Secretory transport of cadmium through intestinal brush border membrane via H+-antiport

Citation
T. Endo et al., Secretory transport of cadmium through intestinal brush border membrane via H+-antiport, TOXICOLOGY, 150(1-3), 2000, pp. 129-136
Citations number
35
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGY
ISSN journal
0300483X → ACNP
Volume
150
Issue
1-3
Year of publication
2000
Pages
129 - 136
Database
ISI
SICI code
0300-483X(20000907)150:1-3<129:STOCTI>2.0.ZU;2-S
Abstract
The effect of pH on the secretory transport of Cd through the intestinal br ush border membrane was investigated using isolated rat intestinal brush bo rder membrane vesicles (BBMV) and the Caco-2 intestinal epithelial cell lin e. BBMV equilibrated at pH 5.5 or 7.5 (pH(m)) were mixed with an experiment al buffer at pH 5.5 or 7.5 (pH(out)) containing CdCl2. The initial accumula tion of Cd in BBMV incubated for 1 or 3 min at pH(in) 5.5 and pH(out) 7.5 ( outwardly directed H+-gradient) was significantly higher than that at pH(in ) = pH(out) = 7.5, but the equilibrated Cd accumulation incubated for 30 mi n was marginally lower. Carbonylcyanide-p-trifluoromethoxyphenylhydrazone ( FCCP), a protonophore, diminished the increasing effect of the H+-gradient on the initial Cd accumulation. Caco-2 cell monolayers cultured on permeabl e membranes were incubated with CdCl2 from the basolateral medium, and the transport of Cd from the basolateral to apical medium and the accumulation of Cd in the monolayers were measured. Cd transport was increased by loweri ng the pH of the apical medium, and was accompanied by a decrease in the Cd accumulation. Coincubation with CdCl2 and tetraethylammonium, a typical, s ubstrate for H+-antiport of the renal organic cation transporter, from the basolateral medium slightly but significantly decreased the basolateral-to- apical transport of Cd, with a concomitant increase in the Cd accumulation. These findings suggest the secretory transport of Cd through the intestina l brush border membrane not only via passive diffusion but also via H+-anti port of the putative organic cation transporter. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.