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DESCRIPTION (provided by applicant): Cardiac arrhythmias arise from abnormalities of either impulse propagation (reentry-based) or impulse initiation (focal or ectopic). The development of reentry arrhythmias, which involves rotation of an excitation wave around an anatomical or functional block, was observed both in vitro and in vivo and conceptually is well understood. In contrast, our comprehension of ectopic (non-reentrant) arrhythmias has a major gap. To gain initial insights into this process we propose to use a range of available models of cardiac tissue (both experimental and theoretical) in which infarct-like area will be created. Our preliminary studies have revealed that development of ectopic arrhythmias proceeds via an essential step, which we named an ectopic nexus (EN) It refers to a functional state of an injured cardiac tissue in which multiple poorly-coupled ectopic sources form a transient "breeding" microenvironment in which ectopic activity develops from individual cells into slowly propagating ectopic waves confined to the area of injury. The waves of excitation from surrounding healthy tissue fail to invade the EN, allowing slow ectopic waves to co-exist side-by-side with normal propagation pattern. Subsequent relief of EN conditions results in an escape of the ectopic waves leading to an arrhythmia. The EN is a novel concept, which, if it does occur in vivo, has important implications for both understanding and clinical treatment of arrhythmias and ventricular fibrillation. However, experimental and theoretical models employed in our previous studies had several limitations and the relevance of the EN concept to in vivo arrhythmias needs to be further established. Specifically, one needs to know whether EN is limited to 2D cultures of cardiac cells or to a specific set of experimental conditions, how electrical activity match data obtained using calcium transients, whether the EN occurs in a 3D environment, and many other questions. The goal of this application is to provide answers to these questions in order to establish a pathophysiological significance of EN.
期刊论文(15)
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会议论文
DOI: 10.1016/j.tox.2010.09.007
发表时间: 2011-01-11
期刊: TOXICOLOGY
影响因子: 4.5
作者: [Posnack, Nikki Gillum, Lee, Norman H., Brown, Ronald, Sarvazyan, Narine]
通讯作者: Sarvazyan, Narine
DOI: 10.1109/tbme.2011.2143713
发表时间: 2011-07
期刊: IEEE transactions on bio-medical engineering
影响因子: --
作者: [Asfour H, Swift LM, Sarvazyan N, Doroslovački M, Kay MW]
通讯作者: Kay MW
DOI: 10.1158/0008-5472.can-10-1169
发表时间: 2010-09-01
期刊: Cancer research
影响因子: 11.2
作者: [House CD, Vaske CJ, Schwartz AM, Obias V, Frank B, Luu T, Sarvazyan N, Irby R, Strausberg RL, Hales TG, Stuart JM, Lee NH]
通讯作者: Lee NH
Evolution of spiral and scroll waves of excitation in a mathematical model of ischaemic border zone.
缺血边界区域数学模型中的螺旋和滚动波的演变。
DOI: 10.1371/journal.pone.0024388
发表时间: 2011
期刊: PloS one
影响因子: 3.7
作者: [Biktashev VN, Biktasheva IV, Sarvazyan NA]
通讯作者: Sarvazyan NA
9
    New generation of catheters for treatment of atrial fibrillation
    Cardiomyocyte-derived Venous Assist Device: Aiding peripheral blood flow
    • 批准号:
      8968858
    • 项目类别:
    • 资助金额:
      $19.81万
    • 财政年份:
      2014
    • 负责人:
      NARINE SARVAZYAN
    • 依托单位:
    New generation of catheters for treatment of atrial fibrillation
    Cardiomyocyte-derived Venous Assist Device: Aiding peripheral blood flow
    • 批准号:
      8824058
    • 项目类别:
    • 资助金额:
      $23.38万
    • 财政年份:
      2014
    • 负责人:
      NARINE SARVAZYAN
    • 依托单位:
    海外基金