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

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

Research output: Contribution to journalArticlepeer-review

3 Scopus 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.

Original languageEnglish
Article number696694
Pages (from-to)265-280
Number of pages16
JournalBiomechanics and Modeling in Mechanobiology
Volume24
Issue number1
DOIs
StatePublished - 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.

FundersFunder 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 Program769-2075
Army’s Institute for Collaborative Biotechnologies UARCCMMI BRITE 2227509, R01HL148785, W911NF-19-2-0026
National Institutes of Health (NIH)CMM1 1662431, 1T32GM141846, RM131981
University of California, Santa BarbaraIRG-2, DMR 2308708
Bill and Melinda Gates FoundationCMMI-CAREER-2048043

    Keywords

    • Heart failure
    • Mechanobiology
    • Stress relaxation
    • Viscoelasticity

    ASJC Scopus subject areas

    • Biotechnology
    • Modeling and Simulation
    • Biomedical Engineering
    • Mechanical Engineering

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