癌变·畸变·突变 ›› 2006, Vol. 18 ›› Issue (5): 370-373.doi: 10.3969/j.issn.1004-616x.2006.05.010

• 论著 • 上一篇    下一篇

α-生育酚琥珀酸酯抗小鼠Ehrlich氏腹水癌作用的研究

李红卫1,2/吴 坤2,   

  1. 1.厦门大学医学院预防医学系,福建 厦门361005;2.哈尔滨医科大学公共卫生学院营养与食品卫生教研室,黑龙江 哈尔滨 150086
  • 收稿日期:2005-11-21 修回日期:2006-05-29 出版日期:2006-09-30 发布日期:2006-09-30
  • 通讯作者: 吴 坤

Antineoplastic Effects of α-Tocopheryl Succinate in Ehrlich Ascitesocarcinoma Bearing Mice

LI Hong-wei1,2, WU Kun2,   

  1. 1.Department of Preventive Medicine, Medical College, Xiamen University, Xiamen Fujian 365001, China; 2. Department of Nutrition and Food Hygiene, School of Public Health, Harbin Medical University, Heilongjiang 150001, China
  • Received:2005-11-21 Revised:2006-05-29 Online:2006-09-30 Published:2006-09-30
  • Contact: WU Kun

摘要: 背景与目的: 研究α-生育酚琥珀酸酯(α-Tocopheryl succinate,α-TOS)抑制实验动物体内肿瘤的生长作用,并探讨其作用机制。 材料与方法: 建立Ehrlich氏腹水癌小鼠实验动物模型,设阴性对照组、肿瘤模型对照组、α-TOS实验组(20、40和80 mg/kg)和环磷酰胺对照组,观察α-TOS对Ehrlich氏腹水癌小鼠生存期的延长作用,检测各实验组动物血液学指标、NK细胞活性、T细胞亚群,应用DNA琼脂糖凝胶电泳检测α-TOS诱导肿瘤细胞凋亡的作用。 结果: 80 mg/kg剂量组α-TOS对Ehrlich氏腹水癌小鼠的生命延长率达33.09%;α-TOS各实验组白细胞(WBC)含量明显高于环磷酰胺阳性对照组,血小板(PLT)含量低于瘤模型对照组;40和80 mg/kg α-TOS两剂量组NK细胞活性明显高于肿瘤模型对照组(P<0.05, P<0.01);α-TOS各实验组T细胞亚群数值接近于阴性对照组;在80 mg/kg剂量下α-TOS处理的Ehrlich氏腹水癌小鼠腹水细胞中检测到明显的DNA梯度(Ladder)。 结论: α-TOS可延长Ehrlich氏腹水癌小鼠的生存时间,减轻荷瘤小鼠因血小板增多引起的血液粘稠状态,且无降低白细胞的副作用;增强荷瘤小鼠NK细胞杀伤活性、纠正T淋巴细胞亚群异常,缓解和改善荷瘤小鼠免疫力低下和免疫紊乱状态,激发机体免疫系统并在抑制肿瘤生长过程中发挥作用,并且α-TOS可诱导Ehrlich氏腹水癌小鼠腹水癌细胞凋亡。

关键词: α-生育酚琥珀酸酯, Ehrlich氏腹水癌, 抗肿瘤作用

Abstract: BACKGROUND & AIM: To study the inhibiting effects of α-tocopheryl succinate(α-TOS) on the growth of Ehrlich ascitesocarcinoma in vivo and explore the mechanisms. MATERIAL AND METHODS: The mice loaded with Ehrlich ascitesocarcinoma were used as tumor model, all the experimental animals were divided into negative control, tumor model, α-TOS treatment at dose 20, 40 and 80 mg/kg and cyclophosphamide positive groups. The survival ratio of tumor-bearing mice and subsequent hematological changes were measured, NK cytotoxicity and the proportion of T lymphocyte subsets were detected by lactate dehydrogenase method and Flow Cytometer, respectively. Inducibility of Ehrlich cell apoptosis was examined by DNA agarose gel electrophoresis. RESULTS: The survival ratio in α-TOS treatment group at dose 80 mg/kg was 33.09%. The white blood cell counts in α-TOS treatment groups were much higher than in positive control, the platelet counts were much lower than in tumor model. The NK cytotoxicity became much higher in α-TOS treatment groups at dose 40 and 80 mg/kg compared with the tumor model(P<0.05 and P<0.01). The T lymphocyte subset counts were close to negative control in α-TOS treatment groups. The DNA ladder was found in Ehrlich ascitesocarcinoma cells at dose 80 mg/kg. CONCLUSION: α-TOS was capable of prolonging the survival time of mice with Ehrlich ascitesocarcinoma; could alleviate hyperviscosity caused by the increase in the number of platelets, without interfering with the number of leucocytes; was able to activate immune system in the process ofinhibiting the growth of tumor due to improved immune function. The result of DNA agarose gel electrophoresis demonstrated that α-TOS induced apoptosis of Ehrlich ascitesocarcinoma cells at a dose of 80mg/kg.

Key words: α-Tocopheryl succinate, Ehrlich ascitesocarcinoma, antineoplastic effect