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First published on December 1, 2006; DOI: 10.1124/dmd.106.010405


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Keisuke Mitsuoka
Yukio Kato
Yoshiyuki Kubo
Akira Tsuji
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Received for publication April 17, 2006.
Revised November 22, 2006.
Accepted for publication November 27, 2006.

Functional expression of stereoselective metabolism of cephalexin by exogenous transfection of oligopeptide transporter PEPT1

Keisuke Mitsuoka 1, Yukio Kato 1, Yoshiyuki Kubo 1, Akira Tsuji 1*

1 Kanazawa University

* Address correspondence to: E-mail: tsuji{at}kenroku.kanazawa-u.ac.jp

Abstract

Gastrointestinal absorption of the {beta}-lactam antibiotic cephalexin (CEX) is highly stereoselective: L- and D-CEX are both taken up by intestinal epithelial cells through the brush-border membrane, most likely via oligopeptide transporter PEPT1, but L-CEX is not found in serum or urine after oral administration due to its rapid intestinal metabolism, whereas D-CEX is well absorbed in the unchanged form. We examined the contribution of PEPT1 to the stereoselective uptake and metabolism of CEX. We observed stereoselective metabolism of CEX after exogenous transfection of PEPT1 alone into mammalian cell lines: L-CEX, but not D-CEX, was metabolized to 7-aminodesacetoxycephalosporanic acid (7-ADCA) in HeLa and HEK293 cells stably and transiently expressing human PEPT1, respectively, whereas such metabolism was minor in cells expressing the vector alone. The formation rate of 7-ADCA depended on the amount of PEPT1 cDNA transfected. L-CEX metabolism was rapid, since only 7-ADCA was found inside and outside the cells during incubation with L-CEX. The characteristics of PEPT1-mediated metabolism of L-CEX were similar, but not identical, to those of PEPT1-mediated transport. PEPT1-mediated metabolism was also observed in permeabilized cells expressing PEPT1, in which PEPT1-mediated intracellular substrate accumulation was negligible, suggesting that the increase in L-CEX metabolism by PEPT1 transfection cannot be fully explained by an increase in uptake and subsequent exposure to intracellular hydrolases. The present findings demonstrate that stereoselectivity in CEX absorption can be fully explained in terms of PEPT1, implying that the L-CEX hydrolase is PEPT1 itself, or is induced by PEPT1.


Key words: absorption, drug absorption, intestinal transport, membrane transport, transporters





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