期刊文献+

干扰素-γ、重组TGF-β1 RII蛋白对小鼠日本血吸虫病肝纤维化的影响

Effects of IFN-γ and rTGF-β1 RⅡ on hepatic fibrosis in mice infected with schistosomiasis japonica
下载PDF
导出
摘要 目的 探讨IFN-γ、重组TGF-β1 RⅡ 蛋白对小鼠日本血吸虫病肝纤维化的影响.方法 昆明小鼠(6~8 周龄,体重18~25g,雌雄各半),随机分成6 组(6 只/组),正常对照组除外,其余30 只通过腹部皮肤感染日本血吸虫尾蚴18依2 条/鼠,六周后成功建立小鼠血吸虫性肝纤维化模型,具体治疗分组:①正常对照组;②模型对照组;③吡喹酮(PQT)治疗组;④PQZ +IFN-γ治疗组;⑤PQT+rTGF-β1RⅡ 蛋白治疗组;⑥PQT+IFN-γ+ rTGF-β1 RⅡ 蛋白治疗组.第九周末处死小鼠,HE 染色法对肝组织进行病理学检查;TBA 法测肝匀浆MDA 含量.结果 IFN-γ、rTGF-β1RⅡ 蛋白治疗显著降低肝纤维化指数,抑制日本血吸虫诱导的肝MDA 水平的升高.结论 日本血吸虫病化学药物治疗中,以PQT 为基础配合rTGF-β1R域蛋白、IFN-γ的联合疗法策略优于PQT 单独用药策略;rTGF-β1R域蛋白、IFN-γ的抗纤维化效应可能与其抗氧化功能有关. Objective To explore the effects of IPN-γ and rTGF-β1RⅡ on hepatic fibrosis in mice infected with schistosomiasis japonica.Methods 36 Kunming mice(6-8 w,body weight 18-22g,male and female in half) were randomly divided into 6 groups(n=6),6 mice were nomal control group,30 mice were challenged percutaneously with 18 ±2 cercariae of Schistosoma japonicum and six weeks later they were randomly divided into 5 groups:model control group,Praziquantel(PQT) group,PQT+IFN-γ group,PQT +rTGF-β1RⅡ group,and PQT+IFN-γ+rTGF-β1RⅡ group.All the mice were killed at the end of the 9th week.The area of egg granuloma and degree of hepatic fibrosis were observed via HE and Masson stainings.The concentrations of liver homogenates MDA were detected by spectrophotometer using Assay Kits.Results IFN-γ and /or TGF-β1RⅡ protein significantly inhibited hepatic collagenous fibrosis in mice infected with schistosomiasis japonicum and reduced the concentrations of MDA that in liver tissue.Conclusion The combination of IFN-γ and sTGF-β1RⅡ with PQT had better effect on hepatic fibrosis in mice infected with schistosomiasis japonica than the single use of PQT.The anti-fibrosis effect of IFN-γ and sTGF-β1RⅡ might relate with its antiantioxidant function.
出处 《热带病与寄生虫学》 2013年第2期71-73,121,共4页 Journal of Tropical Diseases and Parasitology
关键词 日本血吸虫病 Γ-干扰素 重组转化生长因子β1R域型受体 肝纤维化 Schistosomiasis japonica IFN-γ rTGF-β1 RⅡ Hepatic fibrosis
  • 相关文献

参考文献3

二级参考文献14

  • 1Pilling D,Fan T,Huang D,et al.Identification of markers that distinguish monocyte-derived fibrocytes from monocytes,macrophages,and fibroblasts[J].PLoS One,2009,4(10):e7475. 被引量:1
  • 2Yang Y,Yang S,Chen M,et al.Compound Astragalus and Salvia miltiorrhiza extract exerts anti-fibrosis by mediating TGF-beta/Smad signaling in myofibroblasts[J].Ethnopharmacol,2008,118(2):264-70. 被引量:1
  • 3Borkham-Kamphorst E,Herrmann J,Stoll D,et al.Dominant-negative soluble PDGF-beta receptor inhibits hepatic stellate cell activation and attenuates liver fibrosis[J].Lab Invest,2004,84(6):766-77. 被引量:1
  • 4Neil J R,Johnson K M,Nemenoff R A,et al.Cox-2 inactivates Smad signaling and enhances EMT stimulated by TGF-beta through a PGE2-dependent mechanisms[J].Carcinogenesis,2008,29(11):2227-35. 被引量:1
  • 5Peinado H,Quintanilla M,Cano A.Transforming growth factor beta-1 induces snail transcription factor in epithelial cell lines:mechanisms for epithelial mesenchymal transitions[J].Biol Chem,2003,278(23):21113-23. 被引量:1
  • 6Radisky D C,Kenny P A,Bissell M J.Fibrosis and cancer:do myofibroblasts come also from epithelial cells via EMT[J] ? Cell Biochem,2007,101(4):830-9. 被引量:1
  • 7牛丽文,曹琦,李俊,杨镇,王晓红.JAK/STAT途径调节瘦素诱导的肝星状细胞Ⅰ型胶原基因的表达[J].中国药理学通报,2007,23(10):1280-1285. 被引量:13
  • 8金博,李玉彬.肝脏纤维化的诊断对策[J].中华消化杂志,1997,17(3):170-172. 被引量:15
  • 9王锐等编写,赵慰先,高淑芬主编.实用血吸虫病学[M]. 人民卫生出版社, 1996 被引量:1
  • 10Czaja M J,Weiner F R,Flander K S et al.In vitro andin vivo association of transforming growth factor-β1 withhepatic fibrosis[].The Journal of Cell Biology.1989 被引量:1

共引文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部