Carrier-mediated uptake of cisplatin by the OK renal epithelial cell line

被引:44
作者
Endo, T [1 ]
Kimura, O [1 ]
Sakata, M [1 ]
机构
[1] Hlth Sci Univ Hokkaido, Fac Pharmaceut Sci, Ishikari, Hokkaido 0610293, Japan
关键词
cisplatin; OK cells; organic cation transporter; tetraethylammonium; apical membrane; basolateral membrane;
D O I
10.1016/S0300-483X(00)00176-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to investigate whether transport of cis-diamminedichloroplatinum II (cisplatin) across renal epithelial cell line OK cells is mediated by the organic cation transport system. OK cell monolayers cultured on permeable membranes were incubated with 100 mu M cisplatin on the apical or basolateral side, and the cellular accumulation and the transport of cisplatin across the monolayer were measured. The accumulation from the basolateral medium and the basolateral-to-apical transport of cisplatin were higher than the accumulation from the apical medium and the apical-to-basolateral transport, respectively. The cell monolayers were incubated with different concentrations of cisplatin (0.02 similar to 3 mM) in the basolateral medium. The relationship between the cisplatin concentrations in the medium and in the cells revealed that cisplatin accumulation tended to be saturable. The basolateral-to-apical transport of cisplatin was increased when the pH of the apical medium was decreased, with a concomitant decrease in the accumulation of cisplatin. Coincubation of cisplatin with tetraethylammonium (TEA), a typical substrate for the organic cation transporter, significantly decreased the accumulation and transport of cisplatin From the basolateral medium. These results suggest that the uptake and basolateral-to-apical transport of cisplatin are mediated by not only simple diffusion but also by the organic cation transport system. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:187 / 195
页数:9
相关论文
共 28 条
[1]  
BIRD JE, 1984, J PHARMACOL EXP THER, V231, P752
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   PLATINUM COMPLEX-INDUCED DYSFUNCTION OF CULTURED RENAL PROXIMAL TUBULE CELLS - A COMPARATIVE-STUDY OF CARBOPLATIN AND TRANSPLATIN WITH CISPLATIN [J].
COURJAULT, F ;
LEROY, D ;
COQUERY, I ;
TOUTAIN, H .
ARCHIVES OF TOXICOLOGY, 1993, 67 (05) :338-346
[4]   THE RENAL FRACTIONAL CLEARANCE OF PLATINUM ANTITUMOUR COMPOUNDS IN RELATION TO NEPHROTOXICITY [J].
DALEYYATES, PT ;
MCBRIEN, DCH .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (09) :1423-1428
[5]  
DOBYAN DC, 1980, J PHARMACOL EXP THER, V213, P551
[6]   Bidirectional transport of cadmium across apical membrane of renal epithelial cell lines via H+-antiporter and inorganic anion exchanger [J].
Endo, T ;
Kimura, O ;
Sakata, M .
TOXICOLOGY, 1998, 131 (2-3) :183-192
[7]  
Endo T, 1995, BIOL PHARM BULL, V18, P1689
[8]   Comparative studies of cadmium and mercury accumulation by LLC-PK1 cells: Effects of pH on uptake and efflux [J].
Endo, T ;
Kimura, O ;
Sakata, M .
TOXICOLOGY LETTERS, 1996, 87 (2-3) :77-83
[9]   Effects of zinc and copper on cadmium uptake by brush border membrane vesicles [J].
Endo, T ;
Kimura, O ;
Hatakeyama, M ;
Takada, M ;
Sakata, M .
TOXICOLOGY LETTERS, 1997, 91 (02) :111-120
[10]   CELLULAR ACCUMULATION OF THE ANTICANCER AGENT CISPLATIN - A REVIEW [J].
GATELY, DP ;
HOWELL, SB .
BRITISH JOURNAL OF CANCER, 1993, 67 (06) :1171-1176