Plasma monitoring of the myocardial specific tissue inhibitor of metalloproteinase-4 after alcohol septal ablation in hypertrophic obstructive cardiomyopathy

被引:16
作者
Stroud, RE
Deschamps, AM
Lowry, AS
Hardin, AE
Mukherjee, R
Lindsey, ML
Ramamoorthy, S
Zile, MR
Spencer, WH
Spinale, FG
机构
[1] Med Univ S Carolina, Div Cardiothorac Surg, Charleston, SC 29403 USA
[2] Ralph H Johnson Vet Assoc Med Ctr, Charleston, SC USA
关键词
hypertrophy; TIMP-4; HOCM; alcohol-induced myocardial infarction;
D O I
10.1016/j.cardfail.2004.05.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The overall goal of this study was to develop an assay procedure for measuring the relative abundance of tissue inhibitor of metalloproteinase (TIMP)-4 in plasma, and then use this approach to determine dynamic changes of TIMP-4 levels in hypertrophic obstructive carchomyopathic (HOCM) patients after an acute myocardial infarction (MI). Matrix metalloproteinases (MMPs) contribute to tissue remodeling and are regulated by the endogenous TIMPs. TIMP-4 is observed to be expressed in higher abundance in the myocardium when compared with other types of tissues. Recent clinical studies have measured changes in TIMP-4 levels; however, these studies have been limited to measuring this protein from myocardial tissue samples. To date, no studies have monitored TIMP-4 levels in plasma samples. Methods and Results: Plasma TIMP-4 levels were examined (by semiquantitative immunoblotting) in normal (n = 18) and HOCM (n = 16) patients after alcohol-induced MI. Serial measurements of plasma TIMP-4 levels were examined up to 60 hours after alcohol-induced MI in patients with HOCM. Unglycosylated plasma TIMP-4 levels increased 250% in the HOCM patients when compared with normal controls. Total plasma TIMP-4 levels decreased by 20% at 30 hours after alcohol-induced MI. Conclusions: The unique results demonstrated that an induction of a controlled MI, specifically through alcohol ablation, caused a reduction in plasma TIMP-4 levels in HOCM patients after alcohol-induced MI that would facilitate myocardial remodeling in the early post-MI setting.
引用
收藏
页码:124 / 130
页数:7
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