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    Contractile Smooth Muscle and Active Stress Generation in Porcine Common Carotids

    Source: Journal of Biomechanical Engineering:;2018:;volume( 140 ):;issue: 001::page 14501
    Author:
    Zhou, Boran
    ,
    Prim, David A.
    ,
    Romito, Eva J.
    ,
    McNamara, Liam P.
    ,
    Spinale, Francis G.
    ,
    Shazly, Tarek
    ,
    Eberth, John F.
    DOI: 10.1115/1.4037949
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: The mechanical response of intact blood vessels to applied loads can be delineated into passive and active components using an isometric decomposition approach. Whereas the passive response is due predominantly to the extracellular matrix (ECM) proteins and amorphous ground substance, the active response depends on the presence of smooth muscle cells (SMCs) and the contractile machinery activated within those cells. To better understand determinants of active stress generation within the vascular wall, we subjected porcine common carotid arteries (CCAs) to biaxial inflation–extension testing under maximally contracted or passive SMC conditions and semiquantitatively measured two known markers of the contractile SMC phenotype: smoothelin and smooth muscle-myosin heavy chain (SM-MHC). Using isometric decomposition and established constitutive models, an intuitive but novel correlation between the magnitude of active stress generation and the relative abundance of smoothelin and SM-MHC emerged. Our results reiterate the importance of stretch-dependent active stress generation to the total mechanical response. Overall these findings can be used to decouple the mechanical contribution of SMCs from the ECM and is therefore a powerful tool in the analysis of disease states and potential therapies where both constituent are altered.
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      Contractile Smooth Muscle and Active Stress Generation in Porcine Common Carotids

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    contributor authorZhou, Boran
    contributor authorPrim, David A.
    contributor authorRomito, Eva J.
    contributor authorMcNamara, Liam P.
    contributor authorSpinale, Francis G.
    contributor authorShazly, Tarek
    contributor authorEberth, John F.
    date accessioned2019-02-28T11:11:30Z
    date available2019-02-28T11:11:30Z
    date copyright11/9/2017 12:00:00 AM
    date issued2018
    identifier issn0148-0731
    identifier otherbio_140_01_014501.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4253648
    description abstractThe mechanical response of intact blood vessels to applied loads can be delineated into passive and active components using an isometric decomposition approach. Whereas the passive response is due predominantly to the extracellular matrix (ECM) proteins and amorphous ground substance, the active response depends on the presence of smooth muscle cells (SMCs) and the contractile machinery activated within those cells. To better understand determinants of active stress generation within the vascular wall, we subjected porcine common carotid arteries (CCAs) to biaxial inflation–extension testing under maximally contracted or passive SMC conditions and semiquantitatively measured two known markers of the contractile SMC phenotype: smoothelin and smooth muscle-myosin heavy chain (SM-MHC). Using isometric decomposition and established constitutive models, an intuitive but novel correlation between the magnitude of active stress generation and the relative abundance of smoothelin and SM-MHC emerged. Our results reiterate the importance of stretch-dependent active stress generation to the total mechanical response. Overall these findings can be used to decouple the mechanical contribution of SMCs from the ECM and is therefore a powerful tool in the analysis of disease states and potential therapies where both constituent are altered.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleContractile Smooth Muscle and Active Stress Generation in Porcine Common Carotids
    typeJournal Paper
    journal volume140
    journal issue1
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4037949
    journal fristpage14501
    journal lastpage014501-6
    treeJournal of Biomechanical Engineering:;2018:;volume( 140 ):;issue: 001
    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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