The objective of this research is to gain a better understanding of the dynamic role played by stress and strain on the remodeling and growth of the blood vessels. When blood pressure or flow is increased above the normal, changes occur in the blood vessel lumen, wall thickness, zero- stress state, fine structure of the intima, media and adventitia layers, geometry and dimensions of the endothelial and smooth muscle cells, the mechanical properties of the intima-media and adventitial layers, capillaries, and even branching patterns and total generation numbers. Hence our HYPOTHESIS: Stress and strain are important factors that determine blood vessel structure and function, together with chemical factors. We want to document their influence mathematically, with the following SPECIFIC AIMS: 1) To determine the effects of changing blood shear and blood pressure on the remodeling of the blood vessels and express them in the form of indicial functions. 2) To obtain data on the morphology, histology and experimental mechanics of vessels and use them to calculate the stress and strain distribution and determine the strain energy functions of the intima-media and adventitia layers which change in the remodeling process. 3) To demonstrate the applications of the results by solving some key problems of the heart. The biology of growth and remodeling should be studied at all levels from atoms to the whole animal. The scale of the level chosen for the present study is that of the tissue with a minimum dimension in the mu-m range. In this length scale, our RATIONALE is that the engineering approach is the most efficient, in which questions in physiology and medicine can be converted to boundary - value problems whose solutions can be tested experimentally. In the process, we correct a current deficiency in biomedical science: people really do not know how to compute stress and strain in the tissues of blood vessels. We will make an effort to give biomechanics a firm foundation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL043026-08
Application #
6242072
Study Section
Project Start
1997-09-01
Project End
1998-08-31
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
8
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Dewan, Sukriti; McCabe, Kimberly J; Regnier, Michael et al. (2016) Molecular Effects of cTnC DCM Mutations on Calcium Sensitivity and Myofilament Activation-An Integrated Multiscale Modeling Study. J Phys Chem B 120:8264-75
Yao, Weijuan; Chu, Xin; Sung, Lanping Amy (2015) Cell type-restricted expression of erythrocyte tropomodulin Isoform41 in exon 1 knockout/LacZ knock-in heterozygous mice. Gene Expr Patterns 17:45-55
Sche, Paul; Vera, Carlos; Sung, L Amy (2011) Intertwined ** spectrin meeting helical actin protofilament in the erythrocyte membrane skeleton: wrap-around vs. point-attachment. Ann Biomed Eng 39:1984-93
de Oliveira, Mauricio; Vera, Carlos; Valdez, Pierre et al. (2010) Nanomechanics of multiple units in the erythrocyte membrane skeletal network. Ann Biomed Eng 38:2956-67
Yao, Weijuan; Sung, Lanping Amy (2010) Erythrocyte tropomodulin isoforms with and without the N-terminal actin-binding domain. J Biol Chem 285:31408-17
Su, Susan S; Schmid-Schönbein, Geert W (2010) Internalization of Formyl Peptide Receptor in Leukocytes Subject to Fluid Stresses. Cell Mol Bioeng 3:20-29
Yao, Weijuan; Sung, Lanping Amy (2009) Specific expression of E-Tmod (Tmod1) in horizontal cells: implications in neuronal cell mechanics and glaucomatous retina. Mol Cell Biomech 6:71-82
Schmid-Schönbein, Geert W (2009) 2008 Landis Award lecture. Inflammation and the autodigestion hypothesis. Microcirculation 16:289-306
Chien, Shu (2008) Effects of disturbed flow on endothelial cells. Ann Biomed Eng 36:554-62
Jacot, Jeffrey G; McCulloch, Andrew D; Omens, Jeffrey H (2008) Substrate stiffness affects the functional maturation of neonatal rat ventricular myocytes. Biophys J 95:3479-87

Showing the most recent 10 out of 205 publications