Key result
Infarct MVO regions show increased inflammation and reduced capillary density and collagen versus non-MVO regions.
Why the study?
Microvascular obstruction after myocardial infarction negatively impacts ventricular remodeling, but the extracellular matrix composition at regions of microvascular obstruction remained to be described.
Does microvascular obstruction alter the extracellular matrix composition in reperfused myocardial infarction in a swine model?
Does microvascular obstruction alter the extracellular matrix composition in reperfused myocardial infarction in a swine model?
Microvascular obstruction in reperfused myocardial infarction is associated with increased inflammation and altered extracellular matrix composition, which may drive adverse ventricular remodeling.
MVO-linked ECM changes may drive remodeling in swine MI; leaves open translation to human postinfarct therapies.
BACKGROUND: Extracellular matrix (ECM) suffers substantial alterations after myocardial infarction (MI), including the invasion of leukocyte subtypes. Despite a complete reopening at epicardial level, hypoperfusion within the infarcted myocardium, known as microvascular obstruction (MVO), occurs and exerts a negative impact on ventricular remodeling. In this study, ECM composition at MVO regions was described using a morphometric analysis. METHODS: MI was induced in female swine (n = 10) by transitory 90-minute coronary occlusion followed by seven days of reperfusion. Prior to euthanasia, intracoronary thioflavin-S was infused. Within the infarcted myocardium, regions displaying MVO (thioflavin-S-) or no MVO (thioflavin-S+) were isolated and stained to morphometrically compare ECM composition. RESULTS: As reflected by cell invasion through ECM, areas with MVO displayed an enlarged presence of neutrophils and lymphocytes, whilst no differences in the amount of macrophages and myofibroblasts were detected compared to infarcted myocardium without MVO. Indeed, those regions with macroscopic MVO showed lower capillary density than areas without MVO. Lastly, a significant reduction in the extension of total collagen, type I, but not type III, collagen, laminin, and fibronectin together with an augmentation of polysaccharides were noted in areas showing MVO compared to those without microvascular injury. CONCLUSIONS: ECM composition in infarcted regions with MVO isolated from female swine displays a higher presence of inflammatory infiltrate and polysaccharides as well as reduced number of microvessels and collagen content compared to those areas without microvascular hypoperfusion. These characteristics might underlie the development of adverse ventricular remodeling in MI patients with extensive MVO.
No takes yet. Share an insight, caveat, or question.
Bujeda et al. (2023) studied Myocardial infarction (n=10). Microvascular obstruction (MVO) vs. Infarcted myocardium without MVO was evaluated on Extracellular matrix composition. Microvascular obstruction regions in infarcted myocardium showed increased inflammatory infiltrates and polysaccharides, and reduced capillary density and collagen compared to regions without MVO.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: