Fruit Juices as Perpetrators of Drug Interactions: The Role of Organic Anion-Transporting Polypeptides

被引:53
作者
Dolton, M. J. [1 ]
Roufogalis, B. D. [1 ]
McLachlan, A. J. [1 ,2 ]
机构
[1] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
[2] Concord Repatriat Gen Hosp, Ctr Educ & Res Ageing, Concord, Australia
关键词
EFFECTIVE RENIN INHIBITOR; MESSENGER-RNA EXPRESSION; FORTIFIED ORANGE JUICE; HUMAN INTESTINAL-TRACT; GRAPEFRUIT JUICE; P-GLYCOPROTEIN; PLASMA-CONCENTRATIONS; OATP-B; CACO-2; CELLS; APPLE JUICE;
D O I
10.1038/clpt.2012.159
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Grapefruit juice is widely recognized to cause important drug interactions via inhibition of CYP3A4, and a wider variety of fruit juices have been shown to inhibit influx transporters in enterocytes known as organic anion-transporting polypeptides (OATPs). Fruit juice coadministration significantly reduces the oral bioavailability of numerous important medicines relying on this anion transporter pathway for absorption. This article reviews the current literature on interactions between clinically used OATP substrates and fruit juice consumption.
引用
收藏
页码:622 / 630
页数:9
相关论文
共 76 条
[1]
A comparison of selected mRNA and protein abundances in human liver [J].
Anderson, L ;
Seilhamer, J .
ELECTROPHORESIS, 1997, 18 (3-4) :533-537
[2]
Effects of grapefruit juice on the pharmacokinetics of pitavastatin and atorvastatin [J].
Ando, H ;
Tsuruoka, S ;
Yanagihara, H ;
Sugimoto, K ;
Miyata, M ;
Yamazoe, Y ;
Takamura, T ;
Kaneko, S ;
Fujimura, A .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 60 (05) :494-497
[3]
Naringin is a major and selective clinical inhibitor of organic anion-transporting polypeptide 1A2 (OATP1A2) in grapefruit juice [J].
Bailey, D. G. ;
Dresser, G. K. ;
Leake, B. F. ;
Kim, R. B. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 81 (04) :495-502
[4]
BAILEY DG, 1989, CLIN INVEST MED, V12, P357
[5]
Expression of transporters potentially involved in the targeting of cytostatic bile acid derivatives to colon cancer and polyps [J].
Ballestero, Maria R. ;
Monte, Maria J. ;
Briz, Oscar ;
Jimenez, Felipe ;
Martin, Francisco Gonzalez-San ;
Marin, Jose J. G. .
BIOCHEMICAL PHARMACOLOGY, 2006, 72 (06) :729-738
[6]
Grapefruit juice reduces the oral bioavailability of fexofenadine but not desloratadine [J].
Banfield, C ;
Gupta, S ;
Marino, M ;
Lim, J ;
Affrime, M .
CLINICAL PHARMACOKINETICS, 2002, 41 (04) :311-318
[7]
Variation of flavonoids and furanocoumarins in grapefruit juices: A potential source of variability in grapefruit juice-drug interaction studies [J].
De Castro, WV ;
Mertens-Talcott, S ;
Rubner, A ;
Butterweck, V ;
Derendorf, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (01) :249-255
[8]
Effect of grapefruit juice volume on the reduction of fexofenadine bioavailability: Possible role of organic anion transporting polypeptides [J].
Dresser, GK ;
Kim, RB ;
Bailey, DG .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 77 (03) :170-177
[9]
Fruit juices inhibit organic anion transporting polypeptide-mediated drug uptake to decrease the oral availability of fexofenadine [J].
Dresser, GK ;
Bailey, DG ;
Leake, BF ;
Schwarz, UI ;
Dawson, PA ;
Freeman, DJ ;
Kim, RB .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2002, 71 (01) :11-20
[10]
6′,7′-Dihydroxybergamottin in grapefruit juice and Seville orange juice:: Effects on cyclosporine disposition, enterocyte CYP3A4, and P-glycoprotein [J].
Edwards, DJ ;
Fitzsimmons, ME ;
Schuetz, EG ;
Yasuda, K ;
Ducharme, MP ;
Warbasse, LH ;
Woster, PM ;
Schuetz, JD ;
Watkins, P .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 65 (03) :237-244