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中国癌症防治杂志 ›› 2012, Vol. 4 ›› Issue (2): 153-157.doi: 10.3969/j.issn.1674-5671.2012.02.14

• 肝癌专栏 • 上一篇    下一篇

 重组人血管内皮抑制素对肝癌H22腹水瘤小鼠腹水的抑制作用

  

  1. 广西医科大学附属肿瘤医院化疗五科; 广西医科大学研究生学院
  • 出版日期:2012-06-25 发布日期:2012-07-03
  • 通讯作者: 谢伟敏 E-mail:xieweimin3358@163.com
  • 基金资助:

     广西壮族自治区卫生厅科研课题(Z2009251、Z2009240)

Ability of recombinant human endostatin to reduce H22 ascites in mice

  • Online:2012-06-25 Published:2012-07-03

摘要: 目的 探讨血管内皮抑制素腹腔内给药对H22小鼠腹水瘤生长及腹水的抑制作用。方法 取110只昆明小鼠腹腔内接种H22细胞(2×106细胞/只),建立小鼠腹水瘤模型,接种后随机分为5组:模型对照组(0.9% NS);低剂量血管内皮抑制素组(4mg/kg);中剂量血管内皮抑制素组(8mg/kg);高剂量血管内皮抑制素组(12mg/kg);阳性对照组(顺铂 0.6mg/kg)。接种24h后连续10d给予各药物腹腔内注射,停药24h后处死各组小鼠,测量腹水量并取腹水行相关检测;解剖小鼠,观察腹腔脏器及肺脏的转移情况;通过Evan 蓝的吸光度值反映小鼠的腹膜渗透性;观察各组小鼠的生存时间。结果 与模型对照组相比,中、高剂量血管内皮抑制素组可显著抑制荷H22腹水瘤小鼠腹水的生成,并减少腹腔内及肺脏转移,延长生存时间。结论 血管内皮抑制素腹腔内用药治疗荷H22腹水瘤小鼠腹水具有显著的抑制作用。

关键词:  , 血管内皮抑制素, 血管内皮生长因子, 小鼠, 腹水, 抑制

Abstract: Objective To investigate the effect of intraperitoneal endostar administration to treat H22 ascites in mice. Methods A mouse model of ascites was established by inoculating 110 Kunming mice with H22 cells(2×106,i.p. injection).Mice were then di-vided randomly into 5 groups:control (normal saline);low endostar dose(4 mg/kg•day),intermediate endostar dose(8 mg/kg•day), high endostar dose(12 mg/kg•day)and positive control(DDP 0.6 mg/kg•day).After an adjustment period of 24h,the groups were treated from day 1 to day 10 by i.p. injection as indicated above and sacrificed 24h after drug withdrawal.Data were collected on vol-ume of ascitic fluid,metastases of abdominal organs and lungs and survival time.Peritoneal membrane permeability was assessed us-ing Evan blue staining. Results Intermediate and high doses of endostar significantly inhibited the production of ascites in H22 as-citesbearing mice,reduced the frequency of metastases in the abdominal viscera and lungs,and lengthened average survival time. Conclusion Intraperitoneal administration of endostar can reduce ascites in H22 ascites-bearing mice.

Key words: Endostar, Vascular endothelial growth factor, Mice, Ascites