Yokoyama Keiko, Hashiba Kana, 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):3917-22.
We investigated the effect of 27 tropolones on nitric oxide (NO) production by mouse macrophage-like Raw 264.7 cells. All of these compounds failed to stimulate the Raw 264. 7 cells to produce detectable amounts of NO, but inhibited NO production by lipopolysaccharide (LPS)-activated Raw 264.7 cells to various extents. Generally, the ability of tropolones to inhibit LPS-stimulated NO production was inversely related to their cytotoxic activity. Western blot and RT-PCR analyses demonstrated that the most active compound, 2,4-dibromo-7-methoxytropone [21], significantly reduced both the intracellular concentration of iNOS protein and the expression of iNOS mRNA. ESR spectroscopy showed that [21] did not produce radicals under alkaline condition, nor scavenged NO, produced by NOC-7. These data suggested that the inhibitory effect of [21] on NO production might be generated via the inhibition of iNOS expression, rather than a radical-mediated mechanism.
我们研究了27种托酚酮对小鼠巨噬细胞样Raw 264.7细胞产生一氧化氮(NO)的影响。所有这些化合物均未能刺激Raw 264.7细胞产生可检测量的NO,但不同程度地抑制了脂多糖(LPS)激活的Raw 264.7细胞产生NO。一般来说,托酚酮抑制LPS刺激的NO产生的能力与其细胞毒性活性呈负相关。蛋白质免疫印迹和逆转录聚合酶链反应分析表明,活性最强的化合物2,4-二溴-7-甲氧基托酚酮[21]显著降低了诱导型一氧化氮合酶(iNOS)蛋白的细胞内浓度和iNOS信使核糖核酸(mRNA)的表达。电子自旋共振光谱显示,[21]在碱性条件下不产生自由基,也不清除由NOC-7产生的NO。这些数据表明,[21]对NO产生的抑制作用可能是通过抑制iNOS表达产生的,而不是通过自由基介导的机制。