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

    Source: Journal of Biomechanical Engineering:;2014:;volume( 136 ):;issue: 008::page 84501
    Author:
    Trubelja, Alen
    ,
    MacArthur, John W.
    ,
    Sarver, Joseph J.
    ,
    Cohen, Jeffrey E.
    ,
    Hung, George
    ,
    Shudo, Yasuhiro
    ,
    Fairman, Alexander S.
    ,
    Patel, Jay
    ,
    Edwards, Bryan B.
    ,
    Damrauer, Scott M.
    ,
    Hiesinger, William
    ,
    Atluri, Pavan
    ,
    Joseph Woo, Y.
    DOI: 10.1115/1.4027731
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: 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 cellderived factor 1خ± 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 wellestablished 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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      Bioengineered Stromal Cell Derived Factor 1خ± Analogue Delivered as an Angiogenic Therapy Significantly Restores Viscoelastic Material Properties of Infarcted Cardiac Muscle

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    http://yetl.yabesh.ir/yetl1/handle/yetl/154054
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    • Journal of Biomechanical Engineering

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    contributor authorTrubelja, Alen
    contributor authorMacArthur, John W.
    contributor authorSarver, Joseph J.
    contributor authorCohen, Jeffrey E.
    contributor authorHung, George
    contributor authorShudo, Yasuhiro
    contributor authorFairman, Alexander S.
    contributor authorPatel, Jay
    contributor authorEdwards, Bryan B.
    contributor authorDamrauer, Scott M.
    contributor authorHiesinger, William
    contributor authorAtluri, Pavan
    contributor authorJoseph Woo, Y.
    date accessioned2017-05-09T01:05:35Z
    date available2017-05-09T01:05:35Z
    date issued2014
    identifier issn0148-0731
    identifier otherbio_136_08_084501.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/154054
    description abstractIschemic 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 cellderived factor 1خ± 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 wellestablished 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.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleBioengineered Stromal Cell Derived Factor 1خ± Analogue Delivered as an Angiogenic Therapy Significantly Restores Viscoelastic Material Properties of Infarcted Cardiac Muscle
    typeJournal Paper
    journal volume136
    journal issue8
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4027731
    journal fristpage84501
    journal lastpage84501
    identifier eissn1528-8951
    treeJournal of Biomechanical Engineering:;2014:;volume( 136 ):;issue: 008
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
    نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
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