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Published on: October 12, 2017
Diet-Induced Hypercholesterolemia Leads to Cardiac Dysfunction and Alterations in the Myocardial Proteome
Márton Richárd Szabó1,2, Márton Pipicz1,2, Márta Sárközy1,2
1Department of Biochemistry, Albert Szent-Györgyi Medical School, University of Szeged, H-6720 Szeged, Hungary.
Insights
High cholesterol damages the heart by altering cardiac proteins. This study found hypercholesterolemia disrupts cytoskeletal and mitochondrial proteins, potentially causing heart dysfunction.
Area of Science:
- Cardiovascular Biology
- Proteomics
- Molecular Cardiology
Background:
- Elevated blood cholesterol is a significant risk factor for coronary heart disease.
- Hypercholesterolemia can directly impact heart muscle function (myocardium).
Purpose of the Study:
- To investigate the effects of induced hypercholesterolemia on the cardiac proteome.
- To identify specific protein expression changes in the heart linked to high cholesterol.
Main Methods:
- Male Wistar rats were fed a cholesterol-supplemented diet for 8 weeks to induce hypercholesterolemia.
- Proteomic analysis of left ventricular tissue was performed.
- Gene Ontology (GO) and protein interaction analyses were applied to the data.
Main Results:
- Hypercholesterolemia was associated with diastolic dysfunction in rats.
- Altered expression of 45 proteins was identified in hypercholesterolemic hearts.
- Downregulation of cytoskeletal proteins (e.g., beta-actin) and contractile proteins (e.g., troponins, myosin) was observed.
- Subunits of the mitochondrial respiratory chain were also downregulated.
Conclusions:
- Hypercholesterolemia significantly alters the cardiac proteome.
- Changes in cytoskeletal, contractile, and mitochondrial proteins may underlie the development of diastolic dysfunction in hypercholesterolemia.
Abstract:
Elevated blood cholesterol is a major risk factor for coronary heart disease. Moreover, direct effects on the myocardium also contribute to the adverse effects of hypercholesterolemia. Here, we investigated the effect of hypercholesterolemia on the cardiac proteome. Male Wistar rats were fed with a laboratory rodent chow supplemented with 2% cholesterol for 8 weeks to induce hypercholesterolemia. The protein expression data obtained from the proteomic characterization of left ventricular samples from normo- and hypercholesterolemic animals were subjected to gene ontology (GO) and protein interaction analyses. Elevated circulating cholesterol levels were accompanied by diastolic dysfunction in cholesterol-fed rats. The proteomic characterization of left ventricular samples revealed altered expression of 45 proteins due to hypercholesterolemia. Based on the Gene Ontology analysis, hypercholesterolemia was associated with disturbed expression of cytoskeletal and contractile proteins. Beta-actin was downregulated in the hypercholesterolemic myocardium, and established a prominent hub of the protein interaction network. Analysis of the unfiltered dataset revealed concordant downregulated expression patterns in proteins associated with the arrangement of the contractile system (e.g., cardiac-specific troponins and myosin complex), and in subunits of the mitochondrial respiratory chain. We conclude that the observed changes in the cardiac proteome may contribute to the development of diastolic dysfunction in hypercholesterolemia.
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