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A theoretical and non-destructive experimental approach for direct inclusion of measured collagen orientation and recruitment into mechanical models of the artery wall

机译:一种理论和非破坏性的实验方法,可直接将测得的胶原蛋白取向和募集纳入动脉壁的力学模型

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Gradual collagen recruitment has been hypothesized as the underlying mechanism for the mechanical stiffening with increasing stress in arteries. In this work, we investigated this hypothesis in eight rabbit carotid arteries by directly measuring the distribution of collagen recruitment stretch under increasing circumferential loading using a custom uniaxial (UA) extension device combined with a multi-photon microscope (MPM). This approach allowed simultaneous mechanical testing and imaging of collagen fibers without traditional destructive fixation methods. Fiber recruitment was quantified from 3D rendered MPM images, and fiber orientation was measured in projected stacks of images. Collagen recruitment was observed to initiate at a finite strain, corresponding to a sharp increase in the measured mechanical stiffness, confirming the previous hypothesis and motivating the development of a new constitutive model to capture this response.Previous constitutive equations for the arterial wall have modeled the collagen contribution with either abrupt recruitment at zero strain, abrupt recruitment at finite strain or as gradual recruitment beginning at infinitesimal strain. Based on our experimental data, a new combined constitutive model was presented in which fiber recruitment begins at a finite strain with activation stretch represented by a probability distribution function. By directly including this recruitment data, the collagen contribution was modeled using a simple Neo-Hookean equation. As a result, only two phenomenological material constants were required from the fit to the stress stretch data. Three other models for the arterial wall were then compared with these results. The approach taken here was successful in combining stress-strain analysis with simultaneous microstructural imaging of collagen recruitment and orientation, providing a new approach by which underlying fiber architecture may be quantified and included in constitutive equations.
机译:胶原逐渐补充被认为是随着动脉压力增加而机械僵硬的基本机制。在这项工作中,我们通过使用定制的单轴(UA)扩展装置结合多光子显微镜(MPM)直接测量在增加的周向负荷下胶原蛋白募集拉伸的分布,从而研究了八只兔颈动脉中的这一假设。这种方法可以同时进行胶原纤维的机械测试和成像,而无需传统的破坏性固定方法。从3D渲染的MPM图像中量化纤维的募集,并在投影的图像堆栈中测量纤维的方向。观察到胶原蛋白募集在有限的应变下开始,这与所测得的机械刚度的急剧增加相对应,从而证实了先前的假设并激励了新的本构模型的发展以捕获这种反应。以前的动脉壁本构方程已将其建模为在零应变时突然募集,在有限应变时突然募集或从无穷小应变开始逐渐募集的胶原蛋白贡献。根据我们的实验数据,提出了一种新的组合本构模型,其中纤维募集始于具有概率分布函数表示的激活拉伸的有限应变。通过直接包括该募集数据,使用简单的新霍克方程式对胶原蛋白贡献进行建模。结果,从拟合到应力拉伸数据仅需要两个现象学的材料常数。然后将其他三个动脉壁模型与这些结果进行了比较。此处采用的方法成功地将应力应变分析与胶原蛋白募集和定向的同时显微结构成像相结合,提供了一种新的方法,通过该方法可以量化基础纤维结构并将其包括在本构方程中。

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