Hashiba Kana, Yokoyama Keiko, Wakabayashi Hidetsugu, Hashimoto Ken, Satoh Kazue, Kurihara Teruo, Motohashi Noboru, Sakagami Hiroshi
Faculty of Science, Josai University, Sakado, Saitama, Japan.
Anticancer Res. 2004 Nov-Dec;24(6):3939-44.
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.
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。