Effect of non-Newtonian and pulsatile blood flow on mass transport in the human aorta

J Biomech. 2011 Apr 7;44(6):1123-31. doi: 10.1016/j.jbiomech.2011.01.024.

Abstract

To investigate the effects of both non-Newtonian behavior and the pulsation of blood flow on the distributions of luminal surface LDL concentration and oxygen flux along the wall of the human aorta, we numerically compared a non-Newtonian model with the Newtonian one under both steady flow and in vivo pulsatile flow conditions using a human aorta model constructed from MRI images. The results showed that under steady flow conditions, although the shear thinning non-Newtonian nature of blood could elevate wall shear stress (WSS) in most regions of the aorta, especially areas with low WSS, it had little effect on luminal surface LDL concentration (c(w)) in most regions of the aorta. Nevertheless, it could significantly enhance c(w) in areas with high luminal surface LDL concentration through the shear dependent diffusivity of LDLs. For oxygen transport, the shear thinning non-Newtonian nature of blood could slightly reduce oxygen flux in most regions of the aorta, but this effect became much more apparent in areas with already low oxygen flux. The pulsation of blood flow could significantly reduce c(w) and enhance oxygen flux in these disturbed places. In most other regions of the aorta, the oxygen flux was also significantly higher than that for the steady flow simulation. In conclusion, the shear shining non-Newtonian nature of blood has little effect on LDL and oxygen transport in most regions of the aorta, but in the atherogenic-prone areas where luminal surface LDL concentration is high and oxygen flux is low, its effect is apparent. Similar is for the effect of pulsatile flow on the transport of LDLs. But, the pulsation of blood flow can apparently affect oxygen flux in the aorta, especially in areas with low oxygen flux.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aorta / metabolism*
  • Aorta / physiopathology*
  • Atherosclerosis / blood*
  • Atherosclerosis / physiopathology*
  • Biological Transport
  • Blood Flow Velocity
  • Humans
  • Lipoproteins, LDL / metabolism
  • Models, Cardiovascular*
  • Oxygen / blood*

Substances

  • Lipoproteins, LDL
  • Oxygen