期刊文献+

蚯蚓提取物对肝纤维化大鼠α-SMA、TGFβ1、uPA及PAI-1蛋白表达的影响 被引量:3

Effects of earthworm 2 on the expressions of α-SMA、TGFβ_1、uPA and PAI-1 in hepatic fibrosis rat
下载PDF
导出
摘要 目的研究蚯蚓提取物地龙2号对实验性大鼠肝纤维化的α肌动蛋白(αSMA)、转化生长因子β1(TGFβ1)、尿激酶型纤溶酶原激活物(uPA)及Ⅰ型纤溶酶原激活抑制物(PAI1)蛋白表达的影响。方法52只雄性Wistar大鼠,随机分成6组:正常组(N);阴性对照组(NC),皮下注射花生油,灌单蒸水;模型组(M),皮下注射CCl4,每日单蒸水灌胃;阳性对照组(PC),造模同时用秋水仙碱0.1mg·kg-1·d-1灌胃;地龙大剂量组(Eh),造模同时用地龙2号50mg·kg-1·d-1灌胃;地龙小剂量组(El),造模同时用地龙2号25mg·kg-1·d-1灌胃。8周末处死大鼠,用免疫组化法检测各组大鼠肝脏组织中αSMA、TGFβ1、uPA及PAI1的表达情况。结果地龙2号大、小剂量组与模型组相比,αSMA、TGFβ1、uPA及PAI1的表达均显著降低,且uPA、PAI1与αSMA及TGFβ1表达下降呈明显的正相关。结论地龙2号可能通过抑制肝纤维化大鼠肝组织中肝星状细胞的活化,降低TGFβ1、uPA及PAI1的表达,发挥抗肝纤维化作用。 Objective To investigate the effects of earthworm extractions (E2) on the expressions of α-SMA,uPA,TGFβ_1 and PAI-1 of hepatic fibrosis in rats. Methods Fifty-two male Wistar rats were randomly divided into six groups:normal group (N), normal control group (NC), model group (M), positive control group (PC), high dose of E2 group (Eh) and low dose of E2 group (El). The rats in group of M, PC, Eh and El were subcutaneously injected with CCl_4 for 8 weeks to induce liver fibrosis, and the rats in group NC were injected with peanut oil only.Group PC rats were administrated with colchicine. Rats in group Eh and El were administrated with different dose of E2. At the end of 8 weeks,all survived rats were sacrificed humanely, liver specimens were preserved in 10% buffered paraformaldehyde and dehydrated in a graded alcohol series. Following xylene treatment, the specimens were embedded in paraffin blocks and cut continuously into 4μm thick sections, and the expressions of α-SMA,TGFβ_1,uPA and PAI-1 were observed by immunohistochemistry technique.Results Compared to those in model group, the expressions of α-SMA,TGFβ_1,uPA and PAI-1 in animals of groups Eh and El were significantly lower and the decrease of uPA and PAI-1 was obviously positively correlated with that of α-SMA and TGFβ_1 in groups Eh and El. Conclusion E2 can inhibit obviously the formation of liver fibrosis induced by CCl_4 in rats, which may be relateed to inhibiting the activation of hepatic stellate cells and decreasing the proteinic expressions of TGFβ_1,uPA and PAI-1.
出处 《江苏医药》 CAS CSCD 北大核心 2005年第6期443-445,F003,共4页 Jiangsu Medical Journal
基金 江苏省中医药管理局科研项目(Z019)
  • 相关文献

参考文献5

二级参考文献32

  • 1潘雪飞,张长法,邱蔚蔚,吕国强,周明伟,常洁,倪颖,李圣青,韩停琴.慢性肝病患者血清层粘蛋白及透明质酸的变化[J].新消化病学杂志,1996,4(7):373-374. 被引量:39
  • 2Oikawa T, Freeman M, Lo W, et al. Modulation of plasminogen activator inhibitor-1 in vivo: a new mechenisrn for the anti-fibrotie effect of renin-angiotensin inhibition. Kidney Int, 1997, 51: 164-172.
  • 3Sisson T, Hattori N, Xu Y, et al. Treatment of blemycin-induced pulmonary fibrosis by transfeyr of urokinase-type plasminogen activator genes. Hum Gene Ther, 1999, 10:2315-2323.
  • 4Shimizu M, Hara A, Okuno M, et al. Mechanima of retarded liver regeneration in plasminogen actlvator-deficlent mice. impaired activation of hepatocyte growth factor after Fas-medinated massive hepatic apotosis. Hepatology, 2001, 33:569-576.
  • 5Salgado S, Garcia Y, Vera J, et al. Liver cirrosis is reverted by urokinase-type plasrninogen activator gene hterapy. Mol Ther, 2000,2:545-551.
  • 6Berkrnpas M, Quigley J. Transformation-dependent activation of urokinase-type plasminogen activator by a plasmin independent mechanism: involvement of cell surface membranes. Proc nat Acad Sci,1999, 88:7768-7772.
  • 7Ossowski L, Clonie G, Masucci M,. et al. In vivo paracine interaction between urokinase and its receptor: effect on tumor cell invasion. J Cell Biol. 1999, 115:1107-1112.
  • 8Clark E, Brugge J. Integrins and signal transduction pathways. Science, 1995, 268:233-239.
  • 9Myohanen H, Stephens R, Hedman K, et al. Distribution and lateral mobility of the urokinase-reeeptor complex at the cell surface. J Histochem Cytochem, 1993, 41:1291-1301.
  • 10Bugge T, Suh T, Flick M, et al. The receptor ofor urolinase-type plasminogen activator is not essential for mouse development or fertility.J Biol Chain, 1995, 270:16886-16894.

共引文献59

同被引文献75

引证文献3

二级引证文献11

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