Induction by verapamil of a rapid increase in ATP consumption in multidrug-resistant tumor cells

FASEB J. 1988 Apr;2(7):2278-82. doi: 10.1096/fasebj.2.7.3350243.

Abstract

A marked increase in cellular ATP consumption was induced by verapamil in the multidrug-resistant (MDR) cell line 2780AD, but not in the drug-sensitive parental cell line A2780. A group of structurally unrelated drugs in concentrations known to reverse MDR, but not the verapamil analog tiapamil, a weak modulator of MDR, had similar effects. This effect was saturated at verapamil concentrations of about 1 microM. These data demonstrate that verapamil concentrations in MDR cells are maintained at a low level at the expense of ATP hydrolysis, and provide a first indication of the amount of metabolic energy used in this process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Daunorubicin / metabolism
  • Drug Resistance
  • Female
  • Humans
  • Hydrolysis
  • Osmolar Concentration
  • Ovarian Neoplasms / pathology
  • Phenotype
  • Tumor Cells, Cultured / metabolism*
  • Verapamil / metabolism
  • Verapamil / pharmacology*
  • Vincristine / metabolism

Substances

  • Vincristine
  • Adenosine Triphosphate
  • Verapamil
  • Daunorubicin