medicine. We have identified a flavanoid, liquiritigenin, as an active component in extracts of Glycyrrhizae radix. This research investigated the effects of liquiritigenin on the induction of inducible NOS (iNOS) and proinflammatory cytokines by lipopolysaccharide (LPS) in Raw264.7 cells, and on paw oedema in rats.
iNOS expression was determined by western blotting, real-time reverse transcription-PCR and reporter gene analyses. Tumour necrosis factor-alpha (TNF-alpha), interleukin (IL)-1beta and IL-6 were assayed by ELISA. Gel shift assay and immunoblotting were used to assess NF-kappaB activation. The effect of liquiritigenin on acute inflammation in vivo was evaluated using carrageenan-induced paw oedema.
Treatment of Raw264.7 cells with liquiritigenin caused inhibition of LPS-induced NF-kappaB DNA binding activity, due to repression of I-kappaBalpha phosphorylation and degradation. Liquiritigenin treatment prevented LPS from increasing the levels of iNOS protein and mRNA in a concentration-dependent manner. Liquiritigenin also suppressed the production of TNF-alpha, IL-1beta and IL-6 from Raw264.7 cells after LPS. In rats, liquiritigenin treatment inhibited formation of paw oedema induced by carrageenan.
These results demonstrate that liquiritigenin exerts anti-inflammatory effects, which results from the inhibition of NF-kappaB activation in macrophages, thereby decreasing production of iNOS and proinflammatory cytokines. Our findings showing inhibition by liquiritigenin of paw oedema as well as inflammatory gene induction will help to understand the pharmacology and mode of action of liquiritigenin, and of the anti-inflammatory use of Glycyrrhizae radix.
甘草根已被广泛用作一种具有细胞保护作用的植物源药物。我们已鉴定出一种黄酮类化合物,即甘草素,为甘草根提取物中的活性成分。本研究调查了甘草素对脂多糖(LPS)诱导Raw264.7细胞中诱导型一氧化氮合酶(iNOS)和促炎细胞因子的影响,以及对大鼠足爪水肿的影响。
通过蛋白质免疫印迹法、实时逆转录 - 聚合酶链反应和报告基因分析来测定iNOS的表达。采用酶联免疫吸附测定法检测肿瘤坏死因子 -α(TNF -α)、白细胞介素(IL)-1β和IL -6。凝胶迁移试验和免疫印迹法用于评估核因子 -κB(NF -κB)的激活情况。使用角叉菜胶诱导的足爪水肿来评估甘草素对体内急性炎症的作用。
用甘草素处理Raw264.7细胞可抑制LPS诱导的NF -κB DNA结合活性,这是由于I -κBα磷酸化和降解受到抑制。甘草素处理以浓度依赖的方式阻止LPS增加iNOS蛋白和mRNA的水平。甘草素还抑制了LPS刺激后Raw264.7细胞中TNF -α、IL -1β和IL -6的产生。在大鼠中,甘草素处理可抑制角叉菜胶诱导的足爪水肿形成。
这些结果表明,甘草素发挥抗炎作用,其机制是抑制巨噬细胞中NF -κB的激活,从而减少iNOS和促炎细胞因子的产生。我们的研究结果表明甘草素可抑制足爪水肿以及炎症基因的诱导,这将有助于理解甘草素的药理学特性和作用模式,以及甘草根的抗炎用途。