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青蒿琥酯对类风湿关节炎滑膜细胞TNF-α分泌的抑制作用及其机制研究
引用本文:刘鹏,叶玉津,许韩师,杨岫岩,莫汉有,梁柳琴,陈少贞,江沁.青蒿琥酯对类风湿关节炎滑膜细胞TNF-α分泌的抑制作用及其机制研究[J].中国药物与临床,2007,7(7):520-523.
作者姓名:刘鹏  叶玉津  许韩师  杨岫岩  莫汉有  梁柳琴  陈少贞  江沁
作者单位:1. 510080,广州,中山大学附属第一医院康复医学科
2. 510080,广州,中山大学附属第一医院风湿免疫科
3. 桂林医学院附属医院血液风湿科
基金项目:广东省科技发展计划基金;广东省医药卫生科研项目
摘    要:目的研究青蒿素衍生物青蒿琥酯对类风湿关节炎(RA)滑膜细胞(FLS)分泌肿瘤坏死因子(TNF)-α的影响,并进一步探讨其机制。方法来自活动性RA患者的FLS用脂多糖(LPS)刺激和青蒿琥酯处理,TNF-α水平用酶联免疫吸附试验(ELISA)测定,核因子(NF)-κB活性检测采用电泳迁移率改变试验(EMSA)。结果青蒿琥酯显著抑制LPS诱导的TNF-α分泌,并且呈剂量依赖性。青蒿琥酯对LPS刺激的NF-κB活化有明显抑制作用,NF-κB抑制剂二硫代氨基吡咯烷(PDTC)亦显著抑制LPS刺激的滑膜细胞分泌TNF-α。结论青蒿琥酯通过调节NF-κB活性抑制LPS诱导的RA滑膜细胞分泌TNF-α,提示青蒿琥酯可能具有抑制RA滑膜炎症的作用。

关 键 词:细胞因子类  关节炎  类风湿  肿瘤坏死因子α
修稿时间:2007-04-13

Artesunate inhibits LPS-induced production of TNF-αvia inhibition of NF-κB signal pathway in human rheumatoid arthritis fibroblast-like synoviocytes
LIU Peng,YE Yu-jin,XU Han-shi,YA NG Xiu-yan,MO Han-you,LIANG Liu-qin,CHEN Shao-zhen,JIANG qin.Artesunate inhibits LPS-induced production of TNF-αvia inhibition of NF-κB signal pathway in human rheumatoid arthritis fibroblast-like synoviocytes[J].Chinese Remedies & Clinics,2007,7(7):520-523.
Authors:LIU Peng  YE Yu-jin  XU Han-shi  YA NG Xiu-yan  MO Han-you  LIANG Liu-qin  CHEN Shao-zhen  JIANG qin
Institution:Department of Rehabilitation Medicine, the First Affiliated Hospital, SUN Yat-sen University, Guangzhou 510080, China
Abstract:Objective Recent studies have indicate that the anti-malarial artemisinin and its derivatives may exert anti-inflammatory and immunomodulatory effects. In this study, we explored the effect of artesunate, a artemisinin derivative, on LPS-induced production of TNF-α in human rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS), and further investigated the signal mechanism by which this compound modulates the cytokine production. Methods RA FLS obtained from patients with active rheumatoid arthritis were stimulated with LPS and incubated with artesunate. TNF-α production was measured by ELISA and DNA-binding activity of NF-κB was measured by EMSA. Results Artesunate decreased the secretion of TNF-α from LPS-stimulated RA FLS in a dose-dependent manner, and also suppressed LPS-α-induced NF-κB DNA-binding activity. The production of TNF-α induced by LPS was decreased by PDTC, a chemical inhibitor of NF-κB. These observations suggest that artesunate inhibits production of TNF-α through inhibition of NF-κB signaling pathway. Conclusion Our results indicated that artesunate exert anti-inflammatory effect in RA FLS and provided evidence of artesunate as a potential treatment for RA.
Keywords:Cytokines  Arthritis  rheumatoid  Tumor necrosis factor-alpha
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