Lin Qiu-Ye, Jin Li-Ji, Cao Zhen-Hui, Xu Yong-Ping
Department of Bioscience and Biotechnology, Dalian University of Technology, 2 Linggong Road, Ganjingzi District, Dalian, Liaoning 116024, People's Republic of China.
J Ethnopharmacol. 2008 Jul 23;118(2):231-6. doi: 10.1016/j.jep.2008.04.003. Epub 2008 Apr 11.
The herb Acanthopanax senticosus (Siberian ginseng) has long been used as a traditional medicine. However, little is known about anti-inflammatory effects and its mechanisms of action. Excess production of nitric oxide (NO) is one of the characteristics of inflammation. In this study we examined the effects of A. senticosus extract (ASE) on NO production and inducible nitric oxide synthase (iNOS) gene expression in lipopolysaccharide (LPS) plus interferon-gamma (IFN-gamma)-stimulated RAW264.7 macrophages and investigated its mechanisms of anti-inflammatory activity.
RAW264.7 macrophages were treated with 10 microg/ml LPS plus 20U/ml IFN-gamma in the presence or absence of ASE. NO production and iNOS gene expression were investigated. We further evaluated the effect of ASE on oxidative stress-sensitive transcription nuclear factor-kappa B (NF-kappaB) activation.
ASE significantly suppressed NO production and iNOS gene expression in a dose-dependent manner. ASE also reduced DNA-binding activity of NF-kappaB in LPS plus IFN-gamma stimulated RAW264.7 macrophages. Further studies indicated that LPS plus IFN-gamma-induced inhibitory factor-kappa B alpha (I-kappaBalpha) degradation and p65 nuclear translocation were inhibited in RAW264.7 macrophages exposed to ASE. Moreover, ASE inhibited the LPS plus IFN-gamma mediated increase in intracellular peroxides production.
These results suggest ASE suppresses iNOS gene expression through the inhibition of intracellular peroxides production, which has been implicated in the activation of NF-kappaB.
刺五加(西伯利亚人参)长期以来一直被用作传统药物。然而,关于其抗炎作用及其作用机制却知之甚少。一氧化氮(NO)的过量产生是炎症的特征之一。在本研究中,我们检测了刺五加提取物(ASE)对脂多糖(LPS)加干扰素-γ(IFN-γ)刺激的RAW264.7巨噬细胞中NO产生和诱导型一氧化氮合酶(iNOS)基因表达的影响,并研究了其抗炎活性机制。
在存在或不存在ASE的情况下,用10微克/毫升LPS加20单位/毫升IFN-γ处理RAW264.7巨噬细胞。检测NO产生和iNOS基因表达。我们进一步评估了ASE对氧化应激敏感转录核因子-κB(NF-κB)激活的影响。
ASE以剂量依赖的方式显著抑制NO产生和iNOS基因表达。ASE还降低了LPS加IFN-γ刺激的RAW264.7巨噬细胞中NF-κB的DNA结合活性。进一步研究表明,在暴露于ASE的RAW264.7巨噬细胞中,LPS加IFN-γ诱导的抑制因子-κBα(I-κBα)降解和p65核转位受到抑制。此外,ASE抑制了LPS加IFN-γ介导的细胞内过氧化物产生的增加。
这些结果表明,ASE通过抑制细胞内过氧化物的产生来抑制iNOS基因表达,而细胞内过氧化物的产生与NF-κB的激活有关。