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Differential mechanical response and microstructural organization between non-human primate femoral and carotid arteries
Authors:Ruoya Wang  Julia Raykin  Haiyan Li  Rudolph L Gleason Jr  Luke P Brewster
Institution:1. George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA
2. Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, USA
3. Division of Vascular Surgery, Department of Surgery, Emory University School of Medicine, Atlanta, GA, USA
4. Parker H. Petit Institute of Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA, USA
5. Atlanta VA Medical Center, Surgical and Research Services, 101 Woodruff Circle, 5211 WMB, Atlanta, GA?, 30322?, USA
Abstract:Unique anatomic locations and physiologic functions predispose different arteries to varying mechanical responses and pathologies. However, the underlying causes of these mechanical differences are not well understood. The objective of this study was to first identify structural differences in the arterial matrix that would account for the mechanical differences between healthy femoral and carotid arteries and second to utilize these structural observations to perform a microstructurally motivated constitutive analysis. Femoral and carotid arteries were subjected to cylindrical biaxial loading and their microstructure was quantified using two-photon microscopy. The femoral arteries were found to be less compliant than the carotid arteries at physiologic loads, consistent with previous studies, despite similar extracellular compositions of collagen and elastin ( \(P> 0.05\) ). The femoral arteries exhibited significantly less circumferential dispersion of collagen fibers ( \(P< 0.05\) ), despite a similar mean fiber alignment direction as the carotid arteries. Elastin transmural distribution, in vivo axial stretch, and opening angles were also found to be distinctly different between the arteries. Lastly, we modeled the arteries’ mechanical behaviors using a microstructural-based, distributed collagen fiber constitutive model. With this approach, the material parameters of the model were solved using the experimental microstructural observations. The findings of this study support an important role for microstructural organization in arterial stiffness.
Keywords:
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