Rapid induction of P-glycoprotein expression by high permeability compounds in colonic cells in vitro: A possible source of transporter mediated drug interactions?

Andrew Collett, Jolanta Tanianis-Hughes, Geoff Warhurst

    Research output: Contribution to journalArticlepeer-review

    Abstract

    P-glycoprotein (PGP) substrates with high membrane permeability, such as propranolol and verapamil, are considered to be essentially " transparent" to PGP since the transporter does not significantly limit their absorption or elimination. However, the question of whether such compounds can modulate PGP expression in epithelial cells following short-term exposure, with potential consequences for drug interactions, has not been addressed. LS180 colonic epithelial cells were exposed to propranolol or verapamil at concentrations (50-300 μM) consistent with those likely to be present in the gut lumen during oral dosing. Both compounds stimulated four to six-fold increases in MDR1 mRNA and PGP protein expression measured by quantitative real-time PCR and immunoblotting, respectively. These changes were accompanied by an induction in transporter activity measured by rhodamine 123 efflux. In contrast, metoprolol, a compound with similar permeability but no affinity for PGP had no effect on PGP expression. The induction of PGP by propranolol and verapamil was rapid with significant increases occurring within 3 h with maximal stimulation after 6 h exposure. Rifampicin, shown to cause clinical drug interactions via a PXR-mediated increase in PGP expression, exhibited a very similar time-course and extent of induction. In conclusion, verapamil and propranolol, whose trans-epithelial permeability are unaffected by PGP, appear to be effective inducers of PGP expression in gut epithelial cells in vitro. While the in vivo significance of these observations is unknown, this questions whether high permeability, "PGP-transparent" compounds, currently favoured in drug selection strategies, should be evaluated in terms of their potential for transporter-mediated drug interactions. © 2004 Elsevier Inc. All rights reserved.
    Original languageEnglish
    Pages (from-to)783-790
    Number of pages7
    JournalBiochemical Pharmacology
    Volume68
    Issue number4
    DOIs
    Publication statusPublished - 15 Aug 2004

    Keywords

    • Drug absorption
    • Drug permeability
    • LS-180 cells
    • P-glycoprotein
    • Transporter induction

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