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首页> 外文期刊>Journal of applied physiology >Dynamic left ventricular elastance: a model for integrating cardiac muscle contraction into ventricular pressure-volume relationships
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Dynamic left ventricular elastance: a model for integrating cardiac muscle contraction into ventricular pressure-volume relationships

机译:动态左心室弹性:将心肌收缩整合到心室压力-容积关系中的模型

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摘要

To integrate myocardial contractile processes into left ventricular (LV) function, a mathematical model was built. Muscle fiber force was set equal to the product of stiffness and elastic distortion of stiffness elements, i.e., force-bearing cross bridges (XB). Stiffness dynamics arose from recruitment of XB according to the kinetics of myofilament activation and fiber-length changes. Elastic distortion dynamics arose from XB cycling and the rate-of-change of fiber length. Muscle fiber stiffness and distortion dynamics were transformed into LV chamber elastance and volumetric distortion dynamics. LV pressure equaled the product of chamber elastance and volumetric distortion, just as muscle-fiber force equaled the product of muscle-fiber stiffness and lineal elastic distortion. Model validation was in terms of its ability to reproduce cycle-time-dependent LV pressure response, Delta P(t), to incremental step-like volume changes, Delta V, in the isolated rat heart. All Delta P(t), regardless of the time in the cycle at which Delta P(t) was elicited, consisted of three phases: phase 1, concurrent with the leading edge of Delta V; phase 2, a brief transient recovery from phase 1; and phase 3, sustained for the duration of systole. Each phase varied with the time in the cycle at which Delta P(t) was elicited. When the model was fit to the data, cooperative activation was required to sustain systole for longer periods than was possible with Ca2+ activation alone. The model successfully reproduced all major features of the measured Delta P(t) responses, and thus serves as a credible indicator of the role of underlying contractile processes in LV function.
机译:为了将心肌收缩过程整合到左心室(LV)功能中,建立了数学模型。肌纤维力设置为等于刚度和刚度元素的弹性变形的乘积,即,承载力的跨桥(XB)。根据肌丝活化和纤维长度变化的动力学,XB募集产生了刚度动力学。弹性变形动力学是由XB循环和纤维长度的变化率引起的。肌肉纤维的刚度和变形动力学转化为左室弹性和体积变形动力学。左心室压力等于室弹性和体积变形的乘积,就像肌纤维力等于肌纤维刚度和线性弹性变形的乘积一样。模型验证是根据其在离体大鼠心脏中对增量的阶梯状体积变化Delta V再现与周期时间有关的LV压力响应Delta P(t)的能力。所有的Delta P(t)都由三个阶段组成:阶段1,与Delta V的前沿同时发生;阶段1,与Delta V的上升沿同时发生;以及周期3的变化。阶段2,从阶段1短暂恢复;和阶段3,持续到收缩期。每个阶段都随着周期中Delta P(t)的变化而变化。当模型适合数据时,与单独使用Ca2 +激活相比,需要协同激活来维持收缩期更长。该模型成功地再现了测得的Delta P(t)响应的所有主要特征,因此可作为潜在收缩过程在LV功能中作用的可靠指标。

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