Related Experiment Video
Updated: Oct 26, 2025

Murine Myocardial Infarction Model using Permanent Ligation of Left Anterior Descending Coronary Artery
Published on: August 16, 2019
Dystrophin and metalloproteinase 9 in myocardial ischemia: A post-mortem immunohistochemical study
Cristina Mondello1, Elvira Ventura Spagnolo2, Giovanni Bartoloni3
1Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, via Consolare Valeria, 1, 98125 Messina, Italy.
Insights
Sudden cardiac death (SCD) due to coronary atherosclerotic disease (CAD) involves changes in dystrophin and MMP-9. Loss of dystrophin appears to be an early indicator of myocardial ischemia, aiding post-mortem diagnosis.
Area of Science:
- Cardiovascular Pathology
- Forensic Pathology
- Biomarker Research
Background:
- Coronary atherosclerotic disease (CAD) is a leading cause of sudden cardiac death (SCD).
- Accurate post-mortem diagnosis of myocardial ischemia is crucial in forensic investigations.
- The expression patterns of specific proteins during ischemia are not fully elucidated.
Purpose of the Study:
- To evaluate dystrophin and MMP-9 expression in SCD cases related to CAD.
- To analyze the chronological expression of these proteins for diagnostic utility.
- To compare dystrophin and MMP-9 expression with C5b-9 complex and fibronectin.
Main Methods:
- Immunohistochemical staining was performed on myocardial tissue samples.
- Samples were categorized into two groups based on histological evidence of ischemia and a control group.
- Expression levels of dystrophin, MMP-9, C5b-9, and fibronectin were assessed.
Main Results:
- Dystrophin and MMP-9 exhibited distinct expression patterns between groups with and without histological signs of ischemia.
- Group 1 showed sarcolemmal staining depletion for dystrophin and increased interstitial/granulocyte positivity for MMP-9.
- Loss of dystrophin staining and C5b-9 positivity were more pronounced than MMP-9 increases.
Conclusions:
- Dystrophin and MMP-9 are potential immunohistochemical markers for detecting myocardial ischemic damage.
- Loss of dystrophin expression may serve as an earlier marker of myocardial ischemia compared to MMP-9.
- These findings can aid in the post-mortem diagnosis of myocardial ischemia in SCD cases.
Abstract:
The presented study evaluated the expression of dystrophin and MMP-9 in cases of sudden cardiac death (SCD) due to coronary atherosclerotic disease (CAD) in order to analyze the characteristics and the chronology of their expression, providing evidence on the possible role in post-mortem diagnosis of myocardial ischemia. The expression of these proteins was also compared to C5b-9 complex and fibronectin expression to evaluate any differences. Two groups of CAD-related SCD, respectively group 1 with gross and/or histological evidence and group 2 with no specific histological signs of myocardial ischemia, were used. A third group formed by cases of acute mechanical asphyxiation was used as a control. The immunohistochemical staining by dystrophin, MMP-9, C5b-9, and fibronectin antibodies was performed. The study revealed that dystrophin and MMP-9 showed different expression in group 1 and group 2 as, respectively, different degree of sarcolemmal staining depletion and increasing of interstitial and granulocytes immunopositivity. Moreover, loss of dystrophin staining and C5b-9 immunopositivity were more significant when compared to MMP-9 increasing. Dystrophin and MMP-9 seemed to be useful immunohistochemical markers for the detection of myocardial ischemic damage. However, the comparison of the four markers suggested that loss of dystrophin could be considered as an earlier marker.
Related Concept Videos
Myocarditis I: Introduction
Blood Studies for Cardiovascular System I: Cardiac Biomarkers
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...

