Diphenhydramine transport by pH-dependent tertiary amine transport system in Caco-2 cells

被引:37
作者
Mizuuchi, H [1 ]
Katsura, T [1 ]
Ashida, K [1 ]
Hashimoto, Y [1 ]
Inui, KI [1 ]
机构
[1] Kyoto Univ Hosp, Dept Pharm, Sakyo Ku, Fac Med, Kyoto 6068507, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2000年 / 278卷 / 04期
关键词
organic cation; intestinal absorption; intestinal secretion; hydrogen/organic cation antiport system;
D O I
10.1152/ajpgi.2000.278.4.G563
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Substrate specificity and pH dependence of the transport system for diphenhydramine were investigated in Caco-2 cell monolayers. Diphenhydramine uptake was not affected by any typical substrate for the renal organic cation transport system except procainamide. Along with procainamide, tertiary amine compounds with N-dimethyl or N-diethyl moieties in their structures inhibited the diphenhydramine uptake. Moreover, accumulation of diphenhydramine was stimulated by preloading the Caco-2 cells with these tertiary amines (trans-stimulation effect), indicating the existence of the specific transport system for tertiary amines with N-dimethyl or N-diethyl moieties. Efflux of diphenhydramine from monolayers was enhanced by medium acidification. In addition, intracellular acidification resulted in marked stimulation of diphenhydramine accumulation. ATP depletion of the cells caused an enhancement of diphenhydramine accumulation, suggesting the involvement of an active secretory pathway. However, P-glycoprotein did not mediate the diphenhydramine transport. These findings indicate that a novel pH-dependent tertiary amine transport system that recognizes N-dimethyl or N-diethyl moieties is involved in diphenhydramine transport in Caco-2 cells.
引用
收藏
页码:G563 / G569
页数:7
相关论文
共 34 条
[1]   EVIDENCE FOR A POLARIZED EFFLUX SYSTEM IN CACO-2 CELLS CAPABLE OF MODULATING CYCLOSPORINE-A TRANSPORT [J].
AUGUSTIJNS, PF ;
BRADSHAW, TP ;
GAN, LSL ;
HENDREN, RW ;
THAKKER, DR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (02) :360-365
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Fluoroquinolone (ciprofloxacin) secretion by human intestinal epithelial (Caco-2) cells [J].
Cavet, ME ;
West, M ;
Simmons, NL .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (08) :1567-1578
[4]   Direct demonstration of small intestinal secretion and site-dependent absorption of the beta-blocker talinolol in humans [J].
Gramatte, T ;
Oertel, R ;
Terhaag, B ;
Kirch, W .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 59 (05) :541-549
[5]   THE FUNCTION OF GP170, THE MULTIDRUG-RESISTANCE GENE-PRODUCT, IN THE BRUSH-BORDER OF RAT INTESTINAL-MUCOSA [J].
HSING, S ;
GATMAITAN, Z ;
ARIAS, IM .
GASTROENTEROLOGY, 1992, 102 (03) :879-885
[6]  
HUNTER J, 1993, J BIOL CHEM, V268, P14991
[7]   DRUG ABSORPTION LIMITED BY P-GLYCOPROTEIN-MEDIATED SECRETORY DRUG TRANSPORT IN HUMAN INTESTINAL EPITHELIAL CACO-2 CELL-LAYERS [J].
HUNTER, J ;
HIRST, BH ;
SIMMONS, NL .
PHARMACEUTICAL RESEARCH, 1993, 10 (05) :743-749
[8]  
INUI K, 1992, J PHARMACOL EXP THER, V261, P195
[9]  
Inui K, 1998, CLIN EXP NEPHROL, V2, P100
[10]  
Ito T, 1997, J PHARMACOL EXP THER, V282, P955