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中国癌症防治杂志 ›› 2018, Vol. 10 ›› Issue (1): 14-18.doi: 10.3969/j.issn.1674-5671.2018.01.04

• 基础研究 • 上一篇    下一篇

牛磺酸对7,12-二甲基苯蒽诱发大鼠乳腺癌的干预作用及其机制

  

  1. 广西医科大学公共卫生学院营养与食品卫生学教研室
  • 出版日期:2018-02-25 发布日期:2018-03-23
  • 通讯作者: 郭松超 2433164518@qq.com
  • 基金资助:

    广西科技基础条件平台建设资助项目(14-91-02)

Effects of taurine on 7,12-dimethyl benzene [a] anthracene-induced breast cancer in rats and its mechanism of action

  • Online:2018-02-25 Published:2018-03-23

摘要:

目的 研究牛磺酸对7,12-二甲基苯蒽(7,12- dimethyl benzene[a] anthracene,DMBA)诱发大鼠乳腺癌的干预作用及其机制。方法 将30只6周龄雌性SD大鼠随机分为牛磺酸干预组、模型对照组和空白对照组,每组10只。牛磺酸干预组和模型对照组大鼠给予15 mg/100g的DMBA,在牛磺酸干预组的日常饮水中添加3%牛磺酸,一次性灌胃;空白对照组大鼠予1 mL/100 g花生油灌胃。所有大鼠均自由饮水和进食。观察、记录大鼠乳腺肿瘤发生情况,采用酶联免疫吸附试验(enzyme-linked immunosorbent assay,ELISA)检测大鼠血清IL-6和TNF-α含量。结果 与模型对照组相比,牛磺酸干预组肿瘤发生的潜伏期延长,致瘤率、荷瘤总数、血清IL-6和TNF-α水平均下降,差异有统计学意义(P<0.05),肿瘤体积和重量增加,但差异无统计学意义(P>0.05);与空白对照组相比,模型对照组血清IL-6和TNF-α水平显著升高[(41.41±10.10)pg/mL vs (20.00±10.10) pg/mL,P<0.05;(71.72±25.83) pg/mL vs (42.00±16.69) pg/mL,P<0.05),而牛磺酸干预组升高不明显[(22.48±10.38) pg/mL vs(20.00±10.10) pg/mL,P>0.05;(42.52±9.15) pg/mL vs (42.00±16.69)pg/mL,P>0.05)。 结论 牛磺酸对DMBA诱发大鼠乳腺癌的发生有较明显的抑制作用,其机制可能通过调节机体免疫反应途径实现。

关键词: 乳腺肿瘤, 牛磺酸, 7, 12-二甲基苯蒽, 大鼠, 致瘤率, IL-6, TNF-&alpha

Abstract:

Objective  To study the effects of taurine on 7,12-dimethyl benzene [a] anthracene(DMBA)-induced breast cancer in rats and its mechanism of action. Methods A total of 30 male Sprague-Dawley rats were randomly divided into three groups: taurine intervention group,model control group and blank control group. Rats in taurine intervention group  and model control group  were given DMBA (15 mg/100 g) by one-time gavage,while rats in blank control group were given peanut oil (1 mL/100 g). Animals in taurine intervention group  also received 3% taurine in their drinking water. All rats could drink water and eat ad libitum. Levels of IL-6 and TNF-α in serum were measured using enzyme-linked immunosorbent assay (ELISA). Results Compared with model control group ,taurine intervention group  showed a lower rate of tumorigenesis,longer tumor latency,and smaller total number of tumors(P<0.05). Tumor volume and mouse body weight were similar between taurine intervention group and model control group(P>0.05). Levels of serum IL-6 and TNF-α were significantly lower in taurine intervention group  than in model control group(P<0.05),significantly higher in model control group than in blank control group[(41.41±10.10)pg/mL vs (20.00±10.10) pg/mL,P<0.05 ;(71.72±25.83) pg/mL vs (42.00±16.69) pg/mL,P<0.05)],and similar between taurine intervention group and blank control group[(22.48±10.38)pg/mL vs(20.00±10.10) pg/mL,P>0.05;(42.52±9.15) pg/mL vs(42.00±16.69) pg/mL,P>0.05)]. Conclusions Taurine has a significant inhibitory effect on the development of DMBA-induced breast cancer in rats. Taurine may exert these effects by regulating the body's inflammatory and immune responses.

Key words: Breast neoplasms, Taurine, 7, 12-dimethyl benzene[a]anthracene, Rat, Tumorigenic rate, IL-6, TNF-α