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.
| Original language | English |
|---|---|
| Article number | 696694 |
| Pages (from-to) | 265-280 |
| Number of pages | 16 |
| Journal | Biomechanics and Modeling in Mechanobiology |
| Volume | 24 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 2025 |
Bibliographical note
Publisher Copyright:© The Author(s) 2024.
Funding
MGG acknowledges funding from American Heart Association (DOI https://doi.org/10.58275/AHA.24POST1195931.pc.gr.190777 ), National Science Foundation (NSF) (ID 769-2075), and the Presidents Postdoctoral Fellowship Program. G.G. acknowledges support from the National Institutes of Health (NIH 1T32GM141846). This work was additionally supported by NIH grant RM131981, as well as funding from the NSF (CMM1 1662431). Rheological data was acquired through the MRL Shared Experimental Facilities, which are supported by the MRSEC Program of the NSF under Award No. DMR 2308708; a member of the NSF-funded Materials Research Facilities Network (www.mrfn.org). Microindenter supplies and consumables used in this work were partially supported by the NSF Materials Research Science and Engineering Center (MRSEC) at UC Santa Barbara through DMR-2308708 (IRG-2). J.M.R. acknowledges academic year support from the Gates Millennium Scholarship through the Bill and Melinda Gates Foundation and Hispanic Scholarship Fund and summer support from the NSF CAREER Award (CMMI-CAREER-2048043). A.A.P. acknowledges summer support from the NSF CAREER Award (CMMI-CAREER-2048043) and from the Army’s Institute for Collaborative Biotechnologies UARC Contract W911NF-19-2-0026). K.S.C. and G.N.M. acknowledge support from NIH R01HL148785. B.L.P. acknowledges funding from NSF CMMI BRITE 2227509.
| Funders | Funder number |
|---|---|
| American the American Heart Association | |
| Materials Research Science and Engineering Center, University of Nebraska-Lincoln | |
| Materials Research Science and Engineering Center, Harvard University | |
| National High Technology Development Program of China (863 Program) | |
| NSF-funded | |
| National Science Foundation Arctic Social Science Program | 769-2075 |
| Army’s Institute for Collaborative Biotechnologies UARC | CMMI BRITE 2227509, R01HL148785, W911NF-19-2-0026 |
| National Institutes of Health (NIH) | CMM1 1662431, 1T32GM141846, RM131981 |
| University of California, Santa Barbara | IRG-2, DMR 2308708 |
| Bill and Melinda Gates Foundation | CMMI-CAREER-2048043 |
Keywords
- Heart failure
- Mechanobiology
- Stress relaxation
- Viscoelasticity
ASJC Scopus subject areas
- Biotechnology
- Modeling and Simulation
- Biomedical Engineering
- Mechanical Engineering