Finite Element Simulation of Opening Angle Response of Porcine Aortas Using Layer Specific GAG Distributions in One and Two Layered Solid Matrices.

IF 1.6 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Engineering and Technology Pub Date : 2024-10-02 DOI:10.1007/s13239-024-00754-x
Noor M Ghadie, Jean-Philippe St-Pierre, Michel R Labrosse
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Abstract

Purpose: Recent studies have identified an effect of glycosaminoglycans (GAG) on residual stresses in the aorta, underscoring the need to better understand their biomechanical roles.

Methods: Aortic ring models for each of the ascending, arch and descending thoracic regions of the porcine thoracic aorta were created in FEBioStudio, using a framework that incorporates the Donnan osmotic swelling in a porous solid matrix. The distribution of fixed charge densities (FCD) through the thickness of the tissue was prescribed as calculated from experimentally quantified sulfated GAG mural distributions. Material parameters for the solid matrix, modeled using a Holmes-Mow constitutive law, were optimized using data from biaxial tensile tests. In addition to modelling the solid matrix as one layer, two layers were considered to capture the differences between the intima-media and the adventitia, for which various stiffness ratios were explored.

Results: As the stiffness of the adventitia with respect to that of the media increased, the simulated opening angle increased. The opening angle also decreased from the ascending to the descending thoracic region in both one- and two-layered solid matrices models. The simulated results were compared against the experimental contribution of GAG to the opening angle, as previously quantified via enzymatic GAG-depletion. When using one layer for the solid matrix, the errors between the simulated opening angles and the experimental contribution of GAG to the opening angle were respectively 28%, 15% and 23% in the ascending, arch and descending thoracic regions. When using two layers for the solid matrix, the smallest errors in the ascending and arch regions were 21% and 5% when the intima-media was modelled as 10 times stiffer, and as twice stiffer than the adventitia, respectively, and 23% in the descending thoracic regions when the intima-media and adventitia shared similar mechanical properties.

Conclusions: Overall, this study demonstrates that GAG partially contribute to circumferential residual stress, and that GAG swelling is one of several regulators of the opening angle. The minor discrepancies between simulated and experimental opening angles imply that the contribution of GAG extends beyond mere swelling, aligning with previous experimental indications of their interaction with ECM fibers in determining the opening angle.

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利用单层和双层固体基质中特定层的 GAG 分布对猪主动脉开口角响应的有限元模拟
目的:最近的研究发现了糖胺聚糖(GAG)对主动脉残余应力的影响:最近的研究发现了糖胺聚糖(GAG)对主动脉残余应力的影响,强调了更好地了解其生物力学作用的必要性:方法:在 FEBioStudio 中创建了猪胸主动脉的升主动脉环、弓主动脉环和降主动脉环模型,使用的框架结合了多孔固体基质中的唐南渗透膨胀。固定电荷密度 (FCD) 在组织厚度上的分布是根据实验量化的硫酸化 GAG 壁层分布计算得出的。固体基质的材料参数采用霍姆斯-莫氏构成定律建模,并利用双轴拉伸试验的数据进行了优化。除了将固体基质建模为一层外,还考虑了两层,以捕捉内中膜和外膜之间的差异,并探讨了各种刚度比:结果:随着临膜相对于介质的刚度增加,模拟的开口角也随之增加。在单层和双层实心基质模型中,从胸腔升部到降部的开口角度也有所减小。模拟结果与实验中 GAG 对打开角度的贡献进行了比较,实验中的 GAG 是通过酶解 GAG 来量化的。当使用单层固体基质时,在胸腔升部、弓部和降部,模拟打开角度与实验中 GAG 对打开角度的贡献之间的误差分别为 28%、15% 和 23%。当使用两层固体基质时,在升胸区和弓区,当内膜中层被模拟为比外膜中层坚硬 10 倍和两倍时,最小误差分别为 21% 和 5%,而在降胸区,当内膜中层和外膜中层具有相似的机械特性时,最小误差为 23%:总之,这项研究证明了 GAG 对周向残余应力的部分作用,以及 GAG 的膨胀是开角的几个调节因素之一。模拟开口角度与实验开口角度之间的微小差异意味着 GAG 的作用不仅限于膨胀,这与之前实验表明 GAG 与 ECM 纤维在决定开口角度方面的相互作用相一致。
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来源期刊
Cardiovascular Engineering and Technology
Cardiovascular Engineering and Technology Engineering-Biomedical Engineering
CiteScore
4.00
自引率
0.00%
发文量
51
期刊介绍: Cardiovascular Engineering and Technology is a journal publishing the spectrum of basic to translational research in all aspects of cardiovascular physiology and medical treatment. It is the forum for academic and industrial investigators to disseminate research that utilizes engineering principles and methods to advance fundamental knowledge and technological solutions related to the cardiovascular system. Manuscripts spanning from subcellular to systems level topics are invited, including but not limited to implantable medical devices, hemodynamics and tissue biomechanics, functional imaging, surgical devices, electrophysiology, tissue engineering and regenerative medicine, diagnostic instruments, transport and delivery of biologics, and sensors. In addition to manuscripts describing the original publication of research, manuscripts reviewing developments in these topics or their state-of-art are also invited.
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