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Bioengineered Stromal Cell-Derived Factor-1α Analogue Delivered as an Angiogenic Therapy Significantly Restores Viscoelastic Material Properties of Infarcted Cardiac Muscle
Journal article   Open access   Peer reviewed

Bioengineered Stromal Cell-Derived Factor-1α Analogue Delivered as an Angiogenic Therapy Significantly Restores Viscoelastic Material Properties of Infarcted Cardiac Muscle

Alen Trubelja, John W. MacArthur, Joseph J. Sarver, Jeffrey E. Cohen, George Hung, Yasuhiro Shudo, Alexander S. Fairman, Jay Patel, Bryan B. Edwards, Scott M. Damrauer, …
Journal of biomechanical engineering, v 136(8), pp 0845011-0845015
02 Jun 2014
PMID: 24860865
url
https://doi.org/10.1115/1.4027731View
Published, Version of Record (VoR)Open Access (License Unspecified) Open

Abstract

Technical Brief
Ischemic heart disease is a major health problem worldwide, and current therapies fail to address microrevascularization. Previously, our group demonstrated that the sustained release of novel engineered stromal cell-derived factor 1-α analogue (ESA) limits infarct spreading, collagen deposition, improves cardiac function by promoting angiogenesis in the region surrounding the infarct, and restores the tensile properties of infarcted myocardium. In this study, using a well-established rat model of ischemic cardiomyopathy, we describe a novel and innovative method for analyzing the viscoelastic properties of infarcted myocardium. Our results demonstrate that, compared with a saline control group, animals treated with ESA have significantly improved myocardial relaxation rates, while reducing the transition strain, leading to restoration of left ventricular mechanics.

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6 citations in Scopus

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Collaboration types
Domestic collaboration
Web of Science research areas
Biophysics
Engineering, Biomedical
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