期刊文献+

慢性肝病患者血清MMP-9 TIMP-1的检测及临床意义 被引量:2

The Change of Serum Matrix Metalloproteinase-9 and tissue inhibitor metalloproteinase-1 in chronic liver disease
在线阅读 下载PDF
导出
摘要 目的 研究基质金属蛋白酶 -9(MMP -9)、基质金属蛋白酶组织抑制因子 -1(TIMP-1)在慢性肝病患者肝纤维化过程中的表达和动态变化。方法 用酶标法检测75例慢性乙型病毒性肝炎和40例乙肝后肝硬化患者血清中MMP -9和TIMP -1的浓度。结果血清MMP-9和TIMP -1浓度在慢性肝病患者肝纤维化过程中逐渐升高 ,与正常对照组比较有显著性意义 (P<0.01) ;其中轻度患者的MMP-9与中度、重度、肝硬化之间 ,肝硬化与中度、重度之间两两比较有显著性差异 (P<0.05或P<0.01) ;除了慢性乙肝重度患者的TIMP -1与肝硬化之间比较无意义外 ,其余各组之间两两比较均有显著性差异 (P<0.01)。结论 血清MMP -9和TIMP -1在慢性肝病患者肝纤维化过程中可能起促进作用 ,能够被用来做为判断肝纤维化程度的指标。 Objective To investigate the dynamic change and expression of Matrix Metalloproteinase-9(MMP-9)and tissue inhibitor metalloproteinase-1(TIMP-1)in patients with chronic hepatiecs B(CHB)and liver cirrhosis(LC). Methods serum MMP-9and TIMP-1were deˉtected by ELISA in 75 patients with CHB and 40 patients with LC and20healthy people. Results (1)serum MMP-9and TIMP-1leveles increased in CHB and LC.there were remarkably significant between patients with chronic liver disease and control group(p<0.01).MMP-9levels in severe degrees of CHB and LC were higher than in mild and moderate of CHB(p<0.05/0.01).and serumMMP-9levels in LC were notably higher than in severe degrees of CHB too.(2)seurm TIMP-1 increased successively in mild,moderate and severe degrees of CHB and LC(p<0.01),besides there were no significiant difference between two groups in severe degrees of CHB and LC(p>0.05). Conclution serum MMP-9 and TIMP-1 leveles increase in CHB and LC.They might participate in the development of hepatic fibrosis and can be used as diagnostic indexes for hepatic fibrosis in chronic liver diseases.
出处 《浙江临床医学》 2004年第3期183-184,共2页 Zhejiang Clinical Medical Journal
关键词 血清 MMP-9 TIMP-1 基质金属蛋白酶-9 基质金属蛋白酶组织抑制因子-1 慢性乙肝 肝硬化 Matrix Metalloproteinase-9 tissue inhibitor metalloproteinase-1 hepatic fibrosis
  • 相关文献

参考文献7

二级参考文献27

  • 1赵静波,王泰龄,张道明,张晶.嗜酒者肝脏病变的形态学研究[J].中华病理学杂志,1994,23(1):14-16. 被引量:21
  • 2[1]Matrisian LM. The matrix- degrading metalloproteinases [J].Bioessays, 1992, 14:455-463.
  • 3[2]Takino T, Sato H, Shinagawa A, et al. Identification of the second membrane- type matrix metalloproteriaiesgene from a human placente cDNA[J]. J Biol Chem, 1995, 270:23013 - 23020.
  • 4[3]Murawaki Y, Ikuta Y, Kawasaki H. Serum matrix metalloproteinawe-1 in patients with chronic viral hepatitis[J] .J Gastroenterol Hepatol, 1999, 14(2):138- 145.
  • 5[4]Murawaki Y, Ikuta Y, Idobe Y, et al. Tissue inhibitor of metalloproteinase - 1 in the liver of patients with chronic liver disease[ J]. J Hepatol, 1997, 26(6): 1213 - 1219.
  • 6[5]Murawaki Y, Ikuta Y, Okamoto K. Serum matrix metalloproteinase - 3 (stromelysin - 1 ) concentration in patients with chronic liver disease[J] .J Hepatol, 1999, 31(3) :474- 481.
  • 7[6]Kasahara A, Hayashi N, Mochizuki K, et al. Circulating matrix metalloproteinase - 2 and tissue inhibitor of metalloproteinase- 1 as serum markers of fibrosis in patients with chronic hepatitis C Relationship to interferon response[ J]. J Hepatol, 1997, 26(3 ): 574 -583.
  • 8[7]Nakamura - T, Ushiyama - C, Suzuki - S. Effect of plasma exchange on serum tissue inhibitor of metalloproteinase 1 and cytokine concentrations in patients with fulminant hepatitis[J]. Blood Purif,2000, 18(11):50-54.
  • 9Davis BH.Transforming growth factor beta responsiveness is mediated by the extracellular, collagen matrix during hepatic Ito cell culture. Journal of Cellular Physiology . 1988
  • 10Ruoslahti E,Integrins. The Journal of Clinical Investigation . 1991

共引文献75

同被引文献44

引证文献2

二级引证文献6

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