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基于光谱效应关系、成分敲除及超高效液相色谱-质谱联用技术测定九头狮子草中的抗肝癌化合物及其作用机制

Anti-Hepatoma Compound Determination by the Method of Spectrum Effect Relationship, Component Knock-Out, and UPLC-MS in (L.)Frodin Harms and Its Mechanism.

作者信息

Liu Xuqiang, Jiang Nan, Xu Xiaoqing, Liu Cunyu, Liu Zhenhua, Zhang Yan, Kang Wenyi

机构信息

National R & D Center for Edible Fungus Processing Technology, Henan University, Kaifeng, China.

School of Biomedical Sciences, Huaqiao University, Xiamen, China.

出版信息

Front Pharmacol. 2020 Sep 9;11:1342. doi: 10.3389/fphar.2020.01342. eCollection 2020.

Abstract

(L.)Frodin, a kind of Traditional Chinese Medicine, is commonly used in anti-inflammatory, analgesic, anti-viral, anti-tumor, and hemostasis. This study aimed to determine the anti-hepatoma components and its mechanism from the leaves of . The spectrum-effect relationships were analyzed by the method of Partial least squares, indicating that P1, P2, and P10 were positively correlated to inhibitory activity of Huh7 cells. Whereas others were negatively correlated. The technologies of component knock-out and UPLC-MS were used to determine compounds as 3,4-Dicaffeoylquinic acid (P6), 3,5-Dicaffeoylquinic acid (P7), 3-Hydroxy-lup-20(29)-ene-23,28-dioic acid (P10, named Compound A). The results forecasted that Compound A had the best correlation with inhibitory activity. The effects of Compound A on the activities of human hepatoma cells (Huh7, SMMC-7721, HepG 2) and normal hepatocytes (L0-2, Chang liver) were evaluated. Cell apoptosis was observed with inverted microscope and flow cytometer. In addition, the proteins, related to apoptosis, were detected by Western blot. The results showed that Compound A (400 nM) could significantly inhibit the activity of three hepatoma cells ( < 0.001) with slight toxicity to normal hepatocytes, and the IC values were 285.3 and 315.1 nM, respectively, which were consistent with the prediction of spectrum-effect relationships. After treatment with Compound A, the number of hepatoma cells decreased significantly. And the apoptosis rate of Huh7 cells increased significantly ( < 0.001) in Compound A (200, 400 nM) groups, SMMC-7721 and HepG 2 were directly necrotic. Compound A groups could significantly improve the level of intracellular reactive oxygen species (ROS) ( < 0.05, < 0.001) in Huh7 with no effect on normal hepatocytes. The content of apoptotic protein (Bax and Bim) in mitochondria was significantly increased in Compound A groups ( < 0.001). On the contrary, the content of anti-apoptotic protein (Bcl-xL and Mcl-1) decreased significantly ( < 0.001). These results demonstrated that Compound A was the main anti-hepatoma active component in the leaves. It achieved the effect of promoting apoptosis of Huh7 cells by regulating the levels of ROS and Bcl-2 family protein in mitochondrial apoptosis pathway.

摘要

(L.)佛多因是一种中药,常用于抗炎、镇痛、抗病毒、抗肿瘤和止血。本研究旨在从[植物名称]叶中确定抗肝癌成分及其作用机制。采用偏最小二乘法分析谱效关系,结果表明P1、P2和P10与Huh7细胞的抑制活性呈正相关,而其他成分呈负相关。采用成分敲除技术和超高效液相色谱-质谱联用技术确定化合物为3,4-二咖啡酰奎宁酸(P6)、3,5-二咖啡酰奎宁酸(P7)、3-羟基羽扇豆-20(29)-烯-23,28-二酸(P10,命名为化合物A)。结果预测化合物A与抑制活性的相关性最佳。评估了化合物A对人肝癌细胞(Huh7、SMMC-7721、HepG 2)和正常肝细胞(L0-2、Chang liver)活性的影响。用倒置显微镜和流式细胞仪观察细胞凋亡。此外,通过蛋白质免疫印迹法检测与凋亡相关的蛋白质。结果表明,化合物A(400 nM)能显著抑制三种肝癌细胞的活性(P<0.001),对正常肝细胞毒性轻微,其IC值分别为285.3和315.1 nM, 这与谱效关系的预测结果一致。用化合物A处理后,肝癌细胞数量显著减少。在化合物A(200、400 nM)组中,Huh7细胞的凋亡率显著增加(P<0.001),SMMC-7721和HepG 2细胞直接坏死。化合物A组可显著提高Huh7细胞内活性氧(ROS)水平(P<0.05,P<0.001),而对正常肝细胞无影响。化合物A组线粒体中凋亡蛋白(Bax和Bim)的含量显著增加(P<0.001)。相反,抗凋亡蛋白(Bcl-xL和Mcl-1)的含量显著降低(P<0.001)。这些结果表明,化合物A是[植物名称]叶中主要的抗肝癌活性成分。它通过调节线粒体凋亡途径中ROS和Bcl-2家族蛋白的水平,实现了促进Huh7细胞凋亡的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afb9/7509203/648327b381c0/fphar-11-01342-g001.jpg

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