Graduate School of Science and Technology, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, Japan.
J Biochem. 2012 Jan;151(1):65-74. doi: 10.1093/jb/mvr115. Epub 2011 Oct 5.
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.
琼胶,从一种可食用的红藻(紫菜)中提取,是一种具有多种生物活性的硫酸多糖,包括抗肿瘤、抗氧化和免疫调节活性。在本研究中,我们研究了琼胶对小鼠巨噬细胞 RAW264.7 细胞中一氧化氮(NO)产生的影响。尽管在测试浓度范围内(10-500μg/ml),琼胶对 RAW264.7 细胞中 NO 或肿瘤坏死因子-α(TNF-α)产生没有明显的活性,但我们首次发现琼胶抑制脂多糖(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 500μg/ml 琼胶存在的情况下,完全抑制 LPS 处理的 RAW264.7 细胞中 NO 的产生和 iNOS 的表达。另一方面,琼胶对 LPS 刺激的 RAW264.7 细胞中 TNF-α的分泌仅有轻微的影响。使用带有核因子-κB(NF-κB)共有序列的红外染料标记寡核苷酸的电泳迁移率变动分析(EMSA)表明,琼胶抑制了 LPS 诱导的 NF-κB 激活。琼胶预处理还抑制了 LPS 诱导的 p65 的核易位,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,琼胶通过阻断 NF-κB 激活来抑制 LPS 刺激的巨噬细胞中 NO 的产生。