Arteries exhibit a remarkable ability to adapt to diverse genetic defects and sustained alterations in mechanical loading. For example, changes in blood flow induced wall shear stress tend to control arterial caliber and changes in blood pressure induced circumferential wall stress tend to control wall thickness. We Submit, however, that the axial component of wall stress plays a similarly fundamental role in controlling arterial geometry, Structure, and function, that is, compensatory adaptations. This observation comes from a review of findings reported in the literature and a comparison Of four recent Studies from Our laboratory that quantified changes in the biaxial mechanical Properties of mouse carotid arteries in cases of altered cell-matrix interactions, extracellular matrix composition, blood pressure, or axial extension. There is, therefore, a pressing need to include the fundamental role of axial wall Stress in conceptual and theoretical models of arterial growth and remodeling and, consequently, there is a need for increased attention to evolving biaxial mechanical properties in cases of altered genetics and mechanical stimuli. (C) 2008 Elsevier Ltd. All rights reserved.
Fundamental role of axial stress in compensatory adaptations by arteries
Creators
J. D. Humphrey - Texas A&M University
J. F. Eberth - Texas A&M University
W. W. Dye - Texas A&M University
R. L. Gleason - The Wallace H. Coulter Department of Biomedical Engineering
Publication Details
Journal of biomechanics, v 42(1), pp 1-8
Publisher
Elsevier
Number of pages
8
Grant note
R01HL080415 / NATIONAL HEART, LUNG, AND BLOOD INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI)
R01EB008366 / NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Biomedical Imaging & Bioengineering (NIBIB)
HL-64372; HL-80415; HL-86418; EB-08366 / NIH; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA
Resource Type
Journal article
Language
English
Academic Unit
School of Biomedical Engineering, Science, and Health Systems
Web of Science ID
WOS:000263191300001
Scopus ID
2-s2.0-58149468382
Other Identifier
991021902502104721
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Collaboration types
Domestic collaboration
Web of Science research areas
Biophysics
Engineering, Biomedical
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