PSC833, cyclosporin A, and dexniguldipine effects on cellular calcein retention and inhibition of the multidrug resistance pump in human leukemic lymphoblasts

Biochem Biophys Res Commun. 1999 Apr 13;257(2):410-3. doi: 10.1006/bbrc.1999.0475.

Abstract

A convenient functional assay of the multidrug resistance (MDR) pump is useful for the diagnosis of MDR-1 cancers and the quantitative determination of the potency of inhibitors of the pump. Calcein-AM, a substrate of the MDR pump, was used to determine the concentration of SDZ PSC833 needed to completely inhibit the pump in CEM/VLB100 drug-resistant cells. The initial rates (in percent) for calcein retention by these MDR-1 cells were used to calculate values for the percent initial efflux of calcein-AM through the MDR pump in the presence of the inhibitors PSC833, cyclosporinA, and dexniguldipine. The percent efflux values at 250 and 60 nM calcein-AM were used to calculate the required concentration of each inhibitor to produce half-inhibition (I50) of initial efflux through the pump. These results are consistent with a noncompetitive inhibition of the MDR pump by each of the three inhibitors.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / antagonists & inhibitors*
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Cyclosporine / pharmacology*
  • Cyclosporins / pharmacology*
  • Dihydropyridines / pharmacology*
  • Drug Resistance, Neoplasm
  • Fluoresceins / metabolism*
  • Fluoresceins / pharmacokinetics
  • Half-Life
  • Humans
  • Inhibitory Concentration 50
  • Kinetics
  • Leukemia / diagnosis
  • Leukemia / metabolism*
  • Leukemia / pathology
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism
  • Molecular Weight
  • Tumor Cells, Cultured

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Cyclosporins
  • Dihydropyridines
  • Fluoresceins
  • calcein AM
  • Cyclosporine
  • valspodar
  • niguldipine