Tissue and microstructural deformations in aortic tissue under stretch and after deformation recovery

Elucidating how cardiovascular biomechanics is regulated during health and disease is critical for developing diagnostic and therapeutic methods. The extracellular matrix of cardiovascular tissue is composed of multiple fibrillar networks embedded in an amorphous ground substance and has been found to reveal time-dependent mechanical behavior. Given the multiscale nature of tissue biomechanics, an accurate description of cardiovascular biomechanics can be obtained only when microstructural morphology is characterized and put together in correlation with tissue-scale mechanics. In this study, we sought to determine how the microstructural configuration in aortic tissue changes with tissue-scale loading protocols. At the tissue level, rather intuitively, the width and thickness decrease when specimens undergo elongation and it is found that there is a higher inverse correlation between the elongation of circumferential specimens and the shrinkage along the thickness than along the width. After deformation recovery, the specimens show levels of permanent deformation in both thickness and width as neither recovers the initial values for the unstretched specimen, with higher permanent deformation measured for thickness. At the microstructural level, the networks in the wall inner layer show straighter fibrillar structure under stretch, which partly returns to the crimping structure after deformation recovery. This study indicates a microstructural basis for observations of regional permanent tissue stretch in artery tissues, and furnishes early data for developing multiscale models of cardiovascular viscoelastic/viscoplastic modeling.

[1]  K. Ishak,et al.  Histological grading and staging of chronic hepatitis. , 1995 .

[2]  M. R. Roach,et al.  The composition and mechanical properties of abdominal aortic aneurysms. , 1994, Journal of vascular surgery.

[3]  C. Lacabanne,et al.  Characterisation of elastin and collagen in aortic bioprostheses , 2000, Medical and Biological Engineering and Computing.

[4]  Radek Holota,et al.  Microscopic image analysis of elastin network in samples of normal, atherosclerotic and aneurysmatic abdominal aorta and its biomechanical implications , 2003 .

[5]  J D Humphrey,et al.  Denaturation of collagen via heating: an irreversible rate process. , 2002, Annual review of biomedical engineering.

[6]  D. Bergel,et al.  The visco-elastic properties of the arterial wall. , 1960 .

[7]  E. Brunt,et al.  Grading and staging the histopathological lesions of chronic hepatitis: The Knodell histology activity index and beyond , 2000, Hepatology.

[8]  J D Humphrey,et al.  An evaluation of pseudoelastic descriptors used in arterial mechanics. , 1999, Journal of biomechanical engineering.

[9]  Julia T. Apter,et al.  Correlation of Visco‐elastic Properties of Large Arteries with Microscopic Structure , 1966, Circulation research.

[10]  R. N. Vaishnav,et al.  Residual stress and strain in aortic segments. , 1987, Journal of biomechanics.

[11]  C. P. Winlove,et al.  The distribution of water in arterial elastin: Effects of mechanical stress, osmotic pressure, and temperature , 1995, Biopolymers.

[12]  Danial Shahmirzadi,et al.  Tissue- and Microstructural-level Deformation of Aortic Tissue under Viscoelastic/Viscoplastic Loading , 2011 .

[13]  Julia T. Apter,et al.  Correlation of Visco‐Elastic Properties with Microscopic Structure of Large Arteries: IV. THERMAL RESPONSES OF COLLAGEN, ELASTIN, SMOOTH MUSCLE, AND INTACT ARTESRIES , 1967, Circulation research.

[14]  Karen Cherubini,et al.  Comparison between semi-automated segmentation and manual point-counting methods for quantitative analysis of histological sections. , 2006, Journal of oral science.

[15]  R. Bolender Biological stereology: History, present state, future directions , 1992, Microscopy research and technique.

[16]  D. Hopwood Some aspects of fixation with glutaraldehyde. A biochemical and histochemical comparison of the effects of formaldehyde and glutaraldehyde fixation on various enzymes and glycogen, with a note on penetration of glutaraldehyde into liver. , 1967, Journal of anatomy.

[17]  P. Flory,et al.  The Elastic Properties of Elastin1,2 , 1958 .

[18]  J. Gosline,et al.  Elastin dehydration through the liquid and the vapor phase: a comparison of osmotic stress models. , 1998, Biopolymers.

[19]  J. Brzezinski,et al.  Dielectric relaxation of a protein–water system in atherosclerotic artery wall , 2007, Medical & Biological Engineering & Computing.

[20]  Gamal M Dahab,et al.  Digital quantification of fibrosis in liver biopsy sections: Description of a new method by Photoshop software , 2004, Journal of gastroenterology and hepatology.

[21]  Neil Kaplowitz,et al.  Formulation and application of a numerical scoring system for assessing histological activity in asymptomatic chronic active hepatitis , 1981, Hepatology.

[22]  M J Puddephat,et al.  The benefit of stereology for quantitative radiology. , 2000, The British journal of radiology.

[23]  Danial Shahmirzadi,et al.  Effects of Arterial Tissue Storage and Burst Failure on Residual Stress Relaxation , 2012 .

[24]  A. Avolio,et al.  Quantification of alterations in structure and function of elastin in the arterial media. , 1998, Hypertension.

[25]  anxin Sun,et al.  Nonlinear optical microscopy : use of second harmonic generation and two-photon microscopy for automated quantitative liver fibrosis studies , 2008 .

[26]  E R Weibel,et al.  Measuring through the microscope: Development and evolution of stereological methods , 1989, Journal of microscopy.

[27]  Mp Mirjam Rubbens,et al.  Quantification of collagen orientation in 3D engineered tissue , 2007 .

[28]  D. C. Sheehan,et al.  Theory and Practice of Histotechnology , 1980 .

[29]  M Scandola,et al.  The low‐temperature mechanical relaxation of elastin. I. The dry protein , 1976, Biopolymers.

[30]  M. Kojiro,et al.  Long‐term evolution of fibrosis from chronic hepatitis to cirrhosis in patients with hepatitis C: Morphometric analysis of repeated biopsies , 1997, Hepatology.

[31]  Y. Fung,et al.  Biomechanics: Mechanical Properties of Living Tissues , 1981 .

[32]  J. Gosline,et al.  The effects of heating on the mechanical properties of arterial elastin. , 1994, Connective tissue research.

[33]  P J Flory,et al.  The elastic properties of elastin , 1974, Biopolymers.

[34]  Anita Driessen-Mol,et al.  Quantification of the Temporal Evolution of Collagen Orientation in Mechanically Conditioned Engineered Cardiovascular Tissues , 2009, Annals of Biomedical Engineering.

[35]  Eli J Weinberg,et al.  On the multiscale modeling of heart valve biomechanics in health and disease , 2010, Biomechanics and modeling in mechanobiology.

[36]  Winsome Garvey,et al.  A Modified Verhoeff Elastic-van Gieson Stain , 1991 .

[37]  Valeer J Desmet,et al.  Knodell RG, Ishak KG, Black WC, Chen TS, Craig R, Kaplowitz N, Kiernan TW, Wollman J. Formulation and application of a numerical scoring system for assessing histological activity in asymptomatic chronic active hepatitis [Hepatology 1981;1:431-435]. , 2003, Journal of hepatology.

[38]  M. Lindgren,et al.  Quantification of the second-order nonlinear susceptibility of collagen I using a laser scanning microscope. , 2007, Journal of biomedical optics.

[39]  O. James Drugs and the ageing liver. , 1985, Journal of hepatology.