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PMID: 7903526 Published · ppublish English Journal Article

Evidence for a polarized efflux system in CACO-2 cells capable of modulating cyclosporin A transport.

Biochemical and biophysical research communications ·Vol. 197 ·No. 2 ·1993-12-15 ·Pages 360-5

Augustijns PF, Bradshaw TP, Gan LS, Hendren RW, Thakker DR

Abstract

The characteristics of cyclosporin A (CsA) transport across Caco-2 monolayers were investigated. CsA (0.25-5.0 microM) was transported in a time and concentration dependent manner. The total amount of apical (AP) to basolateral (BL) transport was non-linearly related to CsA concentration from 0.25 to 1 microM and was linear from about 1 to 5 microM. Average permeability coefficient (Papp) values obtained in the AP to BL direction showed CsA concentration (0.5 and 5.0 microM) dependence, whereas those of the reverse (BL to AP) process did not. Papp values for the AP to BL direction were also markedly lower. When the P-glycoprotein pump inhibitors, chlorpromazine and progesterone, were included in the transport medium we observed a significant increase in CsA (0.5 and 5.0 microM) transport from the AP to BL direction; transport was decreased in the reverse direction. This study suggests that CsA is transported across Caco-2 cells by passive diffusion, but that a polarized efflux system (presumably a P-glycoprotein pump) located at the apical membrane can attenuate the net AP to BL transport.

MeSH Terms
ATP Binding Cassette Transporter, Subfamily B, Member 1 Adenocarcinoma Biological Transport/drug effects Carrier Proteins/antagonists & inhibitors Cell Line Cell Membrane/metabolism Chlorpromazine/pharmacology Colonic Neoplasms Cyclosporine/metabolism Drug Resistance Humans Kinetics Membrane Glycoproteins/antagonists & inhibitors Progesterone/pharmacology Tritium Tumor Cells, Cultured
Chemicals
ATP Binding Cassette Transporter, Subfamily B, Member 1 Carrier Proteins Membrane Glycoproteins Tritium Progesterone Cyclosporine Chlorpromazine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Augustijns P F
Drug Metabolism Department, Glaxo Inc. Research Institute, Research Triangle Park, North Carolina 27709.
Bradshaw T P
Gan L S
Hendren R W
Thakker D R
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1993-12-15
Pages
360-5
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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