Vol. 289, Issue 1, 346-353, April 1999

Cimetidine Transport in Brush-Border Membrane Vesicles from Rat Small Intestine¹

Nusara Piyapolrungroj, Cheng Li, Ronald L. Pisoni and David Fleisher

Faculty of Pharmacy, Silpakorn University, Nakorn-Pathom, Thailand (N.P.); College of Pharmacy, University of Michigan, Ann Arbor, Michigan (C.L., D.F.); University Renal Research and Education Associates, Ann Arbor, Michigan

In previous studies, sulfoxide metabolite was observed in animal and human intestinal perfusions of cimetidine and other H₂-antagonists. A sequence of follow-up studies is ongoing to assess the intestinal contributions of drug metabolism and drug and metabolite transport to variable drug absorption. An evaluation of these contributions to absorption variability is carried out in isolated fractions of the absorptive cells to uncouple the processes involved. In this report, data is presented on the drug entry step from a study on [³H]cimetidine uptake into isolated brush-border membrane vesicles from rat small intestine. A saturable component for cimetidine uptake was characterized with a V_max and K_m (mean ± S.E.M.) of 6.1 ± 1.5 nmol/30s/mg protein and 8.4 ± 2.0 mM, respectively. Initial binding, and possibly intravesicular uptake, was inhibited by other cationic compounds including ranitidine, procainamide, imipramine, erythromycin, and cysteamine but not by TEA or by the organic anion, probenecid. Initial uptake was not inhibited by amino acids methionine, cysteine, or histidine, by the metabolite cimetidine sulfoxide, or by inhibitors of cimetidine sulfoxidation, methimazole, and diisothiocyanostilbene-2,2'-disulfonic acid. Equilibrium uptake was inhibited by ranitidine, procainamide, and cysteamine but not by erythromycin or imipramine. Initial cimetidine uptake was stimulated by an outwardly directed H⁺ gradient, and efflux was enhanced by an inwardly directed H⁺ gradient. Collapse of the H⁺ gradient as well as voltage-clamping potential difference to zero significantly reduced initial cimetidine uptake. The data is supportive of both a cimetidine/H⁺ exchange mechanism and a driving-force contribution from an inside negative proton or cation diffusion potential.