Anh La Hoang, Quan Nguyen Van, Lam Vu Quang, Iuchi Yu, Takami Akiyoshi, Teschke Rolf, Xuan Tran Dang
Transdisciplinary Science and Engineering Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Hiroshima 739-8529, Japan.
Division of Hematology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute 480-1195, Japan.
Plants (Basel). 2020 Dec 31;10(1):69. doi: 10.3390/plants10010069.
is an invasive weed that seriously threatens agricultural production and economics worldwide. In this research, dried aerial parts of were extracted, applying Soxhlet and liquid-liquid phase methods to acquire the total crude (T-Anvi), hexane (H-Anvi), ethyl acetate (E-Anvi), butanol (B-Anvi), and water (W-Anvi) extracts, respectively. In which, T-Anvi contains the highest total phenolic and flavonoid contents (24.80 mg gallic acid and 37.40 mg rutin equivalents per g dry weight, respectively). Via anti-radical (ABTS and DPPH), and reducing power assays, E-Anvi exhibits the most potent activities (IC = 13.96, 43.59 and 124.11 µg/mL, respectively), stronger than butylated hydroxytoluene (BHT), a standard antioxidant, while the lipid peroxidation inhibitory effect of E-Anvi (LPI = 90.85% at the concentration of 500 µg/mL) is close to BHT. E-Anvi shows the most substantial inhibition (IC = 2.58 mg/mL) on tyrosinase. Notably, α-amylase is significantly suppressed by H-Anvi (IC = 0.72 mg/mL), over twice stronger than the positive control, palmitic acid. In the cytotoxic assay, E-Anvi is the strongest extract inhibiting K562 cells (IC = 112.01 µg/mL). Meanwhile, T-Anvi shows the highest prevention on Meg-01 expansion (IC = 91.40 µg/mL). Dominant compounds detected in E-Anvi by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (HPLC-ESI-MS/MS) are identified as flavonoids. However, among four major compounds identified in H-Anvi by gas chromatography-mass spectrometry (GC-MS), palmitic acid and phytol are the most abundant compounds with peak areas of 27.97% and 16.42%, respectively. In essence, this is the first report describing that is a potential natural source of antioxidants, tyrosinase and α-amylase inhibitors, and anti-chronic myeloid leukemia (CML) agents which may be useful in future therapeutics as promising alternative medicines.
是一种入侵性杂草,严重威胁着全球的农业生产和经济。在本研究中,对[植物名称未给出]的干燥地上部分进行提取,分别采用索氏提取法和液 - 液萃取法获得总粗提物(T - Anvi)、己烷提取物(H - Anvi)、乙酸乙酯提取物(E - Anvi)、丁醇提取物(B - Anvi)和水提取物(W - Anvi)。其中,T - Anvi的总酚和黄酮含量最高(每克干重分别为24.80毫克没食子酸和37.40毫克芦丁当量)。通过抗自由基(ABTS和DPPH)及还原能力测定,E - Anvi表现出最强的活性(IC值分别为13.96、43.59和124.11微克/毫升),比标准抗氧化剂丁基羟基甲苯(BHT)更强,而E - Anvi的脂质过氧化抑制作用(在500微克/毫升浓度下LPI = 90.85%)与BHT相近。E - Anvi对酪氨酸酶的抑制作用最强(IC = 2.58毫克/毫升)。值得注意的是,H - Anvi对α - 淀粉酶有显著抑制作用(IC = 0.72毫克/毫升),比阳性对照棕榈酸强两倍多。在细胞毒性试验中,E - Anvi是抑制K562细胞最强的提取物(IC = 112.01微克/毫升)。同时,T - Anvi对Meg - 01细胞增殖的预防作用最强(IC = 91.40微克/毫升)。通过高效液相色谱 - 电喷雾电离 - 串联质谱(HPLC - ESI - MS/MS)在E - Anvi中检测到的主要化合物被鉴定为黄酮类化合物。然而,通过气相色谱 - 质谱(GC - MS)在H - Anvi中鉴定出的四种主要化合物中,棕榈酸和叶绿醇是含量最丰富的化合物,峰面积分别为27.97%和16.42%。本质上,这是首次报道[植物名称未给出]是抗氧化剂、酪氨酸酶和α - 淀粉酶抑制剂以及抗慢性粒细胞白血病(CML)药物的潜在天然来源,这些可能在未来治疗中作为有前景的替代药物发挥作用。