|
|
||||||||
The FASEB Journal, Vol 2, 2278-2282, Copyright © 1988 by The Federation of American Societies for Experimental Biology
RESEARCH COMMUNICATIONS |
HJ Broxterman, HM Pinedo, CM Kuiper, LC Kaptein, GJ Schuurhuis and J Lankelma
Department of Oncology, Free University Hospital, Amsterdam, The Netherlands.
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.
This article has been cited by other articles:
![]() |
R. W. Johnstone, E. Cretney, and M. J. Smyth P-Glycoprotein Protects Leukemia Cells Against Caspase-Dependent, but not Caspase-Independent, Cell Death Blood, February 1, 1999; 93(3): 1075 - 1085. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. D. Eytan, R. Regev, and Y. G. Assaraf Functional Reconstitution of P-glycoprotein Reveals an Apparent Near Stoichiometric Drug Transport to ATP Hydrolysis J. Biol. Chem., February 9, 1996; 271(6): 3172 - 3178. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |