AJP - Heart and Circulatory Physiology, Vol 271, Issue 3 1099-H1108, Copyright © 1996 by American Physiological Society

ARTICLES

Basal and adenosine-mediated protein flux from isolated coronary arterioles

V. H. Huxley and D. A. Williams
Department of Physiology, University of Missouri School of Medicine, Columbia 65212, USA. physfrog@muccmail.missouri.edu

We have developed a new method to quantify solute flux per unit surface area and concentration gradient (JS/S delta C) from arterioles isolated from pig hearts. The apparent permeability (Ps) was assessed from measurements of JS/S delta C for two proteins, alpha-lactalbumin (alpha-lactalb) and porcine serum albumin (PSA), labeled with the fluorescent dye tetramethylrhodamine isothiocyanate at a mean hydrostatic pressure of 16 +/- 1 cmH2O. Ps for alpha-lactalb (Ps alpha-lactalb) was 16.5 +/- 4.6 x 10(-7) cm/s (mean +/- SE, N = 8 pigs), a value significantly higher than Ps for PSA (PsPSA) (7.1 +/- 1.4 x 10(-7) cm/s, N = 11 pigs, P < 0.05). Suffusion of the arterioles (44 +/- 10 microns diam; n = 48 arterioles) with 10(-5) M adenosine resulted in a 35% decrease in Ps alpha-lactalb and 29% decrease in PsPSA. Data from the present study are consistent with adenosine altering arteriole Js independently from its ability to change arteriolar caliber. One implication of these results is that changes in coronary exchange capacity reflect not only changes in flow through, but also solute permeation from, the microvasculature.

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