食品科学 ›› 2013, Vol. 34 ›› Issue (11): 278-284.

• 营养卫生 • 上一篇    下一篇

低氘白酒对人肺腺癌细胞抑制作用的实验研究

张亚茹,丛峰松   

  1. 上海交通大学生命科学技术学院
  • 收稿日期:2012-02-13 修回日期:2013-05-02 出版日期:2013-06-15 发布日期:2013-06-03
  • 通讯作者: 丛峰松 E-mail:fscong@sjtu.edu.cn

The research of inhibition effect of Deuterium-Depleted-alcohol on lung cancer A549 and H460

2   

  • Received:2012-02-13 Revised:2013-05-02 Online:2013-06-15 Published:2013-06-03

摘要:

目的:探讨低氘白酒在体内外对肺腺癌的抑制作用。方法:在体外,采用MTT法检测白酒、低氘水(DDW)和低氘白酒(DDA)抑制人肺癌A549细胞的增殖情况;采用TUNEL法和流式细胞仪分别检测白酒、DDW和DDA诱导人肺癌A549细胞的凋亡率。在体内,建立肺癌移植瘤模型,造模当日给药。9 d后,开始测量瘤体生长曲线。21 d后,断颈处死小鼠,称量体重及瘤重,固定小鼠瘤组织及肝肺组织,HE染色检测病理变化。结果:在体外,72h,180 mM DDA能明显抑制A549增殖, 抑制率为29.42±2.73%,与空白组及白酒组相比较,具有显著性差异,p<0.05;TUNEL法检测A549细胞凋亡率,表明:DDA能促进细胞凋亡,与空白组,DDW组,白酒组相比较,具有显著性差异,p<0.05;FCM法检测到DDA能促进细胞凋亡。在体内,DDA组与DDW组肿瘤抑制率分别为31.014%和27.639 %,与空白组相比较,具有显著性差异,p<0.05。HE染色结果显示,DDW组与DDA低剂量组,肿瘤细胞排列松散,周围有坏死组织。同时,DDW及DDA对裸鼠的肝肺组织无影响。结论:低剂量DDA在体外能抑制肺腺癌A549细胞增殖,在体内能抑制人肺腺癌H460裸鼠皮下移植瘤生长,并诱导癌细胞凋亡。

关键词: 低氘水, 低氘白酒, 抗肿瘤效应

Abstract:

[Abtract] Objective: To observe the inhibition of the deuterium-depleted-alcohol on the proliferation of lung cancer cell A549 and H460. Methods: In vitro, the inhibition effects of alcohol, deuterium-depleted water (DDW) and deuterium-depleted-alcohol (DDA) on the proliferation of lung cancer cell A549 were measured by MTT assay, and the apoptosis were determined by TUNEL method and flow cytometry. In vivo, human lung cancer H460 cells were inoculated intradermally into nude mice. After 9 days, the growth curve was drawn to show the growing characteristics of xenograft. After 21 days, we sacrificed the mice, weighed and calculated the ratios of tumor-suppression. We also detected the pathological changes of tumor tissues to observe the tumor necrosis degree by HE staining. The pathological changes of the liver and lung tissues were also observed. Results: The proliferation ability of A549 was remarkably inhibited at the concentration of 180 mM of DDA, compared with the control group and the alcohol group(p <0.05); Apoptosis of A549 was remarkably induced by DDA, compared with the control group、the alcohol group and DDW group(p <0.05); Moreover, FCM assay results showed that DDA could promote apoptosis. The in vivo data showed the tumor inhibition rates were higher in DDA and DDW group than that in the control group (p <0.05), 31.014% and 27.639% respectively. HE staining showed that tumor cells necrosed and arranged loosely in DDA and DDW group, and no obvious changes in lung and liver tissue had been observed. Conclusion: DDA has evident inhibition effect on the proliferation of lung cancer cell.

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