Interstitial flow through the internal elastic lamina affects shear stress on arterial smooth muscle cells.

Interstitial flow through the tunica media of an artery wall in the presence of the internal elastic lamina (IEL), which separates it from the subendothelial intima, has been studied numerically. A two-dimensional analysis applying the Brinkman model as the governing equation for the porous media flow field was performed. In the numerical simulation, the IEL was modeled as an impermeable barrier to water flux, except for the fenestral pores, which were uniformly distributed over the IEL. The tunica media was modeled as a heterogeneous medium composed of a periodic array of cylindrical smooth muscle cells (SMCs) embedded in a fiber matrix simulating the interstitial proteoglycan and collagen fibers. A series of calculations was conducted by varying the physical parameters describing the problem: the area fraction of the fenestral pore (0. 001-0.036), the diameter of the fenestral pore (0.4-4.0 microm), and the distance between the IEL and the nearest SMC (0.2-0.8 microm). The results indicate that the value of the average shear stress around the circumference of the SMC in the immediate vicinity of the fenestral pore could be as much as 100 times greater than that around an SMC in the fully developed interstitial flow region away from the IEL. These high shear stresses can affect SMC physiological function.

[1]  S. Weinbaum,et al.  Structural changes in rat aortic intima due to transmural pressure. , 1998, Journal of biomechanical engineering.

[2]  S. Glagov,et al.  Flow regulation of 72-kD collagenase IV (MMP-2) after experimental arterial injury. , 1998, Circulation.

[3]  L. McIntire,et al.  Nitric oxide production by cultured human aortic smooth muscle cells: stimulation by fluid flow. , 1998, American journal of physiology. Heart and circulatory physiology.

[4]  C. T. Wagner,et al.  Hemodynamic forces induce the expression of heme oxygenase in cultured vascular smooth muscle cells. , 1997, The Journal of clinical investigation.

[5]  T. Yaginuma,et al.  Shear stress as an inhibitor of vascular smooth muscle cell proliferation. Role of transforming growth factor-beta 1 and tissue-type plasminogen activator. , 1997, Arteriosclerosis, thrombosis, and vascular biology.

[6]  J. Tarbell,et al.  Numerical simulation of mass transfer in porous media of blood vessel walls. , 1997, The American journal of physiology.

[7]  J. Tarbell,et al.  Shear stress-induced release of PGE2 and PGI2 by vascular smooth muscle cells. , 1996, Biochemical and biophysical research communications.

[8]  J. Tarbell,et al.  Modeling interstitial flow in an artery wall allows estimation of wall shear stress on smooth muscle cells. , 1995, Journal of biomechanical engineering.

[9]  R. Lal,et al.  Subcellular distribution of shear stress at the surface of flow-aligned and nonaligned endothelial monolayers. , 1995, The American journal of physiology.

[10]  J A Frangos,et al.  Shear stress increases hydraulic conductivity of cultured endothelial monolayers. , 1995, The American journal of physiology.

[11]  S. Weinbaum,et al.  A fiber matrix model for the growth of macromolecular leakage spots in the arterial intima. , 1994, Journal of biomechanical engineering.

[12]  J. Tarbell,et al.  Macromolecular transport through the deformable porous media of an artery wall. , 1994, Journal of biomechanical engineering.

[13]  J. Gavin,et al.  The importance of a substantial elastic lamina subjacent to the endothelium in limiting the progression of atherosclerotic changes , 1993, Histopathology.

[14]  M. Gimbrone,et al.  Vascular endothelium responds to fluid shear stress gradients. , 1992, Arteriosclerosis and thrombosis : a journal of vascular biology.

[15]  A. Cucina,et al.  Response of arterial smooth muscle cells to laminar flow. , 1992, The Journal of cardiovascular surgery.

[16]  M. R. Roach,et al.  Arterial elastin as seen with scanning electron microscopy: a review. , 1988, Scanning microscopy.

[17]  M. Lever,et al.  Filtration through damaged and undamaged rabbit thoracic aorta. , 1984, The American journal of physiology.

[18]  R. Friedrich,et al.  Similar Solutions of Brinkman Equations for a Two-Dimensional Plane Jet in a Porous Medium , 1983 .

[19]  F. Curry,et al.  A fiber matrix model of capillary permeability. , 1980, Microvascular research.

[20]  H. Brinkman A calculation of the viscous force exerted by a flowing fluid on a dense swarm of particles , 1949 .

[21]  Herbert H. Lipowsky,et al.  Shear Stress in the Circulation , 1995 .

[22]  J. Bevan,et al.  Flow-Dependent Regulation of Vascular Function , 1995, Clinical Physiology Series.