In-vitro respiratory drug absorption models possess nominal functional P-glycoprotein activity

J Pharm Pharmacol. 2009 Mar;61(3):293-301. doi: 10.1211/jpp/61.03.0003.

Abstract

Objectives: The P-glycoprotein (P-gp) efflux pump is known to be present within several major physiological barriers including the brain, kidney, intestine and placenta. However, the function of P-gp in the airways of the lung is unclear. The purpose of this study was to use the highly specific P-gp inhibitor GF120918A to investigate the activity of the P-gp transporter in the airways to determine whether P-gp could influence inhaled drug disposition.

Methods: P-gp activity was measured as a change in digoxin transport in the presence of GF120918A in normal human bronchial epithelial (NHBE) cells, Calu-3 cell layers and the ex-vivo rat lung.

Key findings: The efflux ratios (ERs) in NHBE and Calu-3 cells were between 0.5 and 2, in contrast to 10.7 in the Caco-2 cell control. These low levels of GF120918A-sensitive polarised digoxin transport were measured in the absorptive direction in NHBE cells (ER = 0.5) and in the secretory direction in Calu-3 cells (ER = 2), but only after 21 days in culture for both cell systems and only in Calu-3 cells at passage > 50. The airspace to perfusate transfer kinetics of digoxin in the ex-vivo rat lung were unchanged in the presence of GF120918A.

Conclusions: These results demonstrated that although low levels of highly culture-dependent P-gp activity could be measured in cell-lines, these should not be interpreted to mean that P-gp is a major determinant of drug disposition in the airways of the lung.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / antagonists & inhibitors
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Acridines / pharmacology
  • Administration, Inhalation
  • Animals
  • Biological Transport
  • Bronchi / cytology
  • Bronchi / metabolism
  • Caco-2 Cells
  • Cells, Cultured
  • Digoxin / administration & dosage
  • Digoxin / pharmacokinetics*
  • Epithelial Cells / metabolism
  • Humans
  • Lung / metabolism*
  • Male
  • Models, Biological*
  • Rats
  • Rats, Wistar
  • Tetrahydroisoquinolines / pharmacology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Acridines
  • Tetrahydroisoquinolines
  • Digoxin
  • Elacridar