Demonstration of the activity of P-glycoprotein by a semi-automated fluorometric method

Anticancer Res. 2009 Jun;29(6):2173-7.

Abstract

Background: We have developed a semi-automated fluorometric method that utilizes ethidium bromide (EB), a common substrate of bacterial efflux pumps. The method is sufficiently sensitive to characterize the efflux pump systems of bacteria. Because EB is also recognized and extruded by ATP-binding cassette (ABC) transporters and these have similarity to P-glycoprotein (P-gp), the method has been extended for the evaluation of agents that can inhibit the extrusion of EB on a real-time basis by mouse lymphoma cells containing the human ABCB1 (mdr1) gene.

Materials and methods: Monitoring of uptake and extrusion of EB was assessed using the Rotor-Gene 3000 (Corbett Research) under different conditions.

Results: Whereas extrusion of EB took place readily, the addition of known inhibitors of efflux pumps (verapamil, reserpine) caused retention of EB.

Conclusion: This method is inexpensive and allows the detection of neoplastic cells with increased efflux activity as well as the screening of large numbers of compounds for inhibition of the P-gp.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Adrenergic Uptake Inhibitors / pharmacology
  • Animals
  • Automation
  • Biological Transport / drug effects
  • Calcium Channel Blockers / pharmacology
  • Cell Survival / drug effects
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Ethidium / metabolism*
  • Fluorometry
  • Humans
  • Lymphoma, T-Cell / metabolism*
  • Mice
  • Reserpine / pharmacology
  • Verapamil / pharmacology

Substances

  • ABCB1 protein, human
  • ATP Binding Cassette Transporter, Subfamily B
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Adrenergic Uptake Inhibitors
  • Calcium Channel Blockers
  • Reserpine
  • Verapamil
  • Ethidium