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Issue title: Special Issue for the Fifth International Congress of Biorheology. Part II. Baden-Baden, F.R. Germany, 20–24 August 1983
Guest editors: Alfred L. Copley and Siegfried Witte
Article type: Research Article
Authors: Chien, Shu | Fan, Foun-chung | Lee, Mary M.L. | Handley, Dean A.
Affiliations: Division of Circulatory Physiology and Biophysics, Department of Physiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032
Abstract: The effects of variations in transmural pressure over a range of 0 to 200 mmHg on transendothelial transport of macromolecules were studied in the canine common carotid artery. The uptake of 125I-albumin per unit artery weight increased with rising pressure. There was no significant difference in albumin permeability per unit luminal surface area between 0 and 100 mmHg, but permeability nearly doubled when pressure was raised to 200 mmHg. The contribution of an increased rate of transendothelial vesicle diffusion, as evaluated from the experimental determination of the ratio of attached-to-free vesicles and theoretical modeling, was found to be negligible. The reduction in transendothelial vesicle diffusion distance due to pressure-induced thinning of the peripheral zone contributes to a 25% increase in permeability. with the use of colloidal Ag and Au of various sizes, vesicle loading of particles with diameters ⩾ 15 nm was found to be severely restricted at transmural pressure ⩽ 100 mmHg, but it was significantly enhanced at 200 mmHg, when particles as large as 25 nm became detectable in endothelial vesicles and subendothelial space. This hypertension-induced increase in macromolecular transport across the endothelium may cause an overloading of the arterial wall with low-density lipoproteins and play a significant role in atherogenesis.
Keywords: Albumin, Atherogenesis, Endothelium, Hypertension, Permeability, Vesicles
DOI: 10.3233/BIR-1984-21420
Journal: Biorheology, vol. 21, no. 4, pp. 631-641, 1984
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