期刊文献+

基质金属蛋白酶3和尿激酶型纤溶酶原激活物受体在2型糖尿病大血管病变中的变化 被引量:7

Changes of matrix metalloproteinase-3 and urokinase-type plasminogen activator receptor in type 2 diabetes mellitus with macroangiopathy
在线阅读 下载PDF
导出
摘要 目的:探讨基质金属蛋白酶3(MMP-3)和尿激酶型纤溶酶原激活物受体(uPAR)在2型糖尿病大血管病变中的变化。方法:用ELISA双抗体夹心法测定26例正常对照和39例2型糖尿病患者(其中单纯2型糖尿病15例、合并大血管病变24例)的血浆MMP-3和uPAR水平。结果:单纯糖尿病组uPAR高于正常对照(P<0.05)而MMP-3无显著差异;合并大血管病变组MMP-3显著高于正常对照和单纯糖尿病组(P<0.01,P<0.01),而uPAR亦高于正常对照及单纯病变组(P<0.01,P<0.05)。2型糖尿病血浆MMP-3水平和uPAR水平呈正相关,LDL-C与uPAR呈正相关且是uPAR主要影响因素。结论:MMP-3和uPAR与2型糖尿病大血管病变发生密切相关,MMP-3可作为2型糖尿病血管病变的循环标志物。 AIM: To investigate the function of matrix metalloproteinase -3 (MMP-3) and urokinase -type plasminogen activator receptor (uPAR) to macroangiopathy in type 2 diabetes mellitus. METHODS: The levels of MMP - 3 and uPAR in plasma were determined by ELISA sandwich method in 26 healthy controls and 39 patients with type 2 diabetes mellitus including 15 complication - free cases and 24 with macroangiopathy. RESULTS : The plasma level of uPAR but not MMP - 3 was higher in patients without macroangiopathy than that in normal controls (P 〈 0. 05 ). In patients with macroangiopathy, the plasma levels of MMP - 3 and uPAR were higher than those in normal controls (P 〈 0. 01 ) and patients without angiopathy. There was positive relationship between MMP - 3 and uPAR in type 2 diabetes mellitus ( r = 0. 405, P 〈0. 05), and LDL - C was the important affecting factor of uPAR. CONCLUSION: MMP - 3 and uPAR are associated with the development of macroangiopathy in type 2 diabetes mellitus. MMP - 3 can be regarded as the circulatory markers in type 2 diabetes mellitus with macroangiopathy.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2007年第5期897-899,共3页 Chinese Journal of Pathophysiology
基金 浙江省卫生厅科学基金资助项目(No.491020-W00602)
关键词 基质金属蛋白酶 受体 尿纤溶酶原激活物 糖尿病 非胰岛素依赖型 动脉硬化 Matrix metalloproteinases Receptors, urinary plasminogen activator Diabetes mellitus, non - insulin - dependent Arteriosclerosis
  • 相关文献

参考文献8

  • 1Dollery CM,McEwan JR,Henney AM.Matrix metalloproteinases and cardiovascular disease[J].Circ Res,1995,77(5):863 -868.
  • 2Steins MB,Padro T,Schwaenen C,et al.Overexpression of urokinase receptor and cell surface urokinase-type plasminogen activator in the human vessel wall with different types of atherosclerotic lesions[J].Blood Coagul Fibrinolysis,2004,15 (5):383-391.
  • 3Herron GS,Banda MJ,Clark EJ,et al.Secretion of metalloproteinases by stimulated capillary endothelial cells.Ⅰ.Production of procollagenase and prostromelysin exceeds expression of proteolytic activity[J].J Biol Chem,1986,261(6):2814 -2818.
  • 4Libby P.Molecular bases of the acute coronary syndromes[J].Circulation,1995,91(11):2844 -2850.
  • 5Uzui H,Harpf A,Liu M,et al.Increased expression of membrane type 3-matrix metalloproteinase in human atherosclerotic plaque:role of activated macrophages and inflammatory cytokines[J].Circulation,2002,106 (24):3024-3030.
  • 6James TW,Wagner R,White LA,et al.Induction of collagenase and stromelysin gene expression by mechanical injury in a vascular smooth muscle -derived cell line[J].J Cell Physiol,1993,157(2):426 -437.
  • 7Rosenberg GA,Navratil M,Barone F,et al.Proteolytic cascade enzymes increase in focal cerebral ischemia in rat[J].J Cereb Blood Flow Metab,1996,16(3):360 -366.
  • 8Kanse SM,Benzakour O,Kanthou C,et al.Induction of vascular SMC proliferation by urokinase indicates a novel mechanism of action in vasoproliferative disorders[J].Arterioscler Thromb Vasc Biol,1997,17 (11):2848 -2854.

同被引文献53

引证文献7

二级引证文献10

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