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Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

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The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
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Related Experiment Video

Updated: Dec 28, 2025

Echocardiography-guided Injection for Targeted and Reliable Intramyocardial Stem Cell Delivery in a Rat Model of Myocardial Infarction
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Intramyocardial Injections to De-Stiffen the Heart: A Subject-Specific in Silico Approach.

Yaghoub Dabiri1,2, Kevin L Sack1,3, Semion Shaul1

  • 1Department of Surgery, University of California San Francisco, San Francisco, California, USA.

Molecular & Cellular Biomechanics : MCB
|February 18, 2020
PubMed
Summary

Minimally invasive injections of softening agents can globally de-stiffen the left ventricle (LV). Strategic regional myocardial softening effectively reduces LV stiffness, improving function in heart failure models.

Keywords:
HFpEFfinite element modelinginjection treatmentmyocardiumsubject-specific

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Area of Science:

  • Biomedical Engineering
  • Cardiovascular Research
  • Computational Biology

Background:

  • Stiff myocardium in the left ventricle (LV) impairs cardiac function.
  • Current treatments for LV stiffness are limited.
  • Minimally invasive approaches are needed to address myocardial stiffness.

Purpose of the Study:

  • To investigate if targeted injections of a softening agent can globally de-stiffen the left ventricle (LV).
  • To utilize physics-based models to design and optimize regional myocardial softening strategies.
  • To explore this approach for potential treatment of heart failure with preserved ejection fraction (HFpEF).

Main Methods:

  • Constructed physics-based finite element models of the LV using echocardiography and pressure data from swine.
  • Simulated intramyocardial injections of a softening agent at various locations and volumes.
  • Analyzed the impact of regional de-stiffening on global LV mechanics, including end-diastolic volume (EDV).

Main Results:

  • Regional myocardial de-stiffening led to global LV de-stiffening.
  • Injections into the free wall (8 ml) increased EDV by 15.0%; injections into septum and free wall (11 ml) increased EDV by 26.0%.
  • Endocardial injections resulted in EDV comparable to mid-wall and greater than epicardial injections, despite lower volume.

Conclusions:

  • In silico planning of regional myocardium de-stiffening can globally soften a stiff LV.
  • This subject-specific, minimally invasive strategy shows promise for treating HFpEF.
  • Further hypothesis-testing in animal models is warranted to validate simulation findings.