Expression and Regulation of Drug Transporters and Metabolizing Enzymes in the Human Gastrointestinal Tract

被引:20
作者
Drozdzik, M. [1 ]
Oswald, S. [2 ]
机构
[1] Pomeranian Med Univ, Dept Pharmacol, Powstancow Wlkp 72, PL-70111 Szczecin, Poland
[2] Ernst Moritz Arndt Univ Greifswald, Dept Clin Pharmacol, Greifswald, Germany
关键词
Drug metabolizing enzymes; drug transporters; gastrointestinal tract; MESSENGER-RNA EXPRESSION; CANCER RESISTANCE PROTEIN; INFLAMMATORY-BOWEL-DISEASE; P-GLYCOPROTEIN EXPRESSION; HUMAN INTESTINAL-TRACT; UDP-GLUCURONOSYLTRANSFERASE ACTIVITY; SOLUTE-CARRIER TRANSPORTERS; MULTIDRUG-RESISTANCE; CELL-LINES; ULCERATIVE-COLITIS;
D O I
10.2174/0929867323666161024154457
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Orally administered drugs must pass through the intestinal wall and then through the liver before reaching systemic circulation. During this process drugs are subjected to different processes that may determine the therapeutic value. The intestinal barrier with active drug metabolizing enzymes and drug transporters in enterocytes plays an important role in the determination of drug bioavailability. Accumulating information demonstrates variable distribution of drug metabolizing enzymes and transporters along the human gastrointestinal tract (GI), that creates specific barrier characteristics in different segments of the GI. In this review, expression of drug metabolizing enzymes and transporters in the healthy and diseased human GI as well as their regulatory aspects: genetic, miRNA, DNA methylation are outlined. The knowledge of unique interplay between drug metabolizing enzymes and transporters in specific segments of the GI tract allows more precise definition of drug release sites within the GI in order to assure more complete bioavailability and prediction of drug interactions.
引用
收藏
页码:4468 / 4489
页数:22
相关论文
共 113 条
[1]   A LOW PLATELET COUNT IS ASSOCIATED WITH TREATMENT FAILUREIN PRETERM INFANTS TREATED WITH IBUPROFEN FOR PATENT DUCTUS ARTERIOSUS (PDA) [J].
Schena, F. ;
Ciarmoli, E. ;
Ghirardello, S. ;
Groppo, M. ;
Lonati, A. ;
Mosca, F. .
PEDIATRIC RESEARCH, 2010, 68 :118-119
[2]   Genetic variants of the human dipeptide transporter PEPT1 [J].
Anderle, P ;
Nielsen, CU ;
Pinsonneault, J ;
Krog, PL ;
Brodin, B ;
Sadée, W .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 316 (02) :636-646
[3]  
[Anonymous], 2012, AVAILABILITY FED REG
[4]   Gene and protein expression of P-glycoprotein, MRP1, MRP2, and CYP3A4 in the small and large human intestine [J].
Berggren, Sofia ;
Gall, Christine ;
Wollnitz, Nadine ;
Ekelund, Mats ;
Karlbom, Urban ;
Hoogstraate, Janet ;
Schrenk, Dieter ;
Lennernas, Hans .
MOLECULAR PHARMACEUTICS, 2007, 4 (02) :252-257
[5]  
Bergheim Ina, 2005, BMC Clin Pharmacol, V5, P4, DOI 10.1186/1472-6904-5-4
[6]   Gene Expression Profiling of Systems Involved in the Metabolism and the Disposition of Xenobiotics: Comparison between Human Intestinal Biopsy Samples and Colon Cell Lines [J].
Bourgine, Joanna ;
Billaut-Laden, Ingrid ;
Happillon, Melanie ;
Lo-Guidice, Jean-Marc ;
Maunoury, Vincent ;
Imbenotte, Michel ;
Broly, Franck .
DRUG METABOLISM AND DISPOSITION, 2012, 40 (04) :694-705
[7]   Phase II Metabolism of Hesperetin by Individual UDP-Glucuronosyltransferases and Sulfotransferases and Rat and Human Tissue Samples [J].
Brand, Walter ;
Boersma, Marelle G. ;
Bik, Hanneke ;
Hoek-van den Hil, Elisabeth F. ;
Vervoort, Jacques ;
Barron, Denis ;
Meinl, Walter ;
Glatt, Hansruedi ;
Williamson, Gary ;
van Bladeren, Peter J. ;
Rietjens, Ivonne M. C. M. .
DRUG METABOLISM AND DISPOSITION, 2010, 38 (04) :617-625
[8]   Expression of CYP3A isoforms and P-glycoprotein in human stomach, jejunum and ileum [J].
Canaparo, Roberto ;
Finnstrom, Niklas ;
Serpe, Loredana ;
Nordmark, Anna ;
Muntoni, Elisabetta ;
Eandi, Mario ;
Rane, Anders ;
Zara, Gian Paolo .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2007, 34 (11) :1138-1144
[9]  
Cascorbi I, 2011, HANDB EXP PHARMACOL, V201, P261, DOI 10.1007/978-3-642-14541-4_6
[10]   Proximal Roux-en-Y Gastric Bypass Alters Drug Absorption Pattern But Not Systemic Exposure of CYP3A4 and P-glycoprotein Substrates [J].
Chan, Lingtak-Neander ;
Lin, Yvonne S. ;
Tay-Sontheimer, Jessica C. ;
Trawick, Dorothy ;
Oelschlager, Brant K. ;
Flum, David R. ;
Patton, Kristen K. ;
Shen, Danny D. ;
Horn, John R. .
PHARMACOTHERAPY, 2015, 35 (04) :361-369