摘要
目的:阐明扶正抗癌方的抗癌机制。方法:以不同剂量灌胃给药后,不同时间采集大鼠血清、处理体外培养的人肝癌细胞SMMC7721,用MTT法和氚标胸嘧啶掺入法观察细胞增殖能力。结果:扶正抗癌方2次给药后1小时和2小时药物血清处理细胞,MTT转化率和^3H-TdR掺入率明显下降。结论:扶正抗癌方具有明显的抑制人肝癌细胞增殖作用。
Aim: In order to ascertain the anti-carcinoma mechanism of FZKAD. Metheds: FZKAD drug-serum was derived at different time from rats which were orally preadministrated with different-dose FZKAD. The effects of the serum on human hepatoma cells (SMMC7721) were observed by MTT assay and H-TdR incorporating method. Results: After treating with the drug-serum derived at 1h and 2h separately after administrating twice with FZKAD (1. 6g/kg, 8.0g/ kg ), the MTT transformative and 3H-TdR incorporative rate were decreased significantly. Conclusion: FzkaD had remarkable inhibitory effects on proliferation of human hepatoma cells. It might be one of the anticarcinoma mechanisms of FZKAD.
出处
《中西医结合肝病杂志》
CAS
1997年第4期214-216,共3页
Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
基金
上海市教委资助课题
关键词
中药
扶正抗癌方
血清药理学
肝癌
细胞增殖
Fuzheng Kang'ai decoction Serum-pharmacology Human Hepatocarcinoma Cell Proliferation