Tashiro Miyuki, Suzuki Fumika, Shirataki Yoshiaki, Yokote Yoshiko, Akahane Kiso, Motohashi Noboru, Ishihara Mariko, Jiang Yi, Sakagami Hiroshi
Department of Dental Pharmacology, Meikai University School of Dentistry, Sakado, Saitama, Japan.
Anticancer Res. 2002 Jan-Feb;22(1A):53-8.
We investigated the effect of 2 flavanones and 8 chemically-defined prenylflavanones on the growth and activation of mouse macrophage-like Raw 264.7 cells. Amino acid analysis in the culture medium demonstrated the rapid consumption of serine and glutamine by Raw264.7 cells, suggesting the necessity to supplement these amino acids for the prolonged culture. Naringenin and hesperetin showed little or no cytotoxic activity. However, addition of the isoprenyl group (sophoraflavanone B, euchrestaflavanone A) or the lavandulyl and hydroxyl group (sophoraflavanone G) significantly enhanced the cytotoxic activity. The cytotoxic activity of these compounds was significantly influenced by both log P value and ionization potential. These compounds slightly, but significantly, reduced both nitric oxide (NO) and tumor necrosis factor (TNF) production by lipopolysaccharide (LPS)-stimulated Raw 264.7 cells, regardless of their cytotoxic activity. These data suggest that the macrophage inhibitory effect of prenylflavanones might not be related to their cytotoxic activity.
我们研究了2种黄烷酮和8种化学结构明确的异戊烯基黄烷酮对小鼠巨噬细胞样Raw 264.7细胞生长和活化的影响。培养基中的氨基酸分析表明,Raw264.7细胞能快速消耗丝氨酸和谷氨酰胺,这表明为延长培养时间有必要补充这些氨基酸。柚皮素和橙皮素显示出很少或没有细胞毒性活性。然而,添加异戊烯基(槐黄酮B、宽叶羽扇豆黄酮A)或薰衣草基和羟基(槐黄酮G)显著增强了细胞毒性活性。这些化合物的细胞毒性活性受到log P值和电离势的显著影响。无论其细胞毒性活性如何,这些化合物均能轻微但显著地降低脂多糖(LPS)刺激的Raw 264.7细胞产生的一氧化氮(NO)和肿瘤坏死因子(TNF)。这些数据表明,异戊烯基黄烷酮的巨噬细胞抑制作用可能与其细胞毒性活性无关。