Hegazy Mohamed-Elamir F, Matsuda Hisashi, Nakamura Seikou, Yabe Mikuko, Matsumoto Tomoko, Yoshikawa Masayuki
Kyoto Pharmaceutical University, Kyoto, Japan.
Chem Pharm Bull (Tokyo). 2012;60(3):363-70. doi: 10.1248/cpb.60.363.
The methylene chloride-methanol (1 : 1) extract from the air-dried aerial parts of wild Pulicaria undulata collected in North Sinia, Egypt, showed inhibitory effects on lipopolysaccharide (LPS)-induced production of nitric oxide (NO) in RAW264.7 macrophages. From the extract, three new sesquiterpenes named 5α-hydroperoxyivalin, 8-epi-xanthanol, and 8-epi-isoxanthanol were isolated together with four known sesquiterpenes. The structure of each new sesquiterpenes was determined on the basis of physicochemical and chemical evidence. In addition, all the sesquiterpenoids significantly inhibited the production of NO. Ivalin (IC50=2.0 μM) and 2α-hydroxyalantolactone (1.8 μM) showed particularly strong inhibitory effects, but had strong cytotoxic effects as well. Furthermore, ivalin and 2α-hydroxyalantolactone concentration-dependently reduced inducible NO synthase (iNOS) protein levels in RAW264.7 cells.
从埃及北西奈采集的野生波叶旋覆花干燥地上部分中提取的二氯甲烷 - 甲醇(1∶1)提取物,对脂多糖(LPS)诱导的RAW264.7巨噬细胞中一氧化氮(NO)的产生具有抑制作用。从该提取物中分离出了三种新的倍半萜,分别命名为5α - 氢过氧化艾瓦林、8 - 表 - 黄原醇和8 - 表 - 异黄原醇,以及四种已知的倍半萜。根据物理化学和化学证据确定了每种新倍半萜类化合物的结构。此外,所有倍半萜类化合物均显著抑制NO的产生。艾瓦林(IC50 = 2.0 μM)和2α - 羟基阿兰内酯(1.8 μM)表现出特别强的抑制作用,但也具有较强的细胞毒性作用。此外,艾瓦林和2α - 羟基阿兰内酯在RAW264.7细胞中浓度依赖性地降低诱导型一氧化氮合酶(iNOS)蛋白水平。