云南中医学院学报
雲南中醫學院學報
운남중의학원학보
JOURNAL OF YUNNAN COLLEGE OF TRADITIONAL CHINESE MEDICINE
2013年
4期
17-20
,共4页
郑永仁%吴德松%王礴%周铭涛%杨和金
鄭永仁%吳德鬆%王礴%週銘濤%楊和金
정영인%오덕송%왕박%주명도%양화금
升麻总苷%抗肿瘤活性%细胞周期
升痳總苷%抗腫瘤活性%細胞週期
승마총감%항종류활성%세포주기
total glycoside of Cimicifuga foetida L.%anti-tumor activity%cell cycle
目的研究升麻总苷提取物(Total Glycoside of Cimicifuga foetida,TGC)的体内、外抗肿瘤活性及其对人肿瘤细胞周期分布的影响。方法 MTT法检测TGC对人肿瘤细胞株的增殖抑制活性;体内实验观察TGC对小鼠肝癌H22移植瘤和人肝癌裸小鼠异种移植瘤Bel-7402的抑制作用;荧光染色法和流式细胞仪检测其对肿瘤细胞周期的影响。结果 TGC可明显抑制人肝癌HepG2细胞的增殖,其IC50值为(76.16±2.94) mg·L-1;TGC 0.8 g·kg-1剂量可明显抑制小鼠肝癌H22和人肝癌Bel-7402裸小鼠移植瘤的生长;TGC 50 mg·L-1可明显诱导人肝癌HepG2细胞阻滞于G2/M 期,呈现出一定的时-效关系。结论 TGC具有明显的体内、外抗肿瘤作用,其活性可能与阻滞肿瘤细胞周期有关。
目的研究升痳總苷提取物(Total Glycoside of Cimicifuga foetida,TGC)的體內、外抗腫瘤活性及其對人腫瘤細胞週期分佈的影響。方法 MTT法檢測TGC對人腫瘤細胞株的增殖抑製活性;體內實驗觀察TGC對小鼠肝癌H22移植瘤和人肝癌裸小鼠異種移植瘤Bel-7402的抑製作用;熒光染色法和流式細胞儀檢測其對腫瘤細胞週期的影響。結果 TGC可明顯抑製人肝癌HepG2細胞的增殖,其IC50值為(76.16±2.94) mg·L-1;TGC 0.8 g·kg-1劑量可明顯抑製小鼠肝癌H22和人肝癌Bel-7402裸小鼠移植瘤的生長;TGC 50 mg·L-1可明顯誘導人肝癌HepG2細胞阻滯于G2/M 期,呈現齣一定的時-效關繫。結論 TGC具有明顯的體內、外抗腫瘤作用,其活性可能與阻滯腫瘤細胞週期有關。
목적연구승마총감제취물(Total Glycoside of Cimicifuga foetida,TGC)적체내、외항종류활성급기대인종류세포주기분포적영향。방법 MTT법검측TGC대인종류세포주적증식억제활성;체내실험관찰TGC대소서간암H22이식류화인간암라소서이충이식류Bel-7402적억제작용;형광염색법화류식세포의검측기대종류세포주기적영향。결과 TGC가명현억제인간암HepG2세포적증식,기IC50치위(76.16±2.94) mg·L-1;TGC 0.8 g·kg-1제량가명현억제소서간암H22화인간암Bel-7402라소서이식류적생장;TGC 50 mg·L-1가명현유도인간암HepG2세포조체우G2/M 기,정현출일정적시-효관계。결론 TGC구유명현적체내、외항종류작용,기활성가능여조체종류세포주기유관。
Objective To investigate the anti-tumor activity of total glycoside of Cimicifuga foetida L.(TGC) and its mechanism. Methods The growth inhibitory effect of TGC on human hepatoma cell line HepG2 was observed by using assay(MTT);In vivo anti-tumor activity of TGC were evaluated in transplant hepatoma H22 model and human hepatocellular carcinoma Bel-7402 xenograft nude mice model;Cell cycle distribution was assayed by flow cytometry. Results TGC could markedly inhibit the growth of HepG2 (IC50=76.16 ±2.94 mg·L-1). Compared with the solvent group,TGC showed a significant inhibitory effect on H22 and Bel-7402 at a dose of 0.8 g·kg-1. Furthermore,TGC could arrest HepG2 at G2/M phase at a concentration of 50 mg·L-1 in a time-dependent manner. Conclusion TGC had significant anti-tumor effects both in vivo and in vitro,which might be associated with the arresting of the tumor cell cycle at G2/M phase.