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Docosahexaenoic acid-derived oxidized lipid metabolites modulate the inflammatory response of lipolysaccharide-stimulated macrophages

机译:Docosahexoeno酸衍生的氧化脂质代谢物调节脂质糖刺激的巨噬细胞的炎症反应

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Docosahexaenoic acid (DHA) supplementation has demonstrated beneficial effects in a number of inflammatory diseases. Increasingly, important contributions to its favorable effects are attributed downstream metabolites called docosanoids. Herein, we investigated the role of DHA-derived oxidized lipid metabolites on inflammatory mediator expression by RAW 264.7 murine macrophages. Specifically, macrophage incorporation of DHA, and the resultant biosynthesis of selected pro-resolving docosanoids was quantified. Docosanoid effects on the expression of selected pro-inflammatory cytokines in LPS-stimulated cultures was determined. Macrophages incorporated DHA in significant amounts. In the presence of DHA macrophages produced statistically significant amounts of several putative pro-resolving docosanoids compared to untreated controls. Among them, resolvins D1 and D2 and maresin 1 abrogated COX-2 and IL-1 beta gene expression in LPS-stimulated macrophages. In addition to these mediators, protectin DX inhibited LPS-stimulated macrophage expression of IL-6. Our results demonstrate that macrophages incorporate DHA in quantities sufficient for the biosynthesis of biologically relevant concentrations of a number of pro-resolving docosanoids, certain of which modulate the inflammatory response of macrophages under conditions mimicking acute inflammation. These data provide further information on the mechanism(s) by which DHA exerts salutary effects on the inflammatory response of macro-phages.
机译:十二碳己烯酸(DHA)补充在许多炎症疾病中表现出有益的影响。越来越多地对其有利影响的重要贡献是归因于叫做二糖的下游代谢产物。在此,我们研究了DHA-衍生的氧化脂质代谢物对原料264.7鼠巨噬细胞对炎症介质表达的作用。具体而言,定量了DHA的巨噬细胞掺入,以及所选择的促择分离的二糖苷的所得生物合成。测定了对LPS刺激培养物中所选促炎细胞因子的表达的二糖烷。巨噬细胞以大量成分掺入DHA。在DHA巨噬细胞的存在下,与未处理的对照相比,产生统计上显着的多种调节多糖烷烃。其中,在LPS刺激的巨噬细胞中,溶质D1和D2和Maresin 1废除COX-2和IL-1β基因表达。除了这些介质外,Protectin DX抑制IL-6的LPS刺激的巨噬细胞表达。我们的结果表明,巨噬细胞以足以用于生物学相关浓度的生物合成的量的量,其中某些部分在模拟急性炎症的条件下调节巨噬细胞的炎症反应。这些数据提供了关于DHA对宏观噬菌体炎症反应的良效应作用的机制的进一步信息。

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