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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Flavonoids Identified from Korean Scutellaria baicalensis Georgi Inhibit Inflammatory Signaling by Suppressing Activation of NF-kappaB and MAPK in RAW 264.7 Cells
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Flavonoids Identified from Korean Scutellaria baicalensis Georgi Inhibit Inflammatory Signaling by Suppressing Activation of NF-kappaB and MAPK in RAW 264.7 Cells

机译:从韩国黄S中鉴定出的类黄酮通过抑制RAW 264.7细胞中NF-κB和MAPK的活化来抑制炎症信号

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摘要

Scutellaria baicalensis Georgi has been used as traditional medicine for treating inflammatory diseases, hepatitis, tumors, and diarrhea in Asia. Hence, we investigated the anti-inflammatory effect and determined the molecular mechanism of action of flavonoids isolated from Korean S. baicalensis G. in lipopolysaccharide- (LPS-) stimulated RAW 264.7 macrophages. A 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay was performed to examine cytotoxicity of the flavonoids at various concentrations of 10,40,70, and 100 mug/mL. No cytotoxicity was observed in RAW 264.7 cells at these concentrations. Furthermore, the flavonoids decreased production of inflammatory mediators such as inducible nitric oxide synthase, cyclooxygenase-2, interleukin-6, and tumor necrosis factor-alpha and inhibited phosphorylation of nuclear factor-kappa B (NF-kappaB) and mitogen-activated protein kinases (MAPKs) in LPS-induced RAW 264.7 cells. Moreover, to identify the differentially expressed proteins in RAW 264.7 cells of the control, LPS-treated, and flavonoid-treated groups, two-dimensional gel electrophoresis and mass spectrometry were conducted. The identified proteins were involved in the inflammatory response and included PRKA anchor protein and heat shock protein 70 kD. These findings suggest that the flavenoids isolated from S. baicalensis G. might have anti-inflammatory effects that regulate the expression of inflammatory mediators by inhibiting the NF-kappaB signaling pathway via the MAPK signaling pathway in RAW 264.7 cells.
机译:黄cut(Scutellaria baicalensis Georgi)已被用作治疗亚洲炎性疾病,肝炎,肿瘤和腹泻的传统药物。因此,我们研究了抗炎作用,并确定了从韩国黄ba中分离出的黄酮类化合物在脂多糖-(LPS-)刺激的RAW 264.7巨噬细胞中的分子作用机理。进行了3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物测定,以检查10、40、70和100杯/毫升各种浓度的类黄酮的细胞毒性。在这些浓度下,未在RAW 264.7细胞中观察到细胞毒性。此外,类黄酮减少了炎症介质的产生,例如诱导型一氧化氮合酶,环氧合酶-2,白介素-6和肿瘤坏死因子-α,并抑制了核因子-κB(NF-κB)和促分裂原活化蛋白激酶的磷酸化。 LPS诱导的RAW 264.7细胞中的(MAPKs)。此外,为鉴定对照组,LPS处理组和类黄酮处理组的RAW 264.7细胞中差异表达的蛋白质,进行了二维凝胶电泳和质谱分析。鉴定出的蛋白参与炎症反应,包括PRKA锚蛋白和热休克蛋白70 kD。这些发现表明,从黄ical中分离出的黄酮类化合物可能具有抗炎作用,通过抑制RAW 264.7细胞中经由MAPK信号传导途径的NF-κB信号传导途径来调节炎症介质的表达。

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