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薁类化合物对小鼠巨噬细胞样细胞中脂多糖刺激的一氧化氮生成的抑制作用。

Inhibition of LPS-stimulated NO production in mouse macrophage-like cells by azulenes.

作者信息

Hashiba Kana, Yokoyama Keiko, Wakabayashi Hidetsugu, Hashimoto Ken, Satoh Kazue, Kurihara Teruo, Motohashi Noboru, Sakagami Hiroshi

机构信息

Faculty of Science, Josai University, Sakado, Saitama, Japan.

出版信息

Anticancer Res. 2004 Nov-Dec;24(6):3939-44.

Abstract

We investigated the effect of twenty-seven azulenes on nitric oxide (NO) production by mouse macrophage-like Raw 264.7 cells. No azulene derivative alone induced NO production by the Raw 264.7 cells, but inhibited lipopolysaccharide (LPS)-stimulated NO production to various extents. The ability of azulenes to inhibit NO generation by activated macrophages was generally increased when their cytotoxic activity declined. Western blot and RT-PCR analyses demonstrated that the most potent compound, 1,3-difluoroazulene [11], slightly inhibited the expression of inducible NO synthase (iNOS), but only at extremely high concentrations. ESR spectroscopy showed that [11] did not produce radical under alkaline condition, nor scavenged O2- (generated by HX-XOD reaction) or NO (generated by NOC-7). These data suggest that the inhibitory effect of [11] may be produced via a mechanism other than iNOS induction and a radical-mediated mechanism.

摘要

我们研究了27种薁类化合物对小鼠巨噬细胞样Raw 264.7细胞产生一氧化氮(NO)的影响。单独的薁类衍生物均未诱导Raw 264.7细胞产生NO,但不同程度地抑制了脂多糖(LPS)刺激的NO产生。当薁类化合物的细胞毒性活性下降时,其抑制活化巨噬细胞产生NO的能力通常会增强。蛋白质免疫印迹和逆转录聚合酶链反应(RT-PCR)分析表明,最有效的化合物1,3-二氟薁[11]仅在极高浓度下轻微抑制诱导型一氧化氮合酶(iNOS)的表达。电子自旋共振光谱显示,[11]在碱性条件下不产生自由基,也不清除超氧阴离子(由黄嘌呤-黄嘌呤氧化酶反应产生)或NO(由NOC-7产生)。这些数据表明,[11]的抑制作用可能通过iNOS诱导以外的机制和自由基介导的机制产生。

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