Sharma Neelesh, Samarakoon Kalpa W, Gyawali Rajendra, Park Yang-Ho, Lee Sung-Jin, Oh Sung Jong, Lee Tae-Hoon, Jeong Dong Kee
Department of Animal Biotechnology, Faculty of Biotechnology, Jeju National University, Jeju 690-756, Korea.
Department of Marine Life Science, Jeju National University, Jeju 690-756, Korea.
Molecules. 2014 Sep 15;19(9):14567-81. doi: 10.3390/molecules190914567.
This study evaluated the chemical composition, antioxidant, anti-inflammatory and anticancer activities of a Euphorbia hirta L. extract. The antioxidant activities of whole E. hirta ethanol extract were determined by electron spin resonance spectrophotometric analysis of 1,1-diphenyl-2-picryl-hydrazyl (DPPH), hydroxyl, and alkyl radical levels and by using an online high-performance liquid chromatography (HPLC)-2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) assay. The E. hirta ethanol extract (0.5 mg/mL) exhibited DPPH-scavenging activity of 61.19% ± 0.22%, while the positive control (0.5 mg/mL ascorbic acid) had 100% ± 0.22% activity. The concentration of the extract required to trap 50% of DPPH (IC50) was 0.205 mg/mL. Online HPLC analysis of the extract also showed strong antioxidant activity. The anti-inflammatory activity of the E. hirta extract was assessed in lipopolysaccharide-induced RAW 264.7 macrophages. The anti-inflammatory activity was highest in the presence of 200 µg/mL E. hirta extract, and nitric oxide production was decreased significantly (p < 0.05). The extract also showed selective anticancer activity at a concentration of 100 µg/mL (p < 0.05). These results indicated that E. hirta may warrant further investigation for the development of antioxidant, anti-inflammatory, and anticancer herbal medications.
本研究评估了大戟草提取物的化学成分、抗氧化、抗炎和抗癌活性。通过对1,1 - 二苯基 - 2 - 苦基肼(DPPH)、羟基和烷基自由基水平进行电子自旋共振分光光度分析以及使用在线高效液相色谱(HPLC)- 2,2'- 联氮 - 双 -(3 - 乙基苯并噻唑啉 - 6 - 磺酸)法来测定大戟草全乙醇提取物的抗氧化活性。大戟草乙醇提取物(0.5 mg/mL)的DPPH清除活性为61.19% ± 0.22%,而阳性对照(0.5 mg/mL抗坏血酸)的活性为100% ± 0.22%。捕获50% DPPH所需的提取物浓度(IC50)为0.205 mg/mL。提取物的在线HPLC分析也显示出较强的抗氧化活性。在脂多糖诱导的RAW 264.7巨噬细胞中评估了大戟草提取物的抗炎活性。在200 µg/mL大戟草提取物存在的情况下,抗炎活性最高,一氧化氮生成量显著降低(p < 0.05)。该提取物在浓度为100 µg/mL时也显示出选择性抗癌活性(p < 0.05)。这些结果表明,大戟草可能值得进一步研究,以开发抗氧化、抗炎和抗癌草药药物。