Extraction and purification of total flavonoids from pine needles of Cedrus deodara contribute to anti-tumor in vitro

杨梅素 赫拉 传统医学 山奈酚 MTT法 类黄酮 槲皮素 IC50型 异鼠李素 人口 化学 细胞凋亡 流式细胞术 体外 药理学 分子生物学 医学 生物 生物化学 抗氧化剂 环境卫生
作者
Xiaofeng Shi,Lingxin Chen,Junmin Zhang,Pengbin Hu,Wei Shen,Bin Fan,Qinghua Ma,Xindi Wang
出处
期刊:BMC Complementary and Alternative Medicine [BioMed Central]
卷期号:16 (1) 被引量:37
标识
DOI:10.1186/s12906-016-1249-z
摘要

Cedrus deodara is one of the traditional Chinese medicinal herbs that exhibits a line of biological activities. The current study extracted the total flavonoids from the pine needles of Cedrus deodara (TFPNCD), and investigated its anti-cancer effects in tumor cell lines. The total flavonoids was extracted from pine needles of Cedrus deodara by ethanol hot refluxing and purified by HPD722 macroporous resin. The contents of total flavonoids and the active ingredients of TFPNCD were analyzed through UV and HPLC. MTT assay was used to investigate its inhibitory effect on tumor cell lines. The flow cytometry was employed to determine the apoptosis and cell cycle distribution after treated TFPNCD on HepG2 cells. The TFPNCD, in which the contents of total flavonoid reached up to 54.28 %, and the major ingredients of myricetin, quercetin, kaempferol and isorhamnetin in TFPNCD were 1.89, 2.01, 2.94 and 1.22 mg/g, respectively. The MTT assays demonstrated that TFPNCD inhibited the growth of HepG2 cells in a dose-dependent manner, with the IC50 values of 114.12 μg/mL. By comparison, TFPNCD inhibited the proliferation to a less extent in human cervical carcinoma HeLa, gastric cancer MKN28 cells, glioma SHG-44 cells and lung carcinoma A549 than HepG2 cells. We found that even at the lower doses, the total flavonoids effectively inhibited the proliferation of HepG2 cells. Comparison of IC50 values implicated that HepG2 cells might be more sensitive to the treatment with total flavonoids. TFPNCD was able to increase the population of HepG2 cells in G0 /G1 phase. Meanwhile, TFPNCD treatment increased the percentage of apoptotic HepG2 cells. These data suggested that TFPNCD might have therapeutic potential in cancer through the regulation of cell cycle and apoptosis.

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