期刊
INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷 210, 期 1-2, 页码 29-44出版社
ELSEVIER
DOI: 10.1016/S0378-5173(00)00564-0
关键词
ACE inhibitors; Caco-2 cells; dipeptide transporter system (DTS); dipeptides; peptidomimetic agents; structure-activity relationships
Purpose: To assess the affinities of a series of ACE inhibitors for the di/tri/oligopeptide transport system (DTS) using a rapid in vitro system. Methods: Monolayers of Caco-2 cells were cultured in plastic wells for 7-9 days and the uptake of Gly-[H-3]r-Pro was used as an affinity probe. Gly-[H-3]L-Pro (50 nM), together with excess L-Pro (10 mM), to suppress uptake of any [H-3]L-Pro produced by degradation of the probe, was incubated with the test compound (usually 1 mM) at pH 6 for 3-mins. The uptake of radiolabel was determined by liquid scintillation counting. Results: A 2-dimensional six-domain model of the transporter based on the structure of a phosphinate ACE inhibitor (SQ-29852) was constructed to facilitate interpretation of the competitor affinities. The SQ-29852 molecule was divided into six binding domains (A-F) based on functional groups within these regions and the effects of structural variation in four of these domains (A, C-E) were explored. A series of dipeptide-like compounds varying within specific domains were selected from a large number of commercially available ACE inhibitors and SQ-29852 analogues. Domain A had a preference for an uncharged group, with bulky hydrophobic groups reducing affinity. Domain C exhibited a preference for a positive charge over a neutral function, with the space this functional group occupies contributing to affinity. Domain D favoured lipophilic residues and domain E retained activity when the carboxylic acid was esterified. Conclusion: The test system is able to reveal structure-activity relationships of peptidomimetic agents and may well serve as a design tool to optimise affinity for the DTS. (C) 2000 Elsevier Science B.V. All rights reserved.
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