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Vol. 298, Issue 2, 711-717, August 2001
Department of Pharmacy, Kyoto University Hospital, Faculty of
Medicine, Kyoto University, Kyoto, Japan
Recent studies have revealed that diverse compounds lacking
peptide bonds, such as valacyclovir and
-aminolevulinic acid (
-ALA), can be recognized by H+-coupled peptide
transporters (PEPT1 and PEPT2). In the present study, recognition and
transport characteristics of nonpeptidic compounds by the basolateral
peptide transporter, which is distinct from PEPTs, were compared with
those by PEPT1 using the human intestinal Caco-2 cells.
[14C]Glycylsarcosine uptake via PEPT1 was inhibited by
all nonpeptidic compounds tested. Similarly, most nonpeptidic compounds
showed an inhibitory effect on [14C]glycylsarcosine
uptake by the basolateral peptide transporter, although some kinds of
nonpeptidic compounds, such as valine methyl ester, did not. Direct
measurements of valacyclovir and
-ALA transport revealed that both
compounds were able to be transported by the basolateral peptide
transporter. Because
-ALA has been used recently in vitro and in
clinical studies as an endogenous photosensitizer for photodynamic
therapy, the intestinal transport characteristics of
-ALA were
further examined. Inhibition studies and Eadie-Hofstee plot analysis
suggested that
-ALA transport across the brush-border and
basolateral membranes of the intestine was mainly mediated by peptide
transporters. In addition, the apical-to-basolateral transport of
-ALA was greater than that of the opposite direction. These findings
provide the first evidence that the intestinal basolateral peptide
transporter can recognize and transport nonpeptidic compounds, and play
a definitive role in the absorption of
-ALA.
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