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D Winne

Publications and source records attributed to D Winne.

At least 37 records · Page 2Linked to original sources

Rat jejunum perfused in situ: effect of perfusion rate and intraluminal radius on absorption rate and effective unstirred layer thickness.

In anaesthetized rats a jejunal segment was perfused in situ varying the perfusion rate (0.1, 0.2, 0.5 ml/min) in a randomized order. The intraluminal radius of the segments was small (1.7 mm) or enlarged (3.1 mm) by increasing the intraluminal pressure. The appearance rate of butanol, antipyrine, salicylic acid, D- and L-phenylalanine but not of urea in the venous blood of the jejunal segments was increased up to 35%, when the intraluminal perfusion rate was raised from 0.1 to 0.5 ml/min. Two factors contribute to this effect: the flattening of the concentration gradient down the segment and the reduction of the effective unstirred layer thickness. The length and the intraluminal radius of the perfused segments was not altered, when the perfusion rate was varied. Therefore, a change of the absorbing area did not contribute to the increase of the absorption rate induced by the increase of the perfusion rate. In the series with small intraluminal radius the experimental data corresponded to the theoretical predictions obtained for a laminar intraluminal flow. In the segments with enlarged intraluminal radius the increase of the absorption rate by raising the perfusion rate was less than expected for a laminar flow indicating that the flow might have been turbulent. The enlargement of the intraluminal radius from 1.7 to 3.1 mm increased the absorption rate up to 100%.

Animals↗

Absorption and metabolism of naphthalene and benzo(a)pyrene in the rat jejunum in situ.

Naphthalene or benzo(a)pyrene (100 nmol) was instilled into the closed rat intestinal loop in situ and the appearance of the free compound and its metabolites was determined in portal blood. Naphthalene appeared mostly unchanged in blood whereas benzo(a)pyrene was extensively metabolized by mucosal cells. The results suggest that absorption and metabolism are competing processes in the gut.

Animals↗

The permeability coefficient of the wall of a villous membrane.

The equations hitherto used to correct the permeability coefficient for the unstirred layer influence are valid only for flat membranes. Therefore, appropriate equations for membranes with a villous surface (e.g., small intestine) have been derived. They take into account the non-linear concentration gradient in the intervillous part of the unstirred layer. Quantitative information about the geometry of the villous surface and the unstirred layer thickness are needed to calculate the permeability coefficient of the membrane wall (e.g., intestinal epithelium). The concentration of highly permeable substances drops sharply already in the upper part of intervillous space, so that the tips of the villi function as effective absorbing area. The intervillous concentration gradient of a substance with a low permeability coefficient is so small, that such a substance is absorbed by the total surface area of the villous membrane. The effective absorbing area of substances with intermediate permeability coefficient lies between the described limits.

Cell Membrane↗

Dependence of intestinal absorption in vivo on the unstirred layer.

The appearance rate of butanol, antipyrine, salicylic acid, and urea in the venous blood of rat jejunal loops perfused in vivo is increased up to 64%, if the intraluminal solution is mixed more efficiently by the simultaneous perfusion of air. The enhancement of the absorption can be attributed partly to the enlarged absorbing area but mainly to the reduction of the effective unstirred layer thickness by about 500 micrometers. The unstirred layer reduces the phenylalanine absorption at 0.1 mmol l(-1) but not at 100 mmol l(-1), since at high concentrations a full saturation of the transport system can be achieved in spite of the unstirred layer resistance. The interference of the unstirred layer increases with increasing absorbability of the substances.

Animals↗

Correction of the apparent Michaelis constant, biased by an unstirred layer, if a passive transport component is present.

An unstirred layer shifts the permeation curve due to a carrier-mediated transport system (non-passive component) to the right, so that a higher Km value is determined (apparent Michaelis constant biased by an unstirred layer). If a substance is transported simultaneously by a non-passive and a passive mechanism, and if the non-passive component can be inhibited, the permeation curve due to the non-passive component can be obtained by subtraction of the curve due to the passive component alone from the curve obtained with intact passive and non-passive component. But in the presence of an unstirred layer the difference curve lies always below the curve which would be obtained in the presence of the non-passive component alone. This error increases with increasing unstirred layer thickness and increasing magnitude of the passive transport component. By means of an appropriate equation the apparent Michaelis constant biased by an unstirred layer and determined from the difference curve can be corrected, if the unstirred layer thickness and area are known.

Biological Transport↗