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Updated: Sep 23, 2026

Murine Myocardial Infarction Model using Permanent Ligation of Left Anterior Descending Coronary Artery
Published on: August 16, 2019
Time-dependent changes in the plasma concentration of matrix metalloproteinase 9 after acute myocardial infarction
Jens J Kaden1, Carl-Erik Dempfle, Tim Sueselbeck
11st Department of Medicine (Cardiology, Angiology and Pulmonology), University Hospital of Mannheim, Mannheim, Germany. jens.kaden@med.ma-uni-heidelberg.de
Abstract:
Matrix metalloproteinase (MMP)-2 and MMP-9 are believed to play a pathophysiologic role in acute myocardial infarction (MI). The time course of their plasma concentrations in correlation with the extent of myocardial damage is unclear. In a prospective study, 20 patients with proven acute MI underwent successful reperfusion within 6 h after the onset of symptoms. The patients were divided into two groups according to the size of their MI, i.e. large or moderate MI. Plasma concentrations of MMP-2, MMP-9 and tissue inhibitor of metalloproteinase (TIMP)-1 were determined on admission, and after 24 h, 48 h, 1 week, 4 weeks, 3 months and 6 months. MMP-2 levels remained unchanged over time in both groups. The plasma concentration of MMP-9 was elevated on admission in patients with large MI versus moderate MI (195 +/- 190 versus 78 +/- 63 ng/ml, p < 0.01) as determined by left ventriculography, and returned to baseline (18 +/- 16 ng/ml) by 1 week after MI. TIMP-1 levels rose slowly in patients with large MI and returned to baseline at 6 months. The ratio of MMP-9 to TIMP-1 was significantly increased on admission in both groups and returned to baseline at 48 h. These data suggest that MMP-9 might play a pathophysiologic role during the early phase of acute MI.
Insights
Matrix metalloproteinase-9 (MMP-9) levels are elevated in acute myocardial infarction (MI) patients with larger infarcts. MMP-9 may play a key role in the early stages of acute MI.
Area of Science:
- Cardiology
- Biochemistry
- Molecular Biology
Background:
- Matrix metalloproteinases (MMPs), specifically MMP-2 and MMP-9, are implicated in the pathophysiology of acute myocardial infarction (MI).
- The temporal dynamics of MMP plasma concentrations and their relationship to myocardial damage extent remain incompletely understood.
Purpose of the Study:
- To investigate the time course of plasma concentrations of MMP-2, MMP-9, and tissue inhibitor of metalloproteinase-1 (TIMP-1) in patients with acute MI.
- To correlate these concentrations with the size of myocardial infarction.
Main Methods:
- A prospective study involving 20 patients with acute MI who underwent successful reperfusion within 6 hours of symptom onset.
- Patients were stratified into large or moderate MI groups based on left ventriculography.
- Plasma MMP-2, MMP-9, and TIMP-1 levels were measured at multiple time points: admission, 24 hours, 48 hours, 1 week, 4 weeks, 3 months, and 6 months.
Main Results:
- MMP-2 levels showed no significant changes over time in either group.
- Plasma MMP-9 concentrations were significantly higher on admission in patients with large MI compared to moderate MI (195 ± 190 vs. 78 ± 63 ng/ml, p < 0.01).
- MMP-9 levels returned to baseline by 1 week post-MI. TIMP-1 levels increased gradually in the large MI group, returning to baseline at 6 months. The MMP-9/TIMP-1 ratio was elevated on admission in both groups, normalizing by 48 hours.
Conclusions:
- MMP-9 plasma concentrations are elevated early in acute MI, particularly in patients with larger infarcts.
- These findings suggest a potential pathophysiologic role for MMP-9 during the acute phase of myocardial infarction.
- MMP-2 levels do not appear to be significantly altered in the early phase of acute MI in this cohort.
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