Wun Zih-Yi, Lin Chwan-Fwu, Huang Wen-Chung, Huang Yu-Ling, Xu Pei-Yin, Chang Wei-Tien, Wu Shu-Ju, Liou Chian-Jiun
Department of Nutrition and Health Sciences, Chang Gung University of Science and Technology, 261 Wen-Hwa 1st Road, Kwei-Shan, Tao-Yuan 333, Taiwan, ROC.
Food Chem Toxicol. 2013 Dec;62:255-61. doi: 10.1016/j.fct.2013.08.072. Epub 2013 Sep 2.
Sophoraflavanone G (SG; 5,7,D, 2',4'-tetrahydroxy-8-lavandulylflavanone) has been isolated from Sophora flavescens and found to be effective against bacteria and to decrease cyclooxygenase (COX)-2 expression in RAW 264.7 macrophage. However, the anti-inflammatory mechanisms of SG are not well understood. RAW 264.7 cells were pretreated with various concentrations of SG (2.5-20 μM) and inflammatory responses were induced with lipopolysaccharide. Using enzyme-linked immunosorbent assay, the levels of pro-inflammatory cytokines and prostaglandin E2 (PGE2) were determined. Western blot was used to examine the protein expression of inducible nitric oxide synthase (iNOS), COX-2, and heme oxygenase-1 (HO-1). To investigate the molecular mechanism, we analyzed inflammatory-associated signaling pathways, including nuclear transcription factor kappa-B (NF-κB) and mitogen-activated protein kinase (MAPK). SG inhibited the levels of nitric oxide and PGE2 and decreased the production of pro-inflammatory cytokines, such as interleukin (IL)-1β, IL-6, and tumor necrosis factor α. The expression of iNOS and COX-2 was also suppressed. However, SG increased HO-1 production in a concentration-dependent manner and significantly decreased MAPK activation and inhibited NF-κB subunit p65 proteins to translocate into the nucleus. These results suggest that SG has an anti-inflammatory effect, inhibiting pro-inflammatory cytokines and mediators production via interruption of the NF-κB and MAPK signaling pathways.
槐黄酮G(SG;5,7,二羟基,2',4'-四羟基-8-薰衣草基黄酮)已从苦参中分离出来,发现其对细菌有效,并能降低RAW 264.7巨噬细胞中环氧化酶(COX)-2的表达。然而,SG的抗炎机制尚不完全清楚。用不同浓度的SG(2.5-20μM)预处理RAW 264.7细胞,并用脂多糖诱导炎症反应。采用酶联免疫吸附测定法测定促炎细胞因子和前列腺素E2(PGE2)的水平。用蛋白质印迹法检测诱导型一氧化氮合酶(iNOS)、COX-2和血红素加氧酶-1(HO-1)的蛋白表达。为了研究分子机制,我们分析了炎症相关信号通路,包括核转录因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)。SG抑制一氧化氮和PGE2水平,减少促炎细胞因子如白细胞介素(IL)-1β、IL-6和肿瘤坏死因子α的产生。iNOS和COX-2的表达也受到抑制。然而,SG以浓度依赖性方式增加HO-1的产生,并显著降低MAPK激活,抑制NF-κB亚基p65蛋白转位到细胞核。这些结果表明,SG具有抗炎作用,通过中断NF-κB和MAPK信号通路抑制促炎细胞因子和介质的产生。