Stress relaxation rates of myocardium from failing and non-failing hearts

The heart is a dynamic pump whose function is influenced by its mechanical properties. The viscoelastic properties of the heart, i.e., its ability to exhibit both elastic and viscous characteristics upon deformation, influence cardiac function. Viscoelastic properties change during heart failure (HF), but direct measurements of failing and non-failing myocardial tissue stress relaxation under constant displacement are lacking. Further, how consequences of tissue remodeling, such as fibrosis and fat accumulation, alter the stress relaxation remains unknown. To address this gap, we conducted stress relaxation tests on porcine myocardial tissue to establish baseline properties of cardiac tissue. We found porcine myocardial tissue to be fast relaxing, characterized by stress relaxation tests on both a rheometer and microindenter. We then measured human left ventricle (LV) epicardium and endocardium tissue from non-failing, ischemic HF and non-ischemic HF patients by microindentation. Analyzing by patient groups, we found that ischemic HF samples had slower stress relaxation than non-failing endocardium. Categorizing the data by stress relaxation times, we found that slower stress relaxing tissues were correlated with increased collagen deposition and increased α-smooth muscle actin (α-SMA) stress fibers, a marker of fibrosis and cardiac fibroblast activation, respectively. In the epicardium, analyzing by patient groups, we found that ischemic HF had faster stress relaxation than non-ischemic HF and non-failing. When categorizing by stress relaxation times, we found that faster stress relaxation correlated with Oil Red O staining, a marker for adipose tissue. These data show that changes in stress relaxation vary across the different layers of the heart during ischemic versus non-ischemic HF. These findings reveal how the viscoelasticity of the heart changes, which will lead to better modeling of cardiac mechanics for in vitro and in silico HF models.

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Publication Details

Journal
Biomechanics and Modeling in Mechanobiology
Published
2024-12-31
DOI
https://doi.org/10.1007/s10237-024-01909-4
Citations
4
Primary Topic
Elasticity and Material Modeling
Type
article
Field-Weighted Citation Impact
0.74

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article

Stress relaxation rates of myocardium from failing and non-failing hearts

Gregory Milburn, Angela A. Pitenis, Ryan S. Stowers, Kenneth S. Campbell et al.
4 citations
Biomechanics and Modeling in Mechanobiology
Elasticity and Material Modeling
0.74
article

Stress relaxation rates of myocardium from failing and non-failing hearts

Gregory Milburn, Angela A. Pitenis, Ryan S. Stowers, Kenneth S. Campbell, Jonah Rosas, Niki Hakami, Beth L. Pruitt, Gianna Gathman, Dominique Gabriele P. Inocencio, Marissa Gionet-Gonzales, Kyle Y. Kunisaki
article en
4 citations

Abstract

The heart is a dynamic pump whose function is influenced by its mechanical properties. The viscoelastic properties of the heart, i.e., its ability to exhibit both elastic and viscous characteristics upon deformation, influence cardiac function. Viscoelastic properties change during heart failure (HF), but direct measurements of failing and non-failing myocardial tissue stress relaxation under constant displacement are lacking. Further, how consequences of tissue remodeling, such as fibrosis and fat accumulation, alter the stress relaxation remains unknown. To address this gap, we conducted stress relaxation tests on porcine myocardial tissue to establish baseline properties of cardiac tissue. We found porcine myocardial tissue to be fast relaxing, characterized by stress relaxation tests on both a rheometer and microindenter. We then measured human left ventricle (LV) epicardium and endocardium tissue from non-failing, ischemic HF and non-ischemic HF patients by microindentation. Analyzing by patient groups, we found that ischemic HF samples had slower stress relaxation than non-failing endocardium. Categorizing the data by stress relaxation times, we found that slower stress relaxing tissues were correlated with increased collagen deposition and increased α-smooth muscle actin (α-SMA) stress fibers, a marker of fibrosis and cardiac fibroblast activation, respectively. In the epicardium, analyzing by patient groups, we found that ischemic HF had faster stress relaxation than non-ischemic HF and non-failing. When categorizing by stress relaxation times, we found that faster stress relaxation correlated with Oil Red O staining, a marker for adipose tissue. These data show that changes in stress relaxation vary across the different layers of the heart during ischemic versus non-ischemic HF. These findings reveal how the viscoelasticity of the heart changes, which will lead to better modeling of cardiac mechanics for in vitro and in silico HF models.

Biomechanics and Modeling in MechanobiologyVol. 24(1)
University of Kentucky (US), University of California, Santa Barbara (US)
National Science Foundation, Bill and Melinda Gates Foundation, American Heart Association, National Institutes of Health, Institute for Collaborative Biotechnologies
Good health and well-being
Openalex Percentile: Top 31%
Elasticity and Material Modeling
0.74
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