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中国临床药理学与治疗学 ›› 2011, Vol. 16 ›› Issue (6): 611-616.

• 基础研究 • 上一篇    下一篇

黄芪注射液对脂多糖诱导的内皮细胞炎症因子产生的影响及其机制研究

梁荣寿, 李健哲   

  1. 广西中医学院附属瑞康医院药剂科,南宁 530011,广西
  • 收稿日期:2010-12-23 修回日期:2011-05-26 发布日期:2011-07-25
  • 通讯作者: 李健哲,男,博士研究生,研究方向:心血管药理学。 Tel: 13659614937 E-mail: lijianzhe20035@126.com
  • 作者简介:梁荣寿,男,主管药师,研究方向:心血管药理学。 Tel: 13877123997 E-mail: rongshouliang0771@126.com

Effect and mechanism of radix astragali injection on production of inflammatory factors induced by lipopolysaccharide in human umbilical vein endothelial cells

LIANG Rong-shou, LI Jian-zhe   

  1. Department of Pharmacy, Ruikang Hospital, Guangxi College of Traditional Chinese Medicine, Nanning 530011, Guangxi, China
  • Received:2010-12-23 Revised:2011-05-26 Published:2011-07-25

摘要: 目的: 观察黄芪注射液对脂多糖(LPS)诱导的内皮细胞炎症因子产生的影响,并初步探讨黄芪注射液的抗炎作用机制。方法: 体外培养的人脐静脉内皮细胞(HUVECs),待细胞生长到融合状态时加入不同浓度(10、20、40 mg/L)的黄芪注射液预处理2 h,然后加入LPS(1 mg/L)作用24 h。用四唑盐比色实验(MTT)检测细胞活力;半定量逆转录-聚合酶链式反应(RT-PCR)和酶联免疫吸附法(ELISA)分别检测内皮细胞细胞间黏附分子-1(ICAM-1)、白介素-8(IL-8)和肿瘤坏死因子-α(TNF-α)mRNA的表达和其在上清液中的含量;实时荧光定量PCR(real-time PCR)检测Toll样受体4(TLR4) mRNA的表达;凝胶电泳迁移率实验(EMSA)检测NF-κB活性。结果: LPS能明显降低细胞活力,并能显著增加ICAM-1、IL-8和TNF-α mRNA的表达和含量,同时TLR4 mRNA的表达和NF-κB的活性也显著升高,而预先应用不同浓度的黄芪注射液处理后,上述效应明显减弱。结论: 黄芪注射液抑制炎症因子的产生可能与其抑制TLR-4/NF-κB信号通路有关。

关键词: 黄芪注射液, 脂多糖, 内皮细胞, Toll样受体4, 核因子-κB, 炎症因子

Abstract: AIM: To observe the effect of radix astragali injection on the production of inflammatory factors induced by lipopolysaccharide (LPS) and investigate the anti-inflammation mechanism of radix astragali injection. METHODS: The human umbilical vein endothelial cells (HUVECs) were treated with LPS (1 mg/L) for 24 h following pretreatment with various concentrations of radix astragali injection (10, 20 or 40 mg/L) for 2 h. Cell viability was detected by MTT; The mRNA expression and levels of intercellular adhesion molecule-1 (ICAM-1), interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α) were determinded by reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA) respectively; The mRNA expression of Toll-like receptor 4 (TLR4) was measured by real-time quantitative reverse transcription-polymerase chain reaction (real-time RT-PCR) and the activity of nuclear factor kappa B (NF-κB) was assayed by electrotracellular mobility shift assay (EMSA). RESULTS: LPS could significantly decrease the cell viability, increase the mRNA expression and levels of ICAM-1, IL-8 and TNF-α, upregulate the expression of TLR4 mRNA and NF-κB acitivity. However, the aboving effects of LPS were markedly inhibited by pretreatment with radix astragali injection. CONCLUSION: Radix astragali injection inhibits the production of inflammatory factors may be associated with depressing the TLR4/ NF-κB signaling pathway.

Key words: Radix astragali injection, Lipopolysaccharide, Endothelial cell, Toll-like receptors 4, Nuclear factor-κB, Inflammatory factor

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