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Inhibitory effect of sulphated polysaccharide porphyran on nitric oxide production in lipopolysaccharide-stimulated RAW264.7 macrophages

机译:硫酸多糖卟啉对脂多糖刺激的RAW264.7巨噬细胞中一氧化氮产生的抑制作用

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Porphyran, extracted from an edible red alga (Porphyra yezoensis), is a sulphated polysaccharide with a wide variety of biological activities including anti-tumour, antioxidant and immuno-modulating activities. In this study, we examined the effect of porphyran on nitric oxide (NO) production in mouse macrophage cell line RAW264.7 cells. Although no significant activity of porphyran to induce NO or tumour necrosis factor-α (TNF-α) production in RAW264.7 cells was observed at the concentration range tested (10–500 µg/ml), it was found for the first time that porphyran inhibited NO production and expression of inducible nitric oxide synthase (iNOS) in RAW264.7 cells stimulated with lipopolysaccharide (LPS). In the presence of 500 µg/ml porphyran, NO production and expression of iNOS in LPS-treated RAW264.7 cells were completely suppressed. On the other hand, porphyran showed only a marginal effect on the secretion of TNF-α from LPS-stimulated RAW264.7 cells. Electrophoretic mobility shift assay (EMSA) using infrared dye labelled oligonucleotide with nuclear factor-κB (NF-κB) consensus sequence suggested that porphyran inhibited the LPS-induced NF-κB activation. The LPS-inducible nuclear translocation of p65, and the phosphorylation and degradation of IκB-α were also inhibited by the pre-treatment with porphyran. Our results obtained in in vitro analysis suggest that porphyran suppresses NO production in LPS-stimulated macrophages by the blocking of NF-κB activation.
机译:紫菜提取自可食用的红藻(Porphyra yezoensis),是一种硫酸化多糖,具有多种生物活性,包括抗肿瘤,抗氧化剂和免疫调节活性。在这项研究中,我们检查了卟啉对小鼠巨噬细胞RAW264.7细胞中一氧化氮(NO)产生的影响。尽管在所测试的浓度范围(10–500 µg / ml)下未观察到卟啉在RAW264.7细胞中诱导NO或肿瘤坏死因子-α(TNF-α)产生的显着活性,但首次发现卟啉抑制了脂多糖(LPS)刺激的RAW264.7细胞中NO的产生和诱导型一氧化氮合酶(iNOS)的表达。在500 µg / ml的卟啉存在下,LPS处理的RAW264.7细胞中NO的产生和iNOS的表达被完全抑制。另一方面,卟啉对LPS刺激的RAW264.7细胞的TNF-α分泌仅显示出少量作用。使用具有核因子-κB(NF-κB)共有序列的红外染料标记的寡核苷酸进行的电泳迁移率迁移分析(EMSA)表明,卟啉可抑制LPS诱导的NF-κB活化。卟啉预处理还可以抑制LPS诱导的p65核易位以及IκB-α的磷酸化和降解。我们在体外分析中获得的结果表明,卟啉通过阻断NF-κB的活化来抑制LPS刺激的巨噬细胞中NO的产生。

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