Determination of p-glycoprotein ATPase activity using luciferase

Biol Pharm Bull. 2006 Mar;29(3):560-4. doi: 10.1248/bpb.29.560.

Abstract

We investigated whether P-glycoprotein (P-gp) ATPase activity of Caco-2 cell membranes could be estimated by measuring consumption of ATP using luciferin-luciferase reaction, and whether the results would be useful for assessment of the interactions between P-gp and drugs. The vanadate-sensitive ATPase activity of Caco-2 cell membranes was measured rapidly with high sensitivity using luciferin-luciferase reaction. Cyclosporin A, verapamil, digoxin and quinidine stimulated the ATPase activity concentration-dependently with Km values of 5.3, 0.9, 1.2 and 4.1 microM, respectively. These values except for digoxin were comparable with previous reports. The ATPase activity and P-gp mRNA expression in Caco-2 cells were induced by all-trans-retinoic acid, digoxin and levothyroxine, but not dexamethasone or rifampicin. This method was useful to assess interactions with P-gp and drugs, and was used to elucidate the mechanisms of interaction of levothyroxine and digoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / analysis*
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Adenosine Triphosphatases / analysis*
  • Adenosine Triphosphatases / metabolism
  • Adenosine Triphosphate / metabolism
  • Caco-2 Cells
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Dexamethasone / pharmacology
  • Digoxin / pharmacology
  • Glucocorticoids / pharmacology
  • Humans
  • Kinetics
  • Luciferases*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / isolation & purification
  • Rifampin / pharmacology
  • Thyroxine / pharmacology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Glucocorticoids
  • RNA, Messenger
  • Digoxin
  • Dexamethasone
  • Adenosine Triphosphate
  • Luciferases
  • Adenosine Triphosphatases
  • Thyroxine
  • Rifampin