Rezakhaniha Rana, Stergiopulos Nikos
Hemodynamics and Cardiovascular Technology Laboratory (LHTC), School of Life Sciences, Institute of Bioengineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
J Biomech Eng. 2008 Jun;130(3):031017. doi: 10.1115/1.2907749.
The three-dimensional biomechanical behavior of the vascular wall is best described by means of strain energy functions. Significant effort has been devoted lately in the development of structure-based models of the vascular wall, which account for the individual contribution of each major structural component (elastin, collagen, and vascular smooth muscle). However, none of the currently proposed structural models succeeded in simultaneously and accurately describing both the pressure-radius and pressure-longitudinal force curves. We have hypothesized that shortcomings of the current models are, in part, due to unaccounted anisotropic properties of elastin. We extended our previously developed biomechanical model to account for elastin anisotropy. The experimental data were obtained from inflation-extension tests on facial veins of five young white New Zealand rabbits. Tests have been carried out under a fully relaxed state of smooth muscle cells for longitudinal stretch ratios ranging from 100% to 130% of the in vivo length. The experimental data (pressure-radius, pressure-force, and zero-stress-state geometries) provided a complete biaxial mechanical characterization of rabbit facial vein and served as the basis for validating the applicability and accuracy of the new biomechanical model of the venous wall. When only the pressure-radius curves were fitted, both the anisotropic and the isotropic models gave excellent results. However, when both pressure-radius and pressure-force curves are simultaneously fitted, the model with isotropic elastin shows an average weighted residual sum of squares of 8.94 and 23.9 in the outer radius and axial force, respectively, as compared to averages of 6.07 and 4.00, when anisotropic elastin is considered. Both the Alkaike information criterion and Schwartz criterion show that the model with the anisotropic elastin is more successful in predicting the data for a wide range of longitudinal stretch ratios. We conclude that anisotropic description of elastin is required for a full 3D characterization of the biomechanics of the venous wall.
血管壁的三维生物力学行为最好通过应变能函数来描述。最近,人们在开发基于结构的血管壁模型方面投入了大量精力,这些模型考虑了每个主要结构成分(弹性蛋白、胶原蛋白和血管平滑肌)的单独贡献。然而,目前提出的结构模型中没有一个能够同时准确地描述压力-半径和压力-纵向力曲线。我们推测,当前模型的缺点部分是由于弹性蛋白未被考虑的各向异性特性。我们扩展了我们之前开发的生物力学模型,以考虑弹性蛋白的各向异性。实验数据来自对五只年轻的白色新西兰兔面部静脉进行的充气-拉伸试验。试验是在平滑肌细胞完全松弛的状态下进行的,纵向拉伸比范围为体内长度的100%至130%。实验数据(压力-半径、压力-力和零应力状态几何形状)提供了兔面部静脉完整的双轴力学特征,并作为验证静脉壁新生物力学模型适用性和准确性的基础。当仅拟合压力-半径曲线时,各向异性模型和各向同性模型都给出了出色的结果。然而,当同时拟合压力-半径和压力-力曲线时,与考虑各向异性弹性蛋白时的平均值6.07和4.00相比,具有各向同性弹性蛋白的模型在外半径和轴向力方面的平均加权残差平方和分别为8.94和23.9。赤池信息准则和施瓦茨准则均表明,具有各向异性弹性蛋白的模型在预测广泛纵向拉伸比的数据方面更成功。我们得出结论,为了对静脉壁生物力学进行完整的三维表征,需要对弹性蛋白进行各向异性描述。