癌变·畸变·突变 ›› 2007, Vol. 19 ›› Issue (1): 29-032.doi: 10.3969/j.issn.1004-616x.2007.01.009

• 论著 • 上一篇    下一篇

绿茶对微囊藻毒素LR诱导肝细胞凋亡、Bcl-2表达及骨髓嗜多染红细胞微核的影响

许 川1;舒为群1;邱志群1;常晓松1;罗教华1;付文娟1;曹 佳2   

  1. 1. 第三军医大学军事预防医学院环境卫生学教研室; 2.第三军医大学军事预防医学院卫生毒理学教研室,重庆 400038)
  • 收稿日期:2006-09-04 修回日期:2006-09-04 出版日期:2007-01-30 发布日期:2007-01-30

Effect of Green Tea on Microcystin-LR-induced Hepatocelluar Apoptosis, Bcl-2 Expression and Micronucleus

XU Chuan1, SHU Wei-qun1, QIU Zhi-qun1, CHANG Xiao-song1, LUO Jiao-hua1, FU Wen-juan1, CAO Jia2   

  1. 1. Department of Environmental Hygiene;2. Department of Hygiene Toxicology,School of Military Preventive Medicine, The Third Military Medical University, Chongqing 400038,China)
  • Received:2006-09-04 Revised:2006-09-04 Online:2007-01-30 Published:2007-01-30

摘要: 背景与目的: 研究绿茶(green tea,GT)对微囊藻毒素LR(MC-LR)诱导肝细胞凋亡、Bcl-2蛋白表达及微核发生的影响以探讨毒性拮抗机制。 材料与方法: 雄性小鼠50只随机分为5组,分别为空白对照、MC-LR染毒组、GT高低剂量拮抗组和环磷酰胺对照组。实验第1 d起GT高、低剂量拮抗组小鼠每日分别给予12 g/L和2 g/L两种浓度的GT自由饮用,连续18 d。自第6 d开始,染毒小鼠每日给予MC-LR 10 μg/kg腹腔注射1次,空白对照给予DMSO腹腔注射,连续13 d。环磷酰胺对照组以50 mg/kg剂量间隔24 h两次给药后6 h取材。小鼠处死后采用免疫组化和计数法对肝细胞凋亡、Bcl-2蛋白表达以及骨髓嗜多染红细胞(PCEs)微核发生率进行检测和分析。结果: (1) MC-LR染毒明显诱导小鼠肝细胞凋亡增加。高剂量GT处理后明显抑制MC-LR染毒所致小鼠肝细胞凋亡的发生(P<0.05);(2) 单纯MC-LR染毒肝细胞Bcl-2表达未见明显变化,GT各剂量组小鼠肝脏Bcl-2的表达明显增加,与MC-LR染毒组相比差异具有统计学意义(P<0.01)。(3) GT拮抗组小鼠骨髓嗜多染红细胞微核率(PCEs-MN) 与MC-LR染毒对照和空白对照相比,其差异均无统计学意义(P>0.05)。结论: GT能上调抑癌基因Bcl-2的表达,抑制细胞凋亡。MC-LR染毒及GT拮抗对微核发生均未有显著影响。

关键词: 绿茶, 微囊藻毒素LR, 凋亡, Bcl-2, 微核

Abstract: BACKGROUND & AIM: To evaluate the effects of green tea (GT) on Microcystin-LR (MC-LR)-induced hepatocelluar apoptosis, Bcl-2 expression and micronucleus test so as to explore antagonistic mechanism of GT. MATERIALS AND METHODS: 50 male mice were randomly divided into five groups. Mice in GT pretreated groups were given green tea as free drink at doses of 2 g/(L·d) and 12 g/(L·d) prior to MC-LR intoxication, consecutively for 18 days. The toxin treatment mice in group MC-LR control received continual intraperitoneal injections of MC-LR at dose of 10 μg/(kg·d) for 13 days from day 6 till sacrifice. CP control group was treated with intraperitoneal cyclophosphamide twice at dose of 50 mg/(kg·d) 24 h interval on days 17 and 18. Mice were sacrificed and immediately subjected to autopsy. Hepatocellular apoptosis, Bcl-2 protein expression and micronucleus frequencies of bone marrow were evaluated immediately. RESULTS: (1) MC-LR induced obvious hepatocellular apoptosis. High dose of GT pretreatment significantly inhibited MC-LR-induced hepatocellular apoptosis(P<0.05).(2) There was no significant change of Bcl-2 protein expression in MC-LR control compared with control. As compared with only MC-LR, the expression of Bcl-2 protein was significantly increased in GT pretreatment groups(P<0.01).(3) No significant difference in micronucleus frequencies was found in either MC-LR control or GT pretreatment groups compared with control (P>0.05). CONCLUSION: GT could increase Bcl-2 protein expression and inhibit hepatocellular apoptosis,MC-LR and GT pretreatment did not cause damage to mice chromosome.

Key words: green tea, microcystin-LR, apoptosis, bcl-2, micronucleus

中图分类号: