Evidence map›Paper›PMID 39741200›Full record

ArticleBiomechanics and modeling in mechanobiology2025

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 and 1 more

Abstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 3D Bioprinting Functional Engineered Heart Tissues.International journal of molecular sciences · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Marissa Gionet-GonzalesBioengineering, University of California, Santa Barbara, Santa Barbara, United States.
Gianna GathmanBioengineering, University of California, Santa Barbara, Santa Barbara, United States.
Jonah RosasMaterials, University of California, Santa Barbara, Santa Barbara, United States.
Kyle Y KunisakiMechanical Engineering, University of California, Santa Barbara, Santa Barbara, United States.
Dominique Gabriele P InocencioMechanical Engineering, University of California, Santa Barbara, Santa Barbara, United States.
Niki HakamiMechanical Engineering, University of California, Santa Barbara, Santa Barbara, United States.
Gregory N MilburnInternal Medicine, University of Kentucky, Lexington, United States.
Angela A PitenisMaterials, University of California, Santa Barbara, Santa Barbara, United States.
Kenneth S CampbellInternal Medicine, University of Kentucky, Lexington, United States.
Beth L PruittBioengineering, University of California, Santa Barbara, Santa Barbara, United States. blp@ucsb.edu.
Ryan S StowersBioengineering, University of California, Santa Barbara, Santa Barbara, United States. rstowers@ucsb.edu.

Funding

From proteins to cells to tissues: A multi-scale assessment of biomechanical regulation by the myosin molecular motorRM1GM131981 · NIGMS · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL, MACK, DAVID LEE · 2019 to 2023
$10.3M
NRSA Training CoreTL1TR001997 · NCATS · UNIVERSITY OF KENTUCKY · PI PENDERGAST, JULIE S, STOOPS, WILLIAM WALTON · 2016 to 2025
$4.2M
Dual filament control of myocardial power and hemodynamicsR01HL148785 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI Kenneth S Campbell, Thomas Kampourakis · 2020 to 2026
$3.2M
Length-dependent activation in human myocardiumR01HL149164 · NHLBI · UNIVERSITY OF KENTUCKY · PI CAMPBELL, KENNETH S, TANNER, BERTRAND C.W. · 2020 to 2023
$2.8M
Predoctoral Training Program in Quantitative MechanobiologyT32GM141846 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI Siddharth Subhas Dey, Beth L Pruitt · 2021 to 2026
$1.9M
U-RISE at UC MercedT34GM145511 · NIGMS · UNIVERSITY OF CALIFORNIA, MERCED · PI MICHELE Kiyoko NISHIGUCHI, Rudy M Ortiz · 2022 to 2026
$1.6M
American Heart Association 24POST1195931Bill and Melinda Gates Foundation Gates Millennium ScholarshipInstitute for Collaborative Biotechnologies W911NF-19-2-0026National Science Foundation 769-2075National Science Foundation CMMI 1662431National Science Foundation CMMI-CAREER-2048043NCATS NIH HHS TL1 TR001997NHLBI NIH HHS R01 HL148785NHLBI NIH HHS R01 HL149164NIGMS NIH HHS RM1 GM131981NIGMS NIH HHS T32 GM141846NIGMS NIH HHS T34 GM145511NIH HHS 1T32GM141846NIH HHS 1T32GM145511-01NIH HHS R01HL148785NIH HHS RM1GM131981
6 · The paper itself

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.

Indexed as

Heart FailureMyocardiumStress, MechanicalAgedAnimalsBiomechanical PhenomenaElasticityFemaleFibrosisHeart VentriclesHumansMaleMiddle AgedPericardiumSwineViscosityHeart failureMechanobiologyStress relaxationViscoelasticity

Identifiers

PMID39741200
PMCPMC11846740

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.