癌变·畸变·突变 ›› 2007, Vol. 19 ›› Issue (5): 392-394.doi: 10.3969/j.issn.1004-616x.2007.05.013

• 论著 • 上一篇    下一篇

平调饮抗肿瘤作用的实验研究

高晋生/ 宋爱英/ 毕俊芳/ 高 磊   

  1. (黑龙江中医药大学,黑龙江 哈尔滨 150040)
  • 收稿日期:2006-07-27 修回日期:2007-04-02 出版日期:2007-09-30 发布日期:2007-09-30
  • 通讯作者: 高晋生

Experimental Study on Anti_tumor Effects of Pingtiaoyin

GAO Jin_sheng,SONG Ai_ying,BI Jun_fang,GAO Lei   

  1. (Heilongjiang Chinese Traditional Medical University,Haerbin 150040,China)
  • Received:2006-07-27 Revised:2007-04-02 Online:2007-09-30 Published:2007-09-30
  • Contact: GAO Jin_sheng

摘要: 背景与目的: 建立H22肝癌腹水瘤荷瘤小鼠模型,通过给予模型鼠平调饮灌胃评价其抗肿瘤作用。 材料与方法: 用H22腹水肝癌株种植于小鼠右腋皮下,致移植性肿瘤,建立H22肝癌腹水瘤荷瘤小鼠模型。将模型鼠分成阴性对照组,平调饮组,平调饮+5_Fu组和5_Fu组,共4组,各组模型鼠分别灌胃生理盐水、平调饮、平调饮+5_Fu和5_Fu,连续灌胃10 d后,观察瘤体大小、胸腺指数、脾脏指数、抑瘤率、生命延长率和VEGF在肿瘤及肿瘤周围组织中的表达。 结果: 平调饮组肿瘤平均瘤体、VEGF值减小,胸腺指数、脾脏指数、抑瘤率(48.6%)及生命延长率(168.3%)增高。 结论: 平调饮可提高胸腺指数,降低5_Fu对免疫功能的毒性作用,显著延长荷瘤小鼠的生存期。平调饮可能通过促进肿瘤细胞分化成熟,抑制肿瘤细胞增殖,降低肿瘤组织和肿瘤周围组织中VEGF表达,而对H22腹水型小鼠肿瘤的发展起抑制作用。

关键词: 平调饮, H22肝癌腹水瘤荷瘤小鼠, 血管内皮生长因子(VEGF), 抗肿瘤

Abstract: BACKGROUND & AIM: To establish a model of mouse hepatoma H22 and to study the effects of Pingtiaoyin on the tumor. MATERIALS AND METHODS: The model of transplanted tumor was made by vaccination of hepatoma H22 in the right axilla.The model mice were divided into 4 groups:0.9% NaCl,Pingtiaoyin,Pingtiaoyin+5_Fu and 5_Fu.The diameter of transplanted tumor, inhibition rates,thymus and spleen indexes,the rates of life prolongation and the expression of VEGF in carcinoma and peri_carcinoma tissues were analyzed. RESULTS: The diameter of the tumor and the expression of VEGF in the carcinoma were reduced, thymus and spleen indexes,the inhibition rates and the life prolongation rates were increased after treatment with Pingtiaoyin. CONCLUSION: Pingtiaoyin could improve the thymus index,reduce the negative effect of 5_Fu on the immune function, and prolong the survival of the model mouse. Pingtiaoyin also could inhibit the growth of transplanted tumor in mouse through increasing the differentiation of carcinoma cells,reducing their proliferation and downregulating the expression of VEGF in carcinoma and pre_carcinoma tissues.

Key words: pingtiaoyin, mouse hepatoma H22, vascular endothelial growth factor (VEGF), anti_tumor

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