College of Life Sciences, Northwest Normal University, Lanzhou 730070, People's Republic of China.
Nat Prod Res. 2011 Apr;25(7):669-83. doi: 10.1080/14786410802497398. Epub 2010 Feb 23.
Four xanthones were isolated from Gentianopsis paludosa Ma and were identified by modern spectroscopic methods. Cytotoxicity of the four xanthones was tested on HepG2 cells and HL-60 cells by sulphorhodamine B (SRB) assay. Clonogenic survival assay, trypan blue exclusion method, AO/EB staining and DNA fragmentation assay were conducted to investigate the effect on growth inhibition and apoptosis in the two cell lines in vitro. At the same time, structure-activity relationships (SARs) of the xanthones were investigated. The results showed that the xanthones had significant cytotoxicity and inhibition of proliferation in both HepG2 cells and HL-60 cells, and could induce apoptosis in these two cell lines. SARs indicated that the methoxy group had more cytotoxic contribution than the hydroxyl group at site C-8 in the structural scaffold of xanthone. The glycosidea at site C-1 may aggravate the stereospecific blockade of compound 4 and reduced its cytotoxic activity.
从獐牙菜中分离得到 4 个酮,并通过现代光谱方法鉴定。采用磺基罗丹明 B(SRB)法检测了这 4 种酮对 HepG2 细胞和 HL-60 细胞的细胞毒性。通过克隆存活试验、台盼蓝排斥法、AO/EB 染色和 DNA 片段化试验,研究了它们对这两种细胞系体外生长抑制和凋亡的影响。同时,还研究了酮的构效关系(SARs)。结果表明,酮类化合物对 HepG2 细胞和 HL-60 细胞均具有显著的细胞毒性和增殖抑制作用,并能诱导这两种细胞系发生凋亡。SARs 表明,在酮类化合物的结构骨架中,C-8 位的甲氧基比羟基具有更强的细胞毒性贡献。C-1 位的糖苷基可能会加剧化合物 4 的立体特异性阻滞,降低其细胞毒性活性。