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In-vitro and in-vivo anti-inflammatory effect of oxyresveratrol from Morus alba L.

机译:桑白皮中氧白藜芦醇的体内和体外抗炎作用

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摘要

The antioxidative effects of mulberroside A and oxyresveratrol obtained from Mori Cortex were examined. Mulberroside A and oxyresveratrol showed an inhibitory effect against FeSO4/H2O2-induced lipid peroxidation in rat microsomes and a scavenging effect on 1,1-diphenyl-2-picrylhydrazyl radical. The anti-inflammatory effects of mulberroside A and oxyresveratrol using the carrageenin-induced model of inflammation were investigated in rats. Mulberroside A and oxyresveratrol significantly reduced paw edema. To investigate the mechanism of the anti-inflammatory action of these compounds, we examined the effects of oxyresveratrol on lipopolysaccharide (LPS)-induced responses in murine macrophage cell line RAW 264.7. Exposure of LPS-stimulated cells to oxyresveratrol inhibited nitrite accumulation in the culture medium. Oxyresveratrol also inhibited the LPS-stimulated increase of inducible nitric oxide synthase (iNOS) expression in a concentration-dependent manner; however, it had little effect on iNOS enzymeactivity, suggesting that the inhibitory activity of oxyresveratrol is mainly due to the inhibition of iNOS expression rather than iNOS enzyme activity. Oxyresveratrol significantly inhibited LPS-evoked nuclear translocation of NF-kappaB and cyclooxygenase-2 (COX-2) activity in RAW 264.7 cells. The results suggest that the anti-inflammatory properties of oxyresveratrol might be correlated with inhibition of the iNOS expression through down-regulation of NF-kappaB binding activity and significant inhibition of COX-2 activity.
机译:研究了从Mori Cortex获得的桑树苷A和氧白藜芦醇的抗氧化作用。 Mulberroside A和氧白藜芦醇对FeSO4 / H2O2诱导的大鼠微粒体脂质过氧化具有抑制作用,并且对1,1-二苯基-2-picylhydrazyl自由基具有清除作用。在大鼠中研究了角叉菜胶诱导的炎症模型对桑树苷A和氧白藜芦醇的抗炎作用。 Mulberroside A和氧白藜芦醇可显着减轻爪水肿。为了研究这些化合物的抗炎作用的机制,我们检查了氧化白藜芦醇对脂多糖(LPS)诱导的鼠巨噬细胞RAW 264.7细胞应答的影响。 LPS刺激的细胞暴露于氧白藜芦醇可抑制培养基中亚硝酸盐的积累。乙醛白藜芦醇还以浓度依赖的方式抑制LPS刺激的诱导型一氧化氮合酶(iNOS)表达的增加;但是,它对iNOS酶的活性影响很小,这表明氧白藜芦醇的抑制活性主要是由于iNOS表达的抑制而不是iNOS酶的活性。乙醛白藜芦醇显着抑制RAW 264.7细胞中LPS诱发的NF-κB核转运和环氧合酶2(COX-2)活性。结果表明,氧白藜芦醇的抗炎特性可能与通过下调NF-κB结合活性和显着抑制COX-2活性抑制iNOS表达有关。

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