Journal article

Drug specificity and intestinal membrane localization of human organic cation transporters (OCT)


Authors listMüller, J; Lips, KS; Metzner, L; Neubert, RHH; Koepsell, H; Brandsch, M

Publication year2005

Pages1851-1860

JournalBiochemical Pharmacology

Volume number70

Issue number12

ISSN0006-2952

eISSN1873-2968

DOI Linkhttps://doi.org/10.1016/j.bcp.2005.09.011

PublisherElsevier


Abstract
This study was performed to investigate which human organic cation transporter, hOCT1, hOCT2 or hOCT3, participates with regard to cation specificity and membrane localization in the intestinal absorption of orally available cationic drugs. Inhibition of N-[methyl-H-3]4-phenylpyridinium ([H-3]MPP+) uptake by various compounds into Caco-2 cells and into cells (HEK-293 or CHO) that were stably transfected with hOCT1, hOCT2 or hOCT3 was compared. The uptake of [H-3]MPP+ into Caco-2 cells was inhibited by atropine, butylscopolamine, clonidine, diphenhydramine, etilefrine, quinine and ranitidine with IC50 values between 6 mu M and 4 mM. Transepithelial, apical to basal flux of [H-3]MPP+ across Caco-2 cell monolayers was also strongly inhibited by these compounds. The inhibitory potency of the cationic drugs and prototypical organic cations at Caco-2 cells correlated well with the inhibitory potency measured at CHO-hOCT3 cells but much less with that at HEK-hOCT1 and -hOCT2 cells. This is functional evidence for the predominant role of hOCT3. Etilefrine and atropine were specifically transported into CHO cells by hOCT3. In Caco-2 cells, the mRNA of all three hOCT and the proteins hOCT2 and hOCT3 were detected. More importantly, immunocytochemical analyses of human jejunum revealed for the first time that hOCT3 is localized to the brush border membrane whereas hOCT1 immunolabeling was mainly observed at the lateral membranes of the enterocytes. (c) 2005 Elsevier Inc. All rights reserved.



Citation Styles

Harvard Citation styleMüller, J., Lips, K., Metzner, L., Neubert, R., Koepsell, H. and Brandsch, M. (2005) Drug specificity and intestinal membrane localization of human organic cation transporters (OCT), Biochemical Pharmacology, 70(12), pp. 1851-1860. https://doi.org/10.1016/j.bcp.2005.09.011

APA Citation styleMüller, J., Lips, K., Metzner, L., Neubert, R., Koepsell, H., & Brandsch, M. (2005). Drug specificity and intestinal membrane localization of human organic cation transporters (OCT). Biochemical Pharmacology. 70(12), 1851-1860. https://doi.org/10.1016/j.bcp.2005.09.011



Keywords


APICAL UPTAKECACO-2 CELL MONOLAYERScationic therapeutic drugsOCT3PEPT1ROCT1stably transfected cell lines

Last updated on 2025-18-06 at 13:48