Department of Genetic Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
J Ethnopharmacol. 2012 Jan 31;139(2):616-25. doi: 10.1016/j.jep.2011.12.003. Epub 2011 Dec 13.
Polygonum hydropiper L. (Polygonaceae) has been traditionally used to treat various inflammatory diseases such as rheumatoid arthritis. However, no systematic studies on the anti-inflammatory actions of Polygonum hydropiper and its inhibitory mechanisms have been reported. This study is therefore aimed at exploring the anti-inflammatory effects of 99% methanol extracts (Ph-ME) of this plant.
The effects of Ph-ME on the production of inflammatory mediators in RAW264.7 cells and peritoneal macrophages were investigated. Molecular mechanisms underlying the effects, especially inhibitory effects, were elucidated by analyzing the activation of transcription factors and their upstream signalling, and by evaluating the kinase activities of target enzymes. Additionally, a dextran sulphate sodium (DSS)-induced colitis model was employed to see whether this extract can be used as an orally available drug.
Ph-ME dose-dependently suppressed the release of nitric oxide (NO), tumour necrosis factor (TNF)-α, and prostaglandin (PG)E(2), in RAW264.7 cells and peritoneal macrophages stimulated by lipopolysaccharide (LPS). Ph-ME inhibited mRNA expression of pro-inflammatory genes such as inducible NO synthase (iNOS), cyclooxygenase (COX)-2, and TNF-α by suppressing the activation of nuclear factor (NF)-κB, activator protein (AP-1), and cAMP responsive element binding protein (CREB), and simultaneously inhibited its upstream inflammatory signalling cascades, including cascades involving Syk, Src, and IRAK1. Consistent with these findings, the extract strongly suppressed the kinase activities of Src and Syk. Based on HPLC analysis, quercetin, which inhibits NO and PGE(2) activities, was found as one of the active ingredients in Ph-ME.
Ph-ME exerts strong anti-inflammatory activity by suppressing Src/Syk/NF-κB and IRAK/AP-1/CREB pathways, which contribute to its major ethno-pharmacological role as an anti-gastritis remedy.
贯叶金丝桃(藤黄科)在传统医学中被用于治疗多种炎症性疾病,如类风湿性关节炎。然而,目前尚未有关于贯叶金丝桃抗炎作用及其抑制机制的系统研究。因此,本研究旨在探索该植物 99%甲醇提取物(Ph-ME)的抗炎作用。
研究了 Ph-ME 对 RAW264.7 细胞和腹腔巨噬细胞中炎症介质产生的影响。通过分析转录因子的激活及其上游信号,以及评估靶酶的激酶活性,阐明了其作用的分子机制,特别是抑制作用的机制。此外,还采用葡聚糖硫酸钠(DSS)诱导的结肠炎模型,观察该提取物是否可作为口服药物使用。
Ph-ME 呈剂量依赖性地抑制脂多糖(LPS)刺激的 RAW264.7 细胞和腹腔巨噬细胞中一氧化氮(NO)、肿瘤坏死因子(TNF)-α 和前列腺素(PG)E2 的释放。Ph-ME 通过抑制核因子(NF)-κB、激活蛋白(AP)-1 和 cAMP 反应元件结合蛋白(CREB)的激活,抑制促炎基因如诱导型一氧化氮合酶(iNOS)、环氧化酶(COX)-2 和 TNF-α 的 mRNA 表达,同时抑制其上游炎症信号级联反应,包括涉及 Syk、Src 和 IRAK1 的级联反应。与这些发现一致的是,该提取物强烈抑制 Src 和 Syk 的激酶活性。基于 HPLC 分析,发现抑制 NO 和 PGE2 活性的槲皮素是 Ph-ME 的一种活性成分。
Ph-ME 通过抑制 Src/Syk/NF-κB 和 IRAK/AP-1/CREB 通路发挥强大的抗炎作用,这有助于其作为抗胃炎药物的主要民族药理学作用。