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Riboflavin uptake by rat small intestinal brush border membrane vesicles: A dual mechanism involving specific membrane binding
Authors:D. Casirola  G. Gastaldi  G. Ferrari  S. Kasai  G. Rindi
Affiliation:(1) Institute of Human Physiology, University of Pavia, Via Forlanini 6, 27100 Pavia, Italy;(2) Faculty of Engineering, Osaka City University, 558 Osaka, Japan
Abstract:The first step of riboflavin absorption was studied by determining the uptake of the vitamin by rat small intestinal brush border membrane vesicles. Vesicles were incubated at 25°C in the presence of [3H]-riboflavin at concentrations within the physiological intraluminal range for rat. The time course of [3H]-riboflavin uptake was unaffected by Na+ or K+ gradients. The 5 sec uptake rate plotted as a function of the initial concentration of [3H]-riboflavin in the medium (0.125 to 7.5 mgrm) revealed the presence of a dual mechanism, with a saturable component (apparent kinetic constants: 0.12 mgrm for Km and 0.36 pmol · mg-1 protein · 5 sec-1 for Jmax) prevailing at low concentrations (<2 mgrm), and a nonsaturable component prevailing at higher concentrations. The presence of a carrier-mediated system for riboflavin was validated by counter-transport experiments. At equilibrium, uptake was almost completely accounted for by membrane binding, whereas at earlier times the transport component accounted for about 30% of total uptake. The plot of [3H]-riboflavin binding at equilibrium as a function of its concentration in the medium was quite similar to that of the 5 sec uptake rate in both intact and osmotically shocked vesicles and demonstrated the occurrence of a saturable component: binding constants were 0.07 (Kd) in mgrm), 0.54 (Bmax in pmol · mg-1 protein), and 0.11 (Kd), 1.13 (Bmax, respectively, indicating the existence of specific riboflavin binding sites. The specificity of riboflavin binding to the membrane was confirmed by preliminary studies with structural analogues. Specific binding could represent the first step of a specific riboflavin entry mechanism in enterocytes.This research was supported by grants from Italian MPI 60% (1989, 1992) and CNR n. 90, 02467 CT 04. We wish to express our gratitude to Prof. E. Perucca (Department of Internal Medicine, Clinical Pharmacology Unit, University of Pavia) for revising the English, and to Mrs. M. Agrati Greco and Mrs. P. Vai Gatti for secretarial assistance and excellent typing.
Keywords:Intestinal brush border vesicles  Riboflavin  Transport  Binding
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