天然产物研究与开发 ›› 2017, Vol. 29 ›› Issue (7): 1193-1198.doi: 10.16333/j.1001-6880.2017.7.020

• 开发研究 • 上一篇    下一篇

香叶木素和香叶木素-7-O-β-D-吡喃葡萄糖苷的生物活性比较

王月华1,杨红英1,付崇罗1,李爱峰2,玄红专1*   

  1. 1 聊城大学生命科学学院;2 聊城大学化学与化工学院,聊城 252059
  • 出版日期:2017-07-29 发布日期:2017-08-11

Comparison of Biological Activities of Diosmetin and Diosmetin-7-O-β-D-Glucopyranoside

WANG Yue-hua1,YANG Hong-ying1,FU Chong-luo1,LI Ai-feng2,XUAN Hong-zhuan1*   

  1. 1 School of Life Science,Liaocheng University; 2 School of Chemical & Chemical engineering,Liaocheng 252059,China
  • Online:2017-07-29 Published:2017-08-11

摘要: 研究香叶木素和香叶木素-7-O-β-D-吡喃葡萄糖苷对不同肿瘤细胞(MCF-7、MDA-MB-231和A549)和血管内皮细胞(HUVECs)的细胞毒性及作用机制。正常培养的肺腺癌细胞(A549)、乳腺癌细胞(MCF-7、 MDA-MB-231)及血管内皮细胞(HUVECs)经不同浓度的香叶木素和香叶木素-7-O-β-D-吡喃葡萄糖苷(20、 40、80、160 μM)分别处理24和48 h,倒置显微镜观察细胞形态,SRB法检测细胞存活率;吖啶橙染色观察细胞核凝集和片段化;Hoechst 33258检测细胞凋亡;荧光探针DCHF检测细胞内活性氧(ROS);Western blot检测膜联蛋白A7(ANXA7)、P62、procaspase3和LC3的表达。结果表明,香叶木素以剂量依赖的方式抑制肿瘤细胞MDA-MB-231、MCF-7、A549的增殖和去血清条件下血管内皮细胞的增殖,通过上调LC3-Ⅱ的水平,促进肿瘤细胞自噬。香叶木素-7-O-β-D-吡喃葡萄糖苷对去血清条件下血管内皮细胞有保护作用,显著降低去血清条件下血管内皮细胞的细胞凋亡和细胞核片段凝集,显著降低细胞内ROS水平,下调caspase3和LC3-Ⅱ的水平。香叶木素和香叶木素-7-O-β-D-吡喃葡萄糖苷具有不同的生物活性。香叶木素是一种潜在的抗肿瘤化合物,而香叶木素-7-O-β-D-吡喃葡萄糖苷可能成为一种保护HUVECs的有效药物。

关键词: 香叶木素, 香叶木素-7-O-&beta, -D-吡喃葡萄糖苷, 细胞凋亡, 自噬, 活性氧

Abstract: To compare the biological activities of diosmetin and diosmetin-7-O-β-D-glucopyranoside extracted from the peel of Trichosanthes kirilowii Maxim,we investigated their cytotoxicity on different cancer cells (MCF-7,MDA-MB-231 and A549) and human umbilical vein endothelial cells (HUVECs),and the probable mechanisms were also preliminary studied.Cell viability,morphological changes of nuclei and the expression of procaspase 3,LC3B,p62 and annexin A7 (ANXA7) were measured by sulforhodamine B (SRB) assay,acridine orange and Hoechst33258 staining and western blot respectively.Intracellular reactive oxygen species (ROS) level was determined by utilizing a fluorescent probe,2′,7′-dichlorodihydrofluorescin (DCHF).SRB assay showed that diosmetin had significant inhibition effects on the proliferation of MCF-7,MDA-MB-231 and A549 human cancer cell lines in a dose-and time- dependent manner,and induced HUVECs deprived of serum apoptosis.Western blot results showed that diosmetin induced tumor cell autophagy by increasing LC3-II level.However,diosmetin-7-O-β-D-glucopyranoside had a protective effect on HUVECs deprived of serum.Hoechst 33258 staining and acridine orange staining results showed apoptosis and nuclei fragments in HUVECs deprived of serum significantly decreased after treated with diosmetin-7-O-β-D-glucopyranoside respectively.Moreover,diosmetin-7-O-β-D-glucopyranoside significantly decreased ROS levels and inhibited caspase 3 and LC3-II level in HUVECs deprived of serum.Diosmetin and diosmetin-7-O-β-D-glucopyranoside had different biological activities.Diosmetin was a good antitumor agent whereas diosmetin-7-O-β-D-glucopyranoside might be a promising substituent to protect HUVECs.

Key words: diosmetin, diosmetin-7-O-&beta, -D-glucopyranoside, apoptosis, autophagy, reactive oxygen species