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Antioxidant and anti-inflammatory effects of an ethanol fraction from the Schisandra chinensis baillon hot water extract fermented using Lactobacilius paracasei subsp. tolerans

机译:用副干酪乳杆菌亚种发酵的五味子五味子热水提取物中的乙醇馏分的抗氧化和抗炎作用。宽容

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摘要

Effects of RPG-OM-30E on NO production in LPS-stimulated RAW 264.7 cells. ( ) Scheme for fraction of RPG-OM-30E from byproduct. ( ) LPS-stimulated RAW 264.7 cells were used for testing the inhibition of NO production. Inhibitory effects of fermented and unfermented hot water extract on NO production were compared in the concentration of 5 and 10%. ( ) The inhibition of NO production by ethanol fractions of fermented hot water extract was tested at the concentration of 0.1 mg/mL. ( ) Cell viability was determined through the WST assay. Cells were treated with each concentration of RPG-OM-30E for 24 h. Values are expressed as percentages of the control (0.1% DMSO). ( ) The effects of RPG-OM-30E on LPS-induced NO production were measured using the Griess reagent. Cells were stimulated with 1 μg/mL of LPS in the presence of each concentration of RPG-OM-30E. NO production was measured after 24 h. Significant compared to the group treated with LPS alone, * p p
机译:RPG-OM-30E对LPS刺激的RAW 264.7细胞中NO产生的影响。 ()从副产物中分离RPG-OM-30E的方案。 ()LPS刺激的RAW 264.7细胞用于测试NO产生的抑制。比较了浓度为5%和10%的发酵和未发酵热水提取物对NO产生的抑制作用。 ()在0.1 mg / mL的浓度下测试了乙醇成分对发酵热水提取物对NO产生的抑制作用。 ()通过WST测定法确定细胞活力。用每种浓度的RPG-OM-30E处理细胞24小时。值表示为对照(0.1%DMSO)的百分比。 ()使用Griess试剂测量RPG-OM-30E对LPS诱导的NO产生的影响。在每种浓度的RPG-OM-30E存在下,以1μg/ mL的LPS刺激细胞。 24小时后未测量到产量。与仅接受LPS治疗的组相比具有显着性,* p p

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