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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Antiliver Fibrosis Screening of Active Ingredients from Apium graveolens L. Seeds via GC-TOF-MS and UHPLC-MS/MS
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Antiliver Fibrosis Screening of Active Ingredients from Apium graveolens L. Seeds via GC-TOF-MS and UHPLC-MS/MS

机译:通过GC-TOF-MS和UHPLC-MS / MS从Apium Graveolens L.种子中取出活性成分的纤维化筛选

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Although several studies have been performed on Apium graveolens L.(celery) seeds, their antiliver fibrosis effects remain to be unexplored. Firstly, we detected the effects of celery seeds extracted with different concentrations of aqueous ethanol on the proliferation of HSC-LX2 cells. Then, we detected the effects of fractions of the optimal effect extract on the proliferation and apoptosis of HSC-LX2 cells. Finally, the compounds of petroleum ether (PP), ethyl acetate (PE), n-butyl alcohol (PB), and water fractions (PW) of the optimal effect extract were determined by GC-TOF-MS and UHPLC-MS/MS, to confirm the potentially antifibrotic compounds combined with pharmacodynamic experiment of monomer compounds in vitro. The results revealed that 60% ethanol extract of celery seeds (60-extract) exhibited remarkable inhibition effect on the proliferation of HSC-LX2 cells compared with 95% ethanol and aqueous extract. Besides, it validated that the inhibition rates of PP, PE, PB, and PW on the proliferation of HSC-LX2 cells were 75.14%, 73.52%, 54.09%, and 43.36%, and their percentage of apoptotic cells were 37.5%, 4.3%, 0.7%, and 0.1% at high doses, respectively. Additionally, it was manifested that apigenin, aesculetin, and butylphthalide have major contribution to the overall compounds of celery seeds, and the inhibition effects on the cell proliferation clearly elevated with increase in their contents. In essence, apigenin, aesculetin, and butylphthalide may hopefully become the natural products of antiliver fibrosis, which laid a foundation for the subsequent development of celery seeds as antiliver fibrosis drugs.
机译:虽然已经在Apium Graveolens L.(芹菜)种子上进行了几项研究,但它们的解除纤维化效应仍然是未开发的。首先,我们检测到用不同浓度的乙醇萃取芹菜种子对HSC-LX2细胞的增殖的影响。然后,我们检测到最佳效果提取物的效果对HSC-LX2细胞的增殖和凋亡的影响。最后,通过GC-TOF-MS和UHPLC-MS / MS测定最佳效果提取物的石油醚(PP),乙酸乙酯(PE),正丁醇(PB)和水分分数(PW)的化合物,确认潜在的抗纤维化化合物在体外与单体化合物的药物动力学实验相结合。结果表明,与95%乙醇和含水提取物相比,芹菜种子(60-提取物)的60%乙醇提取物对HSC-LX2细胞的增殖表现出显着的抑制作用。此外,它验证了PP,PE,Pb和PW对HSC-LX2细胞增殖的抑制率为75.14%,73.52%,54.09%和43.36%,其凋亡细胞的百分比为37.5%,4.3高剂量分别为%,0.7%和0.1%。此外,它表现出嗜肝素,嗜脲素和丁基苯二甲苯二甲酸丁酯对芹菜种子的整体化合物具有主要贡献,以及对细胞增殖的抑制作用随着其内容物的增加而明显升高。从本质上讲,Apigenin,Aesculetin和丁基苯二甲苯二甲酸丁醇可以成为纤维化的天然产物,其为随后的芹菜种子作为纤维化药物奠定了基础。

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