Effects of Pressure-Induced Stretch and Convection on Low-Density Lipoprotein and Albumin Uptake in the Rabbit Aortic Wall

Author:

Meyer Guy1,Merval Re´gine1,Tedgui Alain1

Affiliation:

1. INSERM U141 and IFR Circulation Lariboisie`re, Hoˆpital Lariboisie`re, Paris, France.

Abstract

The effects of pressure-driven convection and vessel wall stretching in the pressure-related changes in low-density lipoprotein (LDL) and albumin transport across the arterial wall were studied in vitro in freshly excised rabbit thoracic aorta held at in vivo length and pressurized at 70, 120, or 160 mm Hg for 30 minutes. External rigid polyester sleeves of various diameters (4, 5, or 6 mm) were passed around half of the arterial segments in order to prevent vessel distension during pressurization. The intraluminal solution contained 131 I-LDL and 125 I-albumin. The transmural distribution of relative concentrations of LDL (C LDL ) and albumin (C alb ) across the wall was determined in wrapped and unwrapped segments using a serial frozen-sectioning technique. In the unwrapped segments, C alb increased uniformly between 70 and 120 mm Hg ( P <.0001) but did not change significantly between 120 and 160 mm Hg (0.0063±0.0009 [n=4], 0.0520±0.0055 [n=9], and 0.0620±0.0071 [n=12], respectively). In contrast, C LDL increased markedly both between 70 and 120 mm Hg ( P <.001) and between 120 and 160 mm Hg ( P <.05) (0.0025±0.0005 [n=4], 0.0234±0.0029 [n=9], and 0.0393±0.0056 [n=12], respectively), with the increase being much more pronounced in the inner than in the outer media. In the segments wrapped with the 4-mm sleeves, both C LDL and C alb did not vary significantly between 70, 120, and 160 mm Hg. In the segments wrapped with the 5-mm sleeves, C LDL increased significantly between 120 and 160 mm Hg, whereas C alb did not vary significantly with increasing pressure. Our results demonstrate that (1) pressure-induced stretching of the arterial wall is a major determinant of arterial mass transport, and (2) pressure-driven convection accentuates LDL accumulation in the inner media, which may explain enhanced atherosclerosis in hypertension.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference28 articles.

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3. Mass transport, atherogenesis, and risk.

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