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β-咔啉类衍生物对BALB/c裸小鼠肝癌皮下移植瘤生长的影响

张燕 范文玺 徐艺玫 史深 贵友军 燕顺生

实验动物与比较医学2013,Vol.33Issue(4):290-295,6.
实验动物与比较医学2013,Vol.33Issue(4):290-295,6.DOI:10.3969/j.issn.1674-5817.2013.04.009

β-咔啉类衍生物对BALB/c裸小鼠肝癌皮下移植瘤生长的影响

Effect of β-carboline derivative on Subcutaneous Transplant Hepatocellular Carcinoma Growth in BALB/c Nude Mice

张燕 1范文玺 2徐艺玫 1史深 1贵友军 1燕顺生1

作者信息

  • 1. 新疆维吾尔自治区实验动物研究中心,乌鲁木齐830002
  • 2. 新疆华世丹药物研究有限责任公司,乌鲁木齐830000
  • 折叠

摘要

Abstract

Objective To investigate the effect of (a)-carboline derivative HMD on subcutaneous transplant hepatocellular carcinoma in BALB/c nude mice.Methods A tumor model of human HCC was created by subcutaneous inoculation of 2 × 107 (cells/ml,0.2ml) HepG2 cells into BALB/c male nude mice.The mice were randomized to low-(0.22 mg/kg),medium-(0.44 mg/kg),and high-dose HMD (0.87 mg/kg)group,saline group and 5-Fu group.The mice in each group received iv injection of the drug for 15 days.The effects of HMD on the growth of human hepatocellular carcinoma,the weight and pathological changes of nude mice£§S main organs were observed.Results Compared with saline group,the mice in HMD groups and 5-Fu group showed significant inhibition in the growth of the transplanted tumor (P<0.01).The inhibitory rate of HMD on the mouse weight.Compared to the saline group,the inhibitory effects of HMD(0.44,0.87 mg/kg) were of statistic significance (P<0.01).Contrast to the negative control,there were no significant difference to the weight of kidney and kidney index in HMD groups and 5-Fu group,but there were significant differeces in the weight of liver and liver index (P<0.05).Conclusion HMD exhibit an inhibitory effect on the growth of transplanted HepG2 tumor,and the mice don't appear toxicity symptom.

关键词

β-咔啉类衍生物(HMD)/BALB/c裸小鼠/人肝癌皮下移植瘤/急性毒性实验

Key words

β-carboline derivatives(HMD)/ BALB/c nude mice/ Subcutaneous transplanted liver tumor/Acute toxicity

分类

生物科学

引用本文复制引用

张燕,范文玺,徐艺玫,史深,贵友军,燕顺生..β-咔啉类衍生物对BALB/c裸小鼠肝癌皮下移植瘤生长的影响[J].实验动物与比较医学,2013,33(4):290-295,6.

基金项目

新疆维吾尔自治区公益性科研院所基本科研业务经费资助项目(KY2012084) (KY2012084)

实验动物与比较医学

OACSTPCD

1674-5817

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