Molecular aspects of renal anionic drug transport

被引:184
作者
Russel, FGM [1 ]
Masereeuw, R [1 ]
van Aubel, RAMH [1 ]
机构
[1] Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Pharmacol & Toxicol, Nijmegen, Netherlands
关键词
drug excretion; organic anion transporter; multidrug resistance protein; organic anion transporting polypeptide;
D O I
10.1146/annurev.physiol.64.081501.155913
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Multiple organic anion transporters in the proximal tubule of the kidney are involved in the secretion of drugs, toxic compounds, and their metabolites. Many of these compounds are potentially hazardous on accumulation, and it is therefore not surprising that the proximal tubule is also an important target for toxicity. In the past few years, considerable progress has been made in the cloning of these transporters and their functional characterization following heterologous expression. Members of the organic anion transporter (OAT), organic anion transporting polypeptide (OATP), multidrug resistance protein (MRP), sodium-phosphate transporter (NPT), and peptide transporter (PEPT) families have been identified in the kidney. In this review, we summarize our current knowledge on their localization, molecular and functional characteristics, and substrate and inhibitor specificity. A major challenge for the future will be to understand how these transporters work in concert to accomplish the renal secretion of specific anionic substrates.
引用
收藏
页码:563 / 594
页数:34
相关论文
共 172 条
  • [1] Molecular characterization and tissue distribution of a new organic anion transporter subtype (oatp3) that transports thyroid hormones and taurocholate and comparison with oatp2
    Abe, T
    Kakyo, M
    Sakagami, H
    Tokui, T
    Nishio, T
    Tanemoto, M
    Nomura, H
    Hebert, SC
    Matsuno, S
    Kondo, H
    Yawo, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) : 22395 - 22401
  • [2] Apiwattanakul N, 1999, MOL PHARMACOL, V55, P847
  • [3] Genomic structure and in vivo expression of the human organic anion transporter 1 (hOAT1) gene
    Bahn, A
    Prawitt, D
    Buttler, D
    Reid, G
    Enklaar, T
    Wolff, NA
    Ebbinghaus, C
    Hillemann, A
    Schulten, HJ
    Gunawan, B
    Füzesi, L
    Zabel, B
    Burckhardt, G
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (02) : 623 - 630
  • [4] Interactions of the human multidrug resistance proteins MRP1 and MRP2 with organic anions
    Bakos, É
    Evers, R
    Sinkó, E
    Váradi, A
    Borst, P
    Sarkadi, B
    [J]. MOLECULAR PHARMACOLOGY, 2000, 57 (04) : 760 - 768
  • [5] Direct evidence for peptide transporter (PepT1)-mediated uptake of a nonpeptide prodrug, valacyclovir
    Balimane, PV
    Tamai, I
    Guo, AL
    Nakanishi, T
    Kitada, H
    Leibach, FH
    Tsuji, A
    Sinko, PJ
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (02) : 246 - 251
  • [6] Mutations in ABCC6 cause pseudoxanthoma elasticum
    Bergen, AAB
    Plomp, AS
    Schuurman, EJ
    Terry, S
    Breuning, M
    Dauwerse, H
    Swart, J
    Kool, M
    van Soest, S
    Baas, F
    ten Brink, JB
    de Jong, PTVM
    [J]. NATURE GENETICS, 2000, 25 (02) : 228 - 231
  • [7] Immunologic distribution of an organic anion transport protein in rat liver and kidney
    Bergwerk, AJ
    Shi, XY
    Ford, AC
    Kanai, N
    Jacquemin, E
    Burk, RD
    Bai, S
    Novikoff, PM
    Stieger, B
    Meier, PJ
    Schuster, VL
    Wolkoff, AW
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 271 (02): : G231 - G238
  • [8] Regulation of renal tubular secretion of organic compounds
    Berkhin, EB
    Humphreys, MH
    [J]. KIDNEY INTERNATIONAL, 2001, 59 (01) : 17 - 30
  • [9] BENEMID RHO-(DI-NORMAL-PROPYLSULFAMYL)-BENZOIC ACID - ITS RENAL AFFINITY AND ITS ELIMINATION
    BEYER, KH
    RUSSO, HF
    TILLSON, EK
    MILLER, AK
    VERWEY, WF
    GASS, SR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1951, 166 (03): : 625 - 640
  • [10] Inhibition of basolateral cAMP permeability in the toad urinary bladder
    Boom, A
    Golstein, PE
    Frérotte, M
    Van Sande, J
    Beauwens, R
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2000, 528 (01): : 189 - 198