首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >The effect of lipid peroxidation products on reactive oxygen species formation and nitric oxide production in lipopolysaccharide-stimulated RAW 264.7 macrophages.
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The effect of lipid peroxidation products on reactive oxygen species formation and nitric oxide production in lipopolysaccharide-stimulated RAW 264.7 macrophages.

机译:脂质过氧化产物对脂多糖刺激的RAW 264.7巨噬细胞中活性氧形成和一氧化氮生成的影响。

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摘要

Lipid peroxidation induced by oxidants leads to the formation of highly reactive metabolites. These can affect various immune functions, including reactive oxygen species (ROS) and nitric oxide (NO) production. The aim of the present study was to investigate the effects of lipid peroxidation products (LPPs) - acrolein, 4-hydroxynonenal, and malondialdehyde - on ROS and NO production in RAW 264.7 macrophages and to compare these effects with the cytotoxic properties of LPPs. Macrophages were stimulated with lipopolysaccharide (0.1 mug/ml) and treated with selected LPPs (concentration range: 0.1-100 muM). ATP test, luminol-enhanced chemiluminescence, Griess reaction, Western blotting analysis, amperometric and total peroxyl radical-trapping antioxidant parameter assay were used for determining the LPPs cytotoxicity, ROS and NO production, inducible nitric oxide synthase expression, NO scavenging, and antioxidant properties of LPPs, respectively. Our study shows that the cytotoxic action of acrolein and 4-hydroxynonenal works in a dose- and time-dependent manner. Further, our results imply that acrolein, 4-hydroxynonenal, and malondialdehyde can inhibit, to a different degree, ROS and NO production in stimulated macrophages, partially independently of their toxic effect. Also, changes in enzymatic pathways (especially NADPH-oxidase and nitric oxide synthase inhibition) and NO scavenging properties are included in the downregulation of reactive species formation.
机译:氧化剂引起的脂质过氧化作用导致高反应性代谢物的形成。这些会影响各种免疫功能,包括活性氧(ROS)和一氧化氮(NO)的产生。本研究的目的是研究脂质过氧化产物(LPP)-丙烯醛,4-羟基壬烯醛和丙二醛-对RAW 264.7巨噬细胞中ROS和NO的产生,并将这些影响与LPP的细胞毒性进行比较。用脂多糖(0.1杯/毫升)刺激巨噬细胞,并用选定的LPPs(浓度范围:0.1-100μM)处理。使用ATP测试,鲁米诺增强化学发光,Griess反应,Western印迹分析,安培和总过氧自由基捕获抗氧化剂参数测定来确定LPP的细胞毒性,ROS和NO产生,诱导型一氧化氮合酶表达,NO清除和抗氧化剂特性LPPs。我们的研究表明,丙烯醛和4-羟基壬烯醛的细胞毒性作用呈剂量和时间依赖性。此外,我们的结果表明,丙烯醛,4-羟基壬烯醛和丙二醛可以在不同程度上抑制受刺激的巨噬细胞中ROS和NO的产生,部分独立于它们的毒性作用。同样,酶途径的改变(特别是NADPH-氧化酶和一氧化氮合酶抑制)和NO清除特性也包括在反应物种形成的下调中。

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