Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan.
In Vivo. 2011 May-Jun;25(3):367-73.
The MeOH extracts from aerial part and roots of Rhinacanthus nasutus were investigated for new biological activities.
The MeOH extract of the root was stepwise separated by organic solvents into n-hexane, EtOAc, n-BuOH and H(2)O layer fractions. Cytotoxic activity against human tumor and normal cells was determined by the MTT method. Nitric oxide (NO) was determined by the Griess method. Osteoclastogenesis was monitored by tartrate-resistant acid phosphatase (TRAP) activity.
The MeOH extract of the root showed much higher tumor-specific cytotoxicity than that of the aerial part. The EtOAc fraction of the root showed the highest tumor-specific cytotoxicity, followed by the n-BuOH, n-hexane and H(2)O fractions. None of the four fractions protected the cells from the cytotoxicity of UV irradiation. The n-BuOH fraction not only stimulated NO production by mouse macrophage-like RAW264.7 cells, but also inhibited the lipopolysaccharide (LPS)-stimulated NO production. The EtOAc fraction inhibited the receptor activator for nuclear factor-κB ligand (RANKL)-stimulated osteoclastogenesis of the RAW264.7 cells most potently, followed by the n-hexane, n-BuOH and H(2)O fractions. The n-BuOH fraction slightly, but significantly stimulated osteoclastogenesis.
Antitumor and macrophage/osteoclast-modulating substances are enriched in EtOAc and n-BuOH fractions of MeOH extract of R. nasutus roots.
对独角金(Rhinacanthus nasutus)地上部分和根的甲醇提取物进行了新的生物活性研究。
采用有机溶剂分步法,将根的甲醇提取物分离为正己烷、乙酸乙酯、正丁醇和水层。用 MTT 法测定对人肿瘤细胞和正常细胞的细胞毒性。用 Griess 法测定一氧化氮(NO)。用抗酒石酸酸性磷酸酶(TRAP)活性监测破骨细胞生成。
根的甲醇提取物对肿瘤细胞的特异性细胞毒性明显高于地上部分。根的乙酸乙酯部分显示出最高的肿瘤特异性细胞毒性,其次是正丁醇、正己烷和水部分。这四个部分都不能保护细胞免受紫外线照射的细胞毒性。正丁醇部分不仅刺激小鼠巨噬细胞样 RAW264.7 细胞产生一氧化氮(NO),还抑制脂多糖(LPS)刺激的 NO 产生。乙酸乙酯部分最有效地抑制核因子-κB 配体(RANKL)刺激的 RAW264.7 细胞破骨细胞生成,其次是正己烷、正丁醇和水部分。正丁醇部分略有但显著地刺激破骨细胞生成。
独角金根的甲醇提取物的乙酸乙酯和正丁醇部分富含抗肿瘤和巨噬细胞/破骨细胞调节物质。