期刊文献+

藏紫草醇提物的抗炎作用及其机制 被引量:6

Anti-inflammatory effects and mechanism of Onosma hookeri ethanol extract
在线阅读 下载PDF
导出
摘要 目的研究藏紫草醇提物对脂多糖诱导的体内外炎症模型的作用及其机制。方法小鼠腹腔注射LPS建立急性腹膜炎模型,检测藏紫草醇提物对炎症因子水平的抑制作用。通过LPS诱导小鼠巨噬细胞RAW 264.7建立细胞炎症模型,检测藏紫草醇提取物对炎症介质和炎症因子的抑制作用,以及细胞中NF-κB通路相关蛋白(p65、p-IκBα、IκBα)的表达。结果藏紫草醇提物能降低小鼠腹腔灌洗液中及巨噬细胞上清液炎症因子的水平,抑制巨噬细胞中炎症介质iNOS和COX-2的表达及LPS诱导活化的NF-κB信号通路的活性。结论藏紫草醇提取物可能通过抑制NF-κB活化改善体内外炎症。 AIM To investigate the effect and mechanism of ethanol extract of Onosma hookeri Clarke.var.longiforum Duthie on LPS-induced inflammation models in vivo and in vitro.METHODS Mice injected intraperitoneally with LPS were developed into acute peritonitis models for detection of the effects of O.hookeri ethanol extract on inflammatory factors.The mouse macrophages RAW 264.7 were induced into cell inflammation models by LPS for investigation of effects of O.hookeri ethanol extract on inflammatory mediators and factors,in addition to the determination of expressions of NF-κB pathway-related proteins(p65,p-IκBα,IκBα)of cells.RESULTS O.hookeri ethanol extract reduced the levels of inflammatory factors in mouse peritoneal lavage fluid and macrophage supernatant fluid,and inhibited the expressions of iNOS and COX-2 and activity of LPS-induced NF-κB signaling pathway activation.CONCLUSION O.hookeri ethanol extract may improve the LPS-induced inflammation via inhibiting the activation of NF-κB.
作者 周子琪 刘益波 郭珊珊 索朗欧珠 ZHOU Zi-qi;LIU Yi-bo;GUO Shan-shan;Suolang-ouzhu(Tibet Vocational Technical College,Lhasa 850030,China)
出处 《中成药》 CAS CSCD 北大核心 2021年第11期3002-3007,共6页 Chinese Traditional Patent Medicine
基金 西藏自治区自然科学基金项目(XZ2017ZRG-111)。
关键词 藏紫草醇提物 RAW264.7 炎症 NF-ΚB ethanol extract of Onosma hookeri Clarke.var.longiforum Duthie RAW264.7 inflammation NF-κB
作者简介 周子琪(1986-),女,硕士,讲师,研究方向为园林植物与观赏园艺遗传育种。Tel:17397119765,E-mail:ziqizhou2011@163.com。
  • 相关文献

参考文献8

二级参考文献50

  • 1张玉梅,唐志红,夏敏,凌文华.花色苷对ApoE基因缺陷小鼠炎症信号转导的影响[J].营养学报,2005,27(3):249-252. 被引量:4
  • 2李晓瑾,谭秀芳,马媛,寇鑫辉.药用植物紫草的研究进展[J].新疆师范大学学报(自然科学版),2005,24(4):69-74. 被引量:15
  • 3廖晖,Linda K Banbury,David N Leach.12味止血中药对脂多糖诱导小鼠巨噬细胞产生一氧化氮的抑制作用[J].中国药房,2007,18(9):649-651. 被引量:28
  • 4Casserly I, Topol E. Convergence of atherosclerosis and Alzheimer's disease: inflammation, cholesterol, and misfolded proteins[J].Lancet, 2004, 363: 1139--1146.
  • 5Surh YJ, Chun KS, Cha HH, et aT. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals :down-regulation of COX-2 and iNOS through suppression of NF-kappa B activation[J]. Mutst Res, 2001, 480--481: 243--268.
  • 6Panaro MA, Brandonisio O, Acquafredda A, et al. Evidences for iNOS expression and nitric oxide production in the human macrophages [J]. Curr Drug Targets Immune Endocr Metab Disord, 2003, 3:210 --221.
  • 7Williams CS, Mann M, DuBois RN. The role of cyclooxygenases in inflammation, cancer, and development[J]. Oncogene, 1999,18: 7908--7916.
  • 8Haddad JJ, Land SC. Redox/ROS regulation of lipopolysaccharide-induced mitogen-activated protein kinase (MAPK) activation and MAPK-mediated TNF-alpha biosynthesis[J]. Br J Pharmacol,2002,135:520--536.
  • 9Hassan F, Islam S, Koide N, et al. Role of p38 mitogen-activated protein kinase (MAPK) for vacuole formation in lipopolysaccharide (LPS)-stimulated maerophages[J]. Microbiol Immunol, 2004,48: 807--815.
  • 10SuhHW, Choi SS, Lee JK, et al. Regulation of c-los and c-jun gene expression by lipopoly- saccharide and cytokines in primary cultured astrocytes: effect of PKA and PKC pathways[J]. Arch Pharm Res,2004,27: 396--401.

共引文献102

同被引文献155

引证文献6

二级引证文献17

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部