Document Detail


Transitional flow at the venous anastomosis of an arteriovenous graft: potential activation of the ERK1/2 mechanotransduction pathway.
MedLine Citation:
PMID:  12661196     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We present experimental and computational results that describe the level, distribution, and importance of velocity fluctuations within the venous anastomosis of an arteriovenous graft. The motivation of this work is to understand better the importance of biomechanical forces in the development of intimal hyperplasia within these grafts. Steady-flow in vitro studies (Re = 1060 and 1820) were conducted within a graft model that represents the venous anastomosis to measure velocity by means of laser Doppler anemometry. Numerical simulations with the same geometry and flow conditions were conducted by employing the spectral element technique. As flow enters the vein from the graft, the velocity field exhibits flow separation and coherent structures (weak turbulence) that originate from the separation shear layer. We also report results of a porcine animal study in which the distribution and magnitude of vein-wall vibration on the venous anastomosis were measured at the time of graft construction. Preliminary molecular biology studies indicate elevated activity levels of the extracellular regulatory kinase ERK1/2, a mitogen-activated protein kinase involved in mechanotransduction, at regions of increased vein-wall vibration. These findings suggest a potential relationship between the associated turbulence-induced vein-wall vibration and the development of intimal hyperplasia in arteriovenous grafts. Further research is necessary, however, in order to determine if a correlation exists and to differentiate the vibration effect from that of flow related effects.
Authors:
Francis Loth; Paul F Fischer; Nurullah Arslan; Christopher D Bertram; Seung E Lee; Thomas J Royston; Wael E Shaalan; Hisham S Bassiouny
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Publication Detail:
Type:  Comparative Study; Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Validation Studies    
Journal Detail:
Title:  Journal of biomechanical engineering     Volume:  125     ISSN:  0148-0731     ISO Abbreviation:  J Biomech Eng     Publication Date:  2003 Feb 
Date Detail:
Created Date:  2003-03-28     Completed Date:  2003-09-26     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  7909584     Medline TA:  J Biomech Eng     Country:  United States    
Other Details:
Languages:  eng     Pagination:  49-61     Citation Subset:  IM    
Affiliation:
Department of Mechanical Engineering and Industrial Engineering, University of Illinois at Chicago, Chicago, Illinois 60607, USA. floth@uic.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Aorta / metabolism,  pathology,  physiopathology,  surgery
Arteriovenous Anastomosis / metabolism,  pathology,  physiopathology*
Blood Flow Velocity
Blood Vessel Prosthesis
Computer Simulation
Hemorheology / methods
Iliac Vein / metabolism,  pathology,  physiopathology*,  surgery
Mechanotransduction, Cellular
Mitogen-Activated Protein Kinase 1 / metabolism
Mitogen-Activated Protein Kinase 3
Mitogen-Activated Protein Kinases / metabolism*
Models, Cardiovascular*
Shear Strength
Stress, Mechanical
Swine
Tissue Distribution
Veins / metabolism,  pathology,  physiopathology,  surgery
Chemical
Reg. No./Substance:
EC 2.7.11.24/Mitogen-Activated Protein Kinase 1; EC 2.7.11.24/Mitogen-Activated Protein Kinase 3; EC 2.7.11.24/Mitogen-Activated Protein Kinases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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