Parameter Sensitivity Study of a Constrained Mixture Model of Arterial Growth and Remodeling
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Valentín, Complementary Vasoactivity and Matrix Remodelling in Arterial Adaptations to Altered Flow and Pressure, J. R. Soc., Interface, 6, 293, 10.1098/rsif.2008.0254
Baek, A Theoretical Model of Enlarging Intracranial Fusiform Aneurysms, ASME J. Biomech. Eng., 128, 142, 10.1115/1.2132374
Baek, Biochemomechanics of Cerebral Vasospasm and Its Resolution: II. Constitutive Relations and Model Simulations, Ann. Biomed. Eng., 35, 1498, 10.1007/s10439-007-9322-x
Baek, Competition Between Radial Expansion and Thickening in the Enlargement of an Intracranial Saccular Aneurysm, J. Elast., 80, 13, 10.1007/s10659-005-9004-6
Figueroa, C. A., Baek, S., Taylor, C. A., and Humphrey, J. D., 2009, “A Computational Framework for Fluid-Solid-Growth Modeling in Cardiovascular Simulations,” Comput. Methods Appl. Mech. Eng.0045-7825 (to be published).
Valentín, Evaluation of Fundamental Hypotheses Underlying Constrained Mixture Models of Arterial Growth and Remodeling, Philos. Trans. R. Soc. London, Ser. A, 367, 3585, 10.1098/rsta.2009.0113
Anderson, Verification, Validation and Sensitivity Studies in Computational Biomechanics, Comput. Methods Biomech. Biomed. Eng., 10, 171, 10.1080/10255840601160484
Lodi, Hemodynamic Effect of Cerebral Vasospasm in Humans: A Modeling Study, Ann. Biomed. Eng., 27, 257, 10.1114/1.168
Wicker, Normal Basilar Artery Structure and Biaxial Mechanical Behaviour, Comput. Methods Biomech. Biomed. Eng., 11, 539, 10.1080/10255840801949793
Fischer, Collagen and Elastin Content in Canine Arteries Selected From Functionally Different Vascular Beds, Circ. Res., 19, 394, 10.1161/01.RES.19.2.394
Walmsley, Interrelationships Among Wall Structure, Smooth Muscle Orientation, and Contraction in Human Major Cerebral Arteries, Stroke, 14, 781, 10.1161/01.STR.14.5.781
Holzapfel, A New Constitutive Framework for Arterial Wall Mechanics and a Comparative Study of Material Models, J. Elast., 61, 1, 10.1023/A:1010835316564
Cardamone, L., Valentín, A., Eberth, J. F., and Humphrey, J. D., 2009, “Origin of Axial Prestretch and Residual Stress in Arteries,” Biomech. Model. Mechanobiol.1617-7959 (to be published).
Lanir, Constitutive Equations for Fibrous Connective Tissues, J. Biomech., 16, 1, 10.1016/0021-9290(83)90041-6
Gleason, A 2-d Model of Flow-Induced Alterations in the Geometry, Structure, and Properties of Carotid Arteries, ASME J. Biomech. Eng., 126, 371, 10.1115/1.1762899
Price, Length-Dependent Sensitivity in Vascular Smooth Muscle, Am. J. Physiol., 241, H557
Rachev, Theoretical Study of the Effects of Vascular Smooth Muscle Contraction on Strain and Stress Distributions in Arteries, Ann. Biomed. Eng., 27, 459, 10.1114/1.191
Zamir, Shear Forces and Blood Vessel Radii in the Cardiovascular System, J. Gen. Physiol., 69, 449, 10.1085/jgp.69.4.449
Murray, The Physiological Principle of Minimum Work: I. the Vascular System and the Cost of Blood Volume, Proc. Natl. Acad. Sci. U.S.A., 12, 207, 10.1073/pnas.12.3.207
Stenmark, Cellular and Molecular Mechanisms of Pulmonary Vascular Remodeling, Annu. Rev. Physiol., 59, 89, 10.1146/annurev.physiol.59.1.89
Leung, Cyclic Stretching Stimulates Synthesis of Matrix Components by Arterial Smooth Muscle Cells In Vitro, Science, 191, 475, 10.1126/science.128820
Wilson, Mechanical Strain Induces Growth of Vascular Smooth Muscle Cells Via Autocrine Action of PDGF, J. Cell Biol., 123, 741, 10.1083/jcb.123.3.741
Li, Stretch-Induced Collagen Synthesis in Cultured Smooth Muscle Cells From Rabbit Aortic Media and a Possible Involvement of Angiotensin II and Transforming Growth Factor-β, J. Vasc. Res., 35, 93, 10.1159/000025570
O’Callaghan, Mechanical Strain-Induced Extracellular Matrix Production by Human Vascular Smooth Muscle Cells: Role of TGF-β1, Hypertension, 36, 319, 10.1161/01.HYP.36.3.319
Sluijter, Increase in Collagen Turnover but Not in Collagen Fiber Content Is Associated With Flow-Induced Arterial Remodeling, J. Vasc. Res., 41, 546, 10.1159/000081972
Mondy, Platelet-Derived Growth Factor Ligand and Receptor Expression in Response to Altered Blood Flow In Vivo, Circ. Res., 81, 320, 10.1161/01.RES.81.3.320
Cho, Effects of Changes in Blood Flow Rate on Cell Death and Cell Proliferation in Carotid Arteries of Immature Rabbits, Circ. Res., 81, 328, 10.1161/01.RES.81.3.328
Xu, Molecular Mechanisms of Aortic Wall Remodeling in Response to Hypertension, J. Vasc. Surg., 33, 570, 10.1067/mva.2001.112231
Nissen, Increased Turnover of Arterial Collagen in Hypertensive Rats, Proc. Natl. Acad. Sci. U.S.A., 75, 451, 10.1073/pnas.75.1.451
Jamal, Structural Changes and Recovery of Function After Arterial Injury, Arterioscler. Thromb., 12, 307, 10.1161/01.ATV.12.3.307
Xu, Differential Transmural Distribution of Gene Expression for Collagen Types I and III Proximal to Aortic Coarctation in the Rabbit, J. Vasc. Res., 37, 170, 10.1159/000025728
Humphrey, Fundamental Role of Axial Stress in Compensatory Adaptations by Arteries, J. Biomech., 42, 1, 10.1016/j.jbiomech.2008.11.011
Jackson, Wall Tissue Remodeling Regulates Longitudinal Tension in Arteries, Circ. Res., 90, 918, 10.1161/01.RES.0000016481.87703.CC
Sluijter, Increased Collagen Turnover Is Only Partly Associated With Collagen Fiber Deposition in the Arterial Response to Injury, Cardiovasc. Res., 61, 186, 10.1016/j.cardiores.2003.09.028
Strauss, In Vivo Collagen Turnover Following Experimental Balloon Angioplasty Injury and the Role of Matrix Metalloproteinases, Circ. Res., 79, 541, 10.1161/01.RES.79.3.541
Strauss, Extracellular Matrix Remodeling After Balloon Angioplasty Injury in a Rabbit Model of Restenosis, Circ. Res., 75, 650, 10.1161/01.RES.75.4.650
Karim, Histomorphometric and Biochemical Correlates of Arterial Procollagen Gene Expression During Vascular Repair After Experimental Angioplasty, Circulation, 91, 2049, 10.1161/01.CIR.91.7.2049
Bendeck, Smooth Muscle Cell Matrix Metalloproteinase Production is Stimulated Via αvβ3 Integrin, Arterioscler., Thromb., Vasc. Biol., 20, 1467, 10.1161/01.ATV.20.6.1467
Weiser-Evans, Transient Reexpression of an Embryonic Autonomous Growth Phenotype by Adult Carotid Artery Smooth Muscle Cells After Vascular Injury, J. Cell Physiol., 182, 12, 10.1002/(SICI)1097-4652(200001)182:1<12::AID-JCP2>3.0.CO;2-G
Shi, Adventitial Remodeling After Coronary Arterial Injury, Circulation, 93, 340, 10.1161/01.CIR.93.2.340
Thakker-Varia, Expression of Matrix-Degrading Enzymes in Pulmonary Vascular Remodeling in the Rat, Am. J. Physiol., 275, L398
Rizvi, The Effects of Endothelin-1 on Collagen Type I and Type III Synthesis in Cultured Porcine Coronary Artery Vascular Smooth Muscle Cells, J. Mol. Cell. Cardiol., 28, 243, 10.1006/jmcc.1996.0023
Rizvi, Nitric Oxide Modulates Basal and Endothelin-Induced Coronary Artery Vascular Smooth Muscle Cell Proliferation and Collagen Levels, J. Mol. Cell. Cardiol., 29, 1779, 10.1006/jmcc.1996.0480
Dooley, Effect of Nitric Oxide and Peroxynitrite on Type I Collagen Synthesis in Normal and Scleroderma Dermal Fibroblasts, Free Radic Biol. Med., 43, 253, 10.1016/j.freeradbiomed.2007.04.017
Uematsu, Regulation of Endothelial Cell Nitric Oxide Synthase mRNA Expression by Shear Stress, Am. J. Physiol., 269, C1371, 10.1152/ajpcell.1995.269.6.C1371
Malek, Physiological Fluid Shear Stress Causes Downregulation of Endothelin-1 mRNA in Bovine Aortic Endothelium, Am. J. Physiol., 263, C389, 10.1152/ajpcell.1992.263.2.C389
Singh, Basic Fibroblast Growth Factor Expression Precedes Flow-Induced Arterial Enlargement, J. Surg. Res., 77, 165, 10.1006/jsre.1998.5376
Taber, A Model for Aortic Growth Based on Fluid Shear and Fiber Stresses, ASME J. Biomech. Eng., 120, 348, 10.1115/1.2798001
Rachev, A Model of Arterial Adaptation to Alterations in Blood Flow, J. Elast., 61, 83, 10.1023/A:1010800703478
Rodriguez-Vita, Endothelin-1, Via ETA Receptor and Independently of Transforming Growth Factor-β, Increases the Connective Tissue Growth Factor in Vascular Smooth Muscle Cells, Circ. Res., 97, 125, 10.1161/01.RES.0000174614.74469.83
Niedermüller, Investigations on the Kinetics of Collagen-Metabolism in Young and Old Rats, Exp. Gerontol., 12, 159, 10.1016/0531-5565(77)90001-8
Cho, Apoptosis (Programmed Cell Death) in Arteries of the Neonatal Lamb, Circ. Res., 76, 168, 10.1161/01.RES.76.2.168
Gelman, Collagen Fibril Formation. Evidence for a Multistep Process, J. Biol. Chem., 254, 180, 10.1016/S0021-9258(17)30289-2
Gelman, Collagen Fibril Formation In Vitro. The Role of the Nonhelical Terminal Regions, J. Biol. Chem., 254, 11741, 10.1016/S0021-9258(19)86545-6
Kao, Kinetics for the Secretion of Procollagen by Freshly Isolated Tendon Cells, J. Biol. Chem., 252, 8391, 10.1016/S0021-9258(19)75231-4
Jackson, Partial Off-Loading of Longitudinal Tension Induces Arterial Tortuosity, Arterioscler., Thromb., Vasc. Biol., 25, 957, 10.1161/01.ATV.0000161277.46464.11
Ellsmere, Mechanical Loading of Bovine Pericardium Accelerates Enzymatic Degradation, Biomaterials, 20, 1143, 10.1016/S0142-9612(99)00013-7
Ruberti, Strain-Controlled Enzymatic Cleavage of Collagen in Loaded Matrix, Biochem. Biophys. Res. Commun., 336, 483, 10.1016/j.bbrc.2005.08.128
Langille, Remodeling of Developing and Mature Arteries: Endothelium, Smooth Muscle, and Matrix, J. Cardiovasc. Pharmacol., 21, S11, 10.1097/00005344-199301000-00003
Langille, Arterial Remodeling: Relation to Hemodynamics, Can. J. Physiol. Pharmacol., 74, 834, 10.1139/cjpp-74-7-834
Humphrey, A Constrained Mixture Model for Growth and Remodeling of Soft Tissues, Math. Models Meth. Appl. Sci., 12, 407, 10.1142/S0218202502001714
Alberts, The Molecular Biology of the Cell, 4th ed.
Kelleher, Vascular Extracellular Matrix and Aortic Development, Curr. Top Dev. Biol., 62, 153, 10.1016/S0070-2153(04)62006-0
Meshel, Basic Mechanism of Three-Dimensional Collagen Fibre Transport by Fibroblasts, Nat. Cell Biol., 7, 157, 10.1038/ncb1216
Kozel, Elastic Fiber Formation: A Dynamic View of Extracellular Matrix Assembly Using Timer Reporters, J. Cell Physiol., 207, 87, 10.1002/jcp.20546
Hu, Stress-Strain Behavior of the Passive Basilar Artery in Normotension and Hypertension, J. Biomech., 40, 2559, 10.1016/j.jbiomech.2006.11.007
Truesdell, The Non-Linear Field Theories of Mechanics
Furchgott, The Obligatory Role of Endothelial Cells in the Relaxation of Arterial Smooth Muscle by Acetylcholine, Nature (London), 288, 373, 10.1038/288373a0
Pohl, Crucial Role of Endothelium in the Vasodilator Response to Increased Flow In Vivo, Hypertension, 8, 37, 10.1161/01.HYP.8.1.37
Dajnowiec, Arterial Adaptations to Chronic Changes in Haemodynamic Function: Coupling Vasomotor Tone to Structural Remodelling, Clin. Sci., 113, 15, 10.1042/CS20060337
Zarins, Shear Stress Regulation of Artery Lumen Diameter in Experimental Atherogenesis, J. Vasc. Surg., 5, 413, 10.1067/mva.1987.avs0050413
Lehman, Mechanism of Enlargement of Major Cerebral Collateral Arteries in Rabbits, Stroke, 22, 499, 10.1161/01.STR.22.4.499
Stålhand, Aorta In Vivo Parameter Identification Using an Axial Force Constraint, Biomech. Model. Mechanobiol., 3, 191, 10.1007/s10237-004-0057-4
Masson, Characterization of Arterial Wall Mechanical Behavior and Stresses From Human Clinical Data, J. Biomech., 41, 2618, 10.1016/j.jbiomech.2008.06.022
Nevo, Structural Finite Deformation Model of the Left Ventricle During Diastole and Systole, J. Biomech., 111, 342, 10.1115/1.3168389