首页> 美国卫生研究院文献>Biochemical Journal >Cyclolinteinone a sesterterpene from sponge Cacospongia linteiformis prevents inducible nitric oxide synthase and inducible cyclo-oxygenase protein expression by blocking nuclear factor-kappaB activation in J774 macrophages.
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Cyclolinteinone a sesterterpene from sponge Cacospongia linteiformis prevents inducible nitric oxide synthase and inducible cyclo-oxygenase protein expression by blocking nuclear factor-kappaB activation in J774 macrophages.

机译:Cyclolinteinone是来自海绵状Cacospongia linteiformis的一种酯基萜烯可通过阻断J774巨噬细胞中的核因子-κB活化来阻止诱导型一氧化氮合酶和诱导型环加氧酶蛋白的表达。

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摘要

We investigated the effect of cyclolinteinone, a sesterterpene from Caribbean sponge Cacospongia linteiformis, on inducible NO synthase (iNOS) and cyclo-oxygenase-2 (COX-2) protein expression in lipopolysaccharide (LPS)-stimulated J774 macrophages. Incubation of J774 cells with LPS (1 microgram/ml) caused an increase of both iNOS and COX-2 protein expression, which was prevented in a concentration-dependent fashion by cyclolinteinone (12.5, 25 and 50 microM). Electrophoretic mobility-shift assay indicated that cyclolinteinone blocked the activation of nuclear factor-kappaB (NF-kappaB), a transcription factor necessary for either iNOS or COX-2 induction. Cyclolinteinone also blocked disappearance of I(kappa)B-alpha from cytosolic fraction and nuclear translocation of NF-kappaB subunits p50 and p65. These results show that cyclolinteinone down-regulates iNOS and COX-2 protein expression by inhibiting NF-kappaB activation and suggest that it may represent a novel anti-inflammatory compound capable of controlling the excessive production of prostaglandins and nitric oxide occurring in several inflammatory diseases.
机译:我们调查了环亚麻酮,一种来自加勒比海海绵小球藻的酯基萜烯,对脂多糖(LPS)刺激的J774巨噬细胞中诱导型NO合酶(iNOS)和环加氧酶-2(COX-2)蛋白表达的影响。用LPS(1微克/毫升)孵育J774细胞会引起iNOS和COX-2蛋白表达的增加,而环戊烯酮(12.5、25和50 microM)以浓度依赖性的方式阻止了这种表达。电泳迁移率迁移分析表明,环亚麻酮抑制了iNOS或COX-2诱导所必需的转录因子核因子-κB(NF-κB)的活化。 Cyclolinteinone还可以阻止I(kappa)B-α从胞浆中消失,并阻止NF-kappaB亚基p50和p65的核转运。这些结果表明,环亚麻酮可以通过抑制NF-κB的活化来下调iNOS和COX-2蛋白的表达,并表明它可能代表一种新型的抗炎化合物,能够控制前列腺素和一氧化氮的过量产生,而前列腺素和一氧化氮在几种炎症性疾病中均会发生。

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