In vitro Study of Starling’s Hypothesis in a Cultured Monolayer of Bovine Aortic Endothelial Cells

Starling’s hypothesis that fluid movement across the microvascular wall is determined by the transmural differences in hydrostatic and osmotic pressures was tested using an in vitro model comprised of bovine aortic endothelial cells grown on a porous support. In all experiments, a 1% bovine serum albumin (BSA) solution was maintained in the abluminal reservoir and the luminal reservoir contained either a 1 or a 5.5% BSA solution. The global osmotic pressure difference across the endothelial layers was thus either 0 or 20.3 cm H2O. When the luminal concentration of BSA was changed from 1 to 5.5% at a hydrostatic pressure differential of 5, 10 or 20 cm H2O, no reverse flow (in the reabsorption direction) was observed even though the hydrostatic pressure differential was far below the global osmotic pressure differential. In another case, the hydrostatic pressure differential was dropped quickly from 20 to 5 cm H2O, while a constant osmotic pressure differential was maintained by 5.5% BSA in the luminal reservoir. A strong transient reabsorption flow was observed over a 30-second period which diminished to undetectable levels within 2.5 min; then a sustained steady-state filtration flow was observed after 20 min. These in vitro experiments support other studies in capillaries showing transient reabsorption that decays to steady-state filtration at longer times.

[1]  J. Tarbell,et al.  Oscillatory shear alters endothelial hydraulic conductivity and nitric oxide levels. , 2002, Biochemical and biophysical research communications.

[2]  S. Weinbaum,et al.  Starling forces that oppose filtration after tissue oncotic pressure is increased. , 2000, American journal of physiology. Heart and circulatory physiology.

[3]  T W Gardner,et al.  Effect of vascular endothelial growth factor on cultured endothelial cell monolayer transport properties. , 2000, Microvascular research.

[4]  S. Weinbaum,et al.  A new view of Starling's hypothesis at the microstructural level. , 1999, Microvascular research.

[5]  J. Tarbell,et al.  Effect of pressure on hydraulic conductivity of endothelial monolayers: role of endothelial cleft shear stress. , 1999, Journal of applied physiology.

[6]  Sheldon Weinbaum,et al.  1997 Whitaker Distinguished Lecture: Models to Solve Mysteries in Biomechanics at the Cellular Level; A New View of Fiber Matrix Layers , 1998, Annals of Biomedical Engineering.

[7]  V. Huxley,et al.  Basal and adenosine-mediated protein flux from isolated coronary arterioles. , 1996, The American journal of physiology.

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

[9]  J. Tarbell,et al.  Albumin permeability and electrical resistance as means of assessing endothelial monolayer integrity in vitro , 1992 .

[10]  Levick Capillary filtration‐absorption balance reconsidered in light of dynamic extravascular factors , 1991, Experimental physiology.

[11]  J. Tarbell,et al.  The effect of varying albumin concentration and hydrostatic pressure on hydraulic conductivity and albumin permeability of cultured endothelial monolayers. , 1991, Microvascular research.

[12]  C G Caro,et al.  The effect of varying albumin concentration of the hydraulic conductivity of the rabbit common carotid artery. , 1988, Microvascular research.

[13]  D. Shasby,et al.  Effects of albumin concentration on endothelial albumin transport in vitro. , 1987, American Journal of Physiology.

[14]  C. Michel,et al.  Steady‐state fluid filtration at different capillary pressures in perfused frog mesenteric capillaries. , 1987, The Journal of physiology.

[15]  V. Huxley,et al.  Effect of superfusate albumin on single capillary hydraulic conductivity. , 1987, The American journal of physiology.

[16]  J. Cooper,et al.  Transendothelial albumin flux: evidence against asymmetric transport. , 1986, Journal of applied physiology.

[17]  D A Goldstein,et al.  The flow of solute and solvent across a two-membrane system. , 1963, Journal of theoretical biology.

[18]  E. Starling On the Absorption of Fluids from the Connective Tissue Spaces , 1896, The Journal of physiology.

[19]  C. Michel,et al.  Starling: the formulation of his hypothesis of microvascular fluid exchange and its significance after 100 years , 1997, Experimental physiology.

[20]  B. Zweifach,et al.  Microcirculatory basis of fluid exchange. , 1974, Advances in biological and medical physics.

[21]  O. Bailey Advances in Biological and Medical Physics , 1962 .