植物源化合物菊内酯和绒毛蛋白对炎性细胞因子分泌的抑制作用:nf - κ b和STAT1的作用2010-02-10 2010-06-28 2010-08-12

Galya Abrham, S. Dovrat, H. Bessler, S. Grossman, U. Nir, M. Bergman
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引用次数: 20

摘要

植物粘菊已被证明具有许多重要的药用价值,包括抗炎、抗氧化、抗菌和抗真菌活性,但介导这些作用的植物代谢物及其作用机制尚不清楚。在之前的一项研究中,我们证明了用从粘菊叶中提取的纯化倍半萜内酯化合物Inuviscolide (Inv)和Tomentosin (Tom)处理黑色素瘤细胞中核因子κ B (NFB) p65亚基的表达降低。在这项研究中,我们测试了这些纯化的化合物在体外受脂多糖(LPS)或肉豆蔻酸酯(PMA)刺激时对人外周血单核细胞(pmcs)分泌促炎细胞因子的影响。并对其可能的作用机理进行了探讨。结果表明,两种药物均可导致IL-2、IL-1、IFN的产生降低,TNF的分泌略有增加,而IL-6的分泌不受影响。tnf水平升高似乎并不影响人类pbmc的生存能力。Western blot分析显示,核因子- B (NFB)的转录因子组分p65/RelA和转录信号换能器和激活因子1 (STAT1)的蛋白水平通过蛋白体降解而降低。然而,核因子- β组分p50 (NFB)或转录信号转导和激活因子3 (STAT3)的表达水平未见变化。综上所述,我们的研究结果表明,在细胞因子分泌过度刺激是病理症状基础的情况下,这些药物可能在未来被用作抗炎治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of Inflammatory Cytokine Secretion by Plant-Derived Compounds Inuviscolide and Tomentosin: The Role of NFκB and STAT1~!2010-02-10~!2010-06-28~!2010-08-12~!
The plant Inula viscosa has been shown to possess many important medicinal benefits, including anti-inflammatory, anti-oxidant, anti-bacterial, and anti-fungal activities, but the plant metabolites that mediate these effects and their mechanism of action are poorly understood. In a previous study, we demonstrated a reduced expression of the p65 subunit of nuclear factor kappa B (NFB) in melanoma cells treated with the purified sesquiterpene lactone compounds, Inuviscolide (Inv) and Tomentosin (Tom), extracted from Inula viscosa leaves. In this study, we tested the in- vitro effect of these purified compounds on the secretion of pro-inflammatory cytokines from human peripheral blood mononuclear cells (PBMCs) upon stimulation with lipopolysaccharide (LPS) or phorbol myristate acetate (PMA). Their possible mechanism of action was also studied. The results showed that both agents caused decreased production of IL-2, IL-1� , IFN� , and slightly increased secretion of TNF� , whereas secretion of IL-6 was not affected. The elevated levels of TNFdid not appear to affect the viability of human PBMCs. Western blot analysis revealed a reduction in the protein level of both the transcription factor component p65/RelA of nuclear factor-� B (NF B) and the signal transducer and activator of transcription 1 (STAT1) through proteosomal degradation. However, no change was observed in the expression level of the nuclear factor-� B component, p50 (NF B), or the signal transducer and activator of transcription 3 (STAT3). Taken together, our results indicate the possible future use of these agents as an anti-inflammatory treatment in cases where overstimulation of cytokine secretion is the basis for the pathological symptoms.
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