Imbalance of Matrix Metalloproteinases/Tissue Inhibitor of Metalloproteinase-1 and Loss of Fibronectin Expression in Patients with Congestive Heart Failure

被引:22
作者
Yang, Da-chun [1 ]
Ma, Shuang-tao [1 ]
Tan, Yan [1 ]
Chen, Yi-hua [2 ]
Li, De [1 ]
Tang, Bing [1 ]
Chen, Jin-song [1 ]
Su, Xiao-hua [1 ]
Li, Gang [1 ]
Zhang, Xin [1 ]
Yang, Yong-jian [1 ]
机构
[1] PLA Chengdu Mil Area Command, Gen Hosp, Dept Cardiol, Chengdu 610083, Peoples R China
[2] PLA Chengdu Mil Area Command, Gen Hosp, Dept Pathol, Chengdu 610083, Peoples R China
关键词
Myocardial remodeling; Valvular heart disease; Extracellular matrix; MESSENGER-RNA EXPRESSION; MYOCARDIAL-INFARCTION; EXTRACELLULAR-MATRIX; TISSUE INHIBITOR; UP-REGULATION; RAT MODEL; MMP-9; REPERFUSION; PROGRESSION; BALANCE;
D O I
10.1159/000317245
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Previous studies have demonstrated that an imbalance of matrix metalloproteinases (MMPs)/tissue inhibitors of metalloproteinase-1 (TIMP-1) and a loss of fibronectin are associated with postmyocardial infarction remodeling in rats. The present study was designed to examine this issue in patients with congestive heart failure (CHF). Methods: We measured plasma levels and the cardiac protein expression of MMPs/TIMP-1 and fibronectin in 39 patients with CHF and 38 controls. Results: Plasma levels of MMP-2, MMP-3, and MMP-9 tended to be higher in patients with CHF (NYHA II: 276 +/- 18, 613 +/- 118, and 245 +/- 43 mu g/l, respectively; NYHA III: 302 +/- 20, 850 +/- 132, and 310 +/- 39 mu g/l, respectively; NYHA IV: 367 +/- 15, 998 +/- 99, and 392 +/- 27 mu g/l, respectively) than in controls (213 +/- 23, 485 +/- 102, and 158 +/- 31 mu g/l, respectively), while the plasma TIMP-1 level tended to be lower in patients with CHF (NYHA II: 126 +/- 12 mu g/l, NYHA III: 83 +/- 11 mu g/l, and NYHA IV: 61 +/- 12 mu g/l) than in controls (208 +/- 15 mu g/l). Interestingly, the changes in protein expression of MMPs/TIMP-1 were consistent with their plasma concentration. Furthermore, the fibronectin level in the patients with CHF was significantly lower than in the controls. Conclusions: These data suggest that human CHF is associated with an imbalance of MMPs/TIMP-1 and a concurrent loss of fibronectin. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:133 / 141
页数:9
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