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Green Soybean Extract Ameliorates Dextran Sodium Sulfate-Induced Colitis

机译:绿豆提取物改善葡聚糖硫酸钠诱导的结肠炎

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Green-mature soybean (Glycine max) extract (GSE) inhibits the progression of immunoglobulin E-mediated inflammation more than the ordinary yellow-pigmented soybean extract (YSE). The inhibition of nitric oxide (NO) production by GSE in lipopolysaccharide-stimulated RAW264.7 cells has been found to be lower than that by YSE. However, this inhibitory ability became markedly pronounced by visible light irradiation. We investigated the anti-inflammatory effects of GSE and visible light-irradiated GSE (L-GSE) on dextran sodium sulfate (DSS)-induced colitis, immunoglobulin E-independent inflammation, and assessed whether light irradiation affects their anti-inflammatory properties. The severity of DSS-induced colitis was moderated by the ingestion of any of the soybean extracts, and L-GSE was the most effective in moderating the progression in colitis. GSE and L-GSE, except for YSE, inhibited the mRNA expressions of pro-inflammatory cytokines and chemokine in mice colons. All soybean extracts suppressed the mRNA expression of inducible nitric oxide synthase (iNOS), whereas GSE and L-GSE also inhibited the expression of the iNOS protein in the early phase of colitis. These results suggest that GSE is likely to suppress NO production, unlike in vitro results. Unfortunately, a significant difference in the anti-inflammation ability of GSE and L-GSE was not observed in the DSS-induced colitis mice. However, GSE and L-GSE are likely to become new candidate agents for the inhibition of inflammation and excessive NO production.
机译:绿色成熟大豆(甘氨酸Max)提取物(GSE)抑制免疫球蛋白E介导的炎症的进展,比普通的黄色着色的大豆提取物(yse)更高。已经发现通过GSE在脂多糖刺激的Raw264.7细胞中产生的一氧化氮(NO)产生的抑制性低于yse。然而,这种抑制能力通过可见光照射显着发音。我们调查了GSE和可见光辐照的GSE(L-GSE)对葡聚糖硫酸钠(DSS)的抗炎作用 - 诱导的结肠炎,免疫球蛋白E-无关的炎症,并评估了光辐射是否影响其抗炎性质。通过摄入任何大豆提取物,DSS诱导的结肠炎的严重程度受到调节,L-GSE是适度调节结肠炎的进展。除了YSE外,GSE和L-GSE抑制了小鼠冒号中促炎细胞因子和趋化因子的mRNA表达。所有大豆提取物都抑制了诱导型一氧化氮合酶(INOS)的mRNA表达,而GSE和L-GSE也抑制了在结肠炎早期癌症中InOS蛋白的表达。与体外结果不同,这些结果表明GSE可能会抑制不生产的生产。不幸的是,在DSS诱导的结肠炎小鼠中未观察到GSE和L-GSE的抗炎能力的显着差异。然而,GSE和L-GSE可能成为抑制炎症和过度生产的新候选药物。

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