Shih Yu-Tzu, Wu Deng-Chyang, Liu Chi-Ming, Yang Yuan-Chieh, Chen Ing-Jun, Lo Yi-Ching
Department and Graduate Institute of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung City, Taiwan.
J Ethnopharmacol. 2007 Jul 25;112(3):537-44. doi: 10.1016/j.jep.2007.04.015. Epub 2007 Apr 27.
Helicobacter pylori infection leads to gastroduodenal inflammation, peptic ulceration, gastric lymphoma and gastric cancer. Certain herbal remedies have been used to treat gastric disease. In this study, we examined the anti-inflammatory effect of San-Huang-Xie-Xin-Tang (SHXT) and its main component baicalin on Helicobacter pylori-infected human gastric epithelial AGS cell. AGS cells were treated with Helicobacter pylori at a bacterium/cell ratio of 300:1. mRNA expression and protein levels were determined by reverse transcriptase-polymerase chain reaction (RT-PCR) analysis and western blot analysis, respectively. Interleukin-8 (IL-8) level and the translocation of nuclear factor kappa B (NF-kappaB) were measured by enzyme-linked immunosorbent assay (ELISA) and enzyme-linked DNA-protein interaction assay (ELDIA), respectively. Nitric oxide production was measured by Griess reagent. We found that SHXT and baicalin inhibited Helicobacter pylori-induced cyclooxygenase-2 (COX-2) enhancement and IkappaBalpha degradation in both mRNA and protein levels. SHXT and baicalin also inhibited Helicobacter pylori-induced inducible nitric oxide synthase (iNOS) and IL-8 mRNA expression, and decreased NO and IL-8 production. Furthermore, SHXT and baicalin inhibited nuclear translocation of p50 subunit of NF-kappaB in Helicobacter pylori-infected AGS cells. Based on the above findings, SHXT and baicalin might exert anti-inflammatory and gastroprotective effects in Helicobacter pylori-induced gastric inflammation.
幽门螺杆菌感染会导致胃十二指肠炎症、消化性溃疡、胃淋巴瘤和胃癌。某些草药疗法已被用于治疗胃部疾病。在本研究中,我们检测了三黄泻心汤(SHXT)及其主要成分黄芩苷对幽门螺杆菌感染的人胃上皮AGS细胞的抗炎作用。将AGS细胞与幽门螺杆菌以300:1的细菌/细胞比例进行处理。分别通过逆转录聚合酶链反应(RT-PCR)分析和蛋白质印迹分析来测定mRNA表达和蛋白质水平。分别通过酶联免疫吸附测定(ELISA)和酶联DNA-蛋白质相互作用测定(ELDIA)来测量白细胞介素-8(IL-8)水平和核因子κB(NF-κB)的易位。通过格里斯试剂测量一氧化氮的产生。我们发现,SHXT和黄芩苷在mRNA和蛋白质水平上均抑制幽门螺杆菌诱导的环氧化酶-2(COX-2)增强和IκBα降解。SHXT和黄芩苷还抑制幽门螺杆菌诱导的诱导型一氧化氮合酶(iNOS)和IL-8 mRNA表达,并降低NO和IL-8的产生。此外,SHXT和黄芩苷抑制幽门螺杆菌感染的AGS细胞中NF-κB p50亚基的核转位。基于上述发现,SHXT和黄芩苷可能在幽门螺杆菌诱导的胃炎症中发挥抗炎和胃保护作用。