Cs. Lee et Jm. Tarbell, INFLUENCE OF VASOACTIVE DRUGS ON WALL SHEAR-STRESS DISTRIBUTION IN THE ABDOMINAL AORTIC BIFURCATION - AN IN-VITRO STUDY, Annals of biomedical engineering, 26(2), 1998, pp. 200-212
The present study compares the wall shear stress (rate) distribution i
n a compliant aortic bifurcation model under three different hemodynam
ic states: normal state, angiotensin II infusion state (vasoconstricto
r), and isoproterenol infusion state (vasodilator). Using a Newtonian
blood analog fluid, flow wave forms corresponding to each flow state w
ere generated in an in vitro flow loop and a photographic flow visuali
zation technique was employed to measure wall shear rate. The results
indicate a zone of low mean wall shear stress and highly oscillatory s
hear stress on the outer (lateral) wall of the bifurcation. In this zo
ne, the mean wall shear stress became negative for all three hemodynam
ic states indicating flow separation. However, the spatial extent of t
he flow separation zone was not affected significantly by the flow sta
te. The study also revealed a large spatial variation of the phase ang
le between the hoop strain (circumferential strain due to radial arter
y expansion) and the wall shear stress, the two main mechanical stimul
i acting on endothelial cells which affect their biology. In the zone
of low mean wall shear stress on the outer wall, the two stimuli were
more out of phase relative to the mother branch, whereas they were les
s out of phase (by about 50 degrees) on the inner wall (flow divider s
ide). This phase angle was affected significantly by the flow state. F
or angiotensin II, the phase angle reached a maximum of 125 degrees in
the low mean shear zone while the maximum was 94 degrees and 66 degre
es for the normal and isoproterenol states, respectively. Our observat
ion that large phase angles between the hoop strain and wall shear str
ess wave forms are localized in the low shear stress region where athe
rosclerotic disease occurs suggests the possible physiological relevan
ce of this phase angle to the development of atherosclerosis. (C) 1998
Biomedical Engineering Society.