中国寄生虫学与寄生虫病杂志 ›› 2005, Vol. 23 ›› Issue (6): 14-443.

• 实验报道 • 上一篇    下一篇

小鼠感染日本血吸虫后肝组织Bcl-2、Bax的表达及己酮可可碱对它的作用

魏屏,罗端德,熊莉娟,曾令兰

  

  1. 华中科技大学同济医学院附属协和医院传染科,武汉 430022
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2005-12-30 发布日期:2005-12-30

Expression of Hepatic Bcl-2 and Bax Proteins in Schistosome-InfectedMice and the Role of Pentoxifylline

WEI Ping,LUO Duan-de,XIONG Li-juan,ZENG Ling-lan   

  1. Department of Infectious Diseases,Union Hospital,Tong Ji Medical College,Hua Zhong University of Science and Technology,Wuhan 430022,China
  • Received:1900-01-01 Revised:1900-01-01 Online:2005-12-30 Published:2005-12-30

摘要: 目的 观察凋亡相关基因Bcl?鄄2、Bax在小鼠感染血吸虫后肝组织中的表达情况及己酮可可碱(pentoxi-fylline,PTX)对其作用。 方法 将40只小鼠随机分为4组,其中3组每只小鼠人工感染日本血吸虫尾蚴25条,1组感染后继续喂养10周,不作治疗,作为感染对照组;2组分别于感染后2周用PTX 360 mg/(kg·d)和180 mg/(kg·d)灌胃治疗8周;另1组不感染、也不接受药物治疗,与上述3组同步喂养10周,作为正常对照组。10周后将上述4组小鼠分别剖杀取肝组织,光镜观察肝组织病变;用免疫组化染色方法检测小鼠肝组织中Bcl-2、Bax的水平。 结果 感染对照组中Bcl?鄄2和Bax的表达水平较正常对照组明显增加(P<0.05)。高剂量PTX治疗组Bcl-2水平明显高于低剂量PTX治疗组和感染对照组(P<0.05)。而Bax的表达水平在感染对照组、低剂量PTX治疗组、高剂量PTX治疗组等3组间差异无统计学意义(P>0.05)。同时高剂量PTX治疗组肝组织变性坏死及纤维化程度较低剂量PTX治疗组和感染对照组轻。 结论 高剂量PTX可能通过促进Bcl-2表达,减少肝细胞的变性坏死,阻断血吸虫肝纤维化的发生。

关键词: 日本血吸虫, Bcl-2, Bax, 己酮可可碱

Abstract: Objective To study the expression of hepatic Bcl-2 and Bax proteins in mice infected with Schistosoma japonicum and the role of pentoxifylline (PTX) in the expression. Methods Forty mice were randomly divided into 4 groups: one normal control group,mice in the other three groups were all infected each with 25 cercariae, the infected control group was fed for 10 weeks after infection, and 2 weeks after infection, the high dose PTX group was given PTX 360 mg/(kg·d) for 8 weeks and the low dose PTX group was given PTX 180 mg/(kg·d)also for 8 weeks. At the end of 10 weeks all the mice were killed. Bcl-2 and Bax proteins expression was detected by immunohistochemisty. Results Compared with the normal control group, the expression of Bcl-2 and Bax was significantly higher in the infected control group (P﹤0.05). Bcl-2 was significantly higher in high dose PTX group than in the infected control group and in low dose PTX group (P﹤0.05). However there was no significant difference in the expression of Bax among the groups (P﹥0.05). Conclusion PTX treatment can significantly increase the expression of Bcl-2 in liver tissue of schistosome-infected mice in a dose-dependent manner, and may play a role against liver inflammation and schistosomiasis-related liver fibrosis.

Key words: Schistosoma japonicum, Bcl-2, Bax, Pentoxifylline(PTX)