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机构地区:[1]大连大学生命科学与技术学院,辽宁大连116622
出 处:《华西药学杂志》2014年第4期371-373,共3页West China Journal of Pharmaceutical Sciences
基 金:国家自然科学基金资助项目(批准号:30801509)
摘 要:目的研究油茶皂素7、8对人胃癌SGC-7901细胞的增殖抑制作用及凋亡观察。方法常规培养SGC-7901细胞,采用噻唑蓝(MTT)法检测细胞的活性,而后选用Hoechst33342染色观察细胞的凋亡形态,最后选用AnnexinV/PI双标记法检测细胞的凋亡。结果 5~100μg·mL-1油茶皂素7、20~200μg·mL-1油茶皂素8对人胃癌SGC-7901细胞的抑制作用表现出明显的剂量依赖关系;50μg·mL-1油茶皂素7、100μg·mL-1油茶皂素8处理过的细胞被染色后,部分细胞核内呈现浓染致密的颗粒块状荧光或荧光碎片,表明SGC-7901细胞发生了凋亡;50μg·mL-1油茶皂素7可显著诱导SGC-7901的早期凋亡,早期凋亡率为4.33%,总凋亡率(8.1%)明显大于空白对照组(4.89%),150μg·mL-1油茶皂素8可明显诱导SGC-7901细胞的早期凋亡(2.46%)和晚期凋亡(5.69%)。结论油茶皂素7、8可剂量依赖性抑制SGC-7901细胞的增殖活性,并能诱导SGC-7901细胞凋亡。OBJECTIVE To study the sasanqua saponin 7,8 inhibited the proliferation and apoptosis on human gastric cancer SGC - 7901. METHODS The effect of strian proliferative on SGC -7901 of sasanqua saponin 7,8 by MTT was observe,and Hoechst 33342 staining was chosen and apoptotic debris was found with flow cytometry in SGC -7901. RESULTS Sasanqua saponin 7(5 - 100 μg·mL^- 1 ) and sasanqua saponin 8 ( 20 - 200 μg· mL ^- 1) could significantly inhibit the proliferation in a dose - dependent manner. The part of the nucleus redered stain dense particles block flnrescence or flureseence debris by sasanqua saponin 7 (50 μg·mL^- 1 )and sasanqua saponin 8 ( 100 μg. mL- 1 ). 50 μg· mL^- 1 sasanqua saponin 7 could significantly induced early apoptosis of SGC - 7901 (4.33 % ) and otal apoptosis rate (8.1% ) was bigger than control group (4.89%). 150 μg· mL^-1 sasanqua saponin 8 could induce early apoptosis of SGC -7901 (2.46%) and late apoptosis (5.69%). CONCLUSION Sasanqua saponin 7,8 can inhibit the proliferation of SGC - 7901 cells in a dose- independdet manner,and induce apoptosis.
关 键 词:油茶皂素7 油茶皂素8 人胃癌SGC-7901细胞 细胞凋亡
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