Molecular pharmacology of renal organic anion transporters

被引:140
作者
Van Aubel, RAMH [1 ]
Masereeuw, R [1 ]
Russel, FGM [1 ]
机构
[1] Univ Nijmegen, Dept Pharmacol & Toxicol 233, Inst Cellular Signaling, NL-6500 HB Nijmegen, Netherlands
关键词
multidrug resistance protein; peptide transporter; drug excretion; proximal tubule; kidney;
D O I
10.1152/ajprenal.2000.279.2.F216
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Renal organic anion transport systems play an important role in the elimination of drugs, toxic compounds, and their metabolites, many of which are potentially harmful to the body. The renal proximal tubule is the primary site of carrier-mediated transport from blood to urine of a wide variety of anionic substrates. Recent studies have shown that organic anion secretion in renal proximal tubule is mediated by distinct sodium-dependent and sodium-independent transport systems. Knowledge of the molecular identity of these transporters and their substrate specificity has increased considerably in the past few years by cloning of various carrier proteins. However, a number of fundamental questions still have to be answered to elucidate the participation of the cloned transporters in the overall tubular secretion of anionic xenobiotics. This review summarizes the latest knowledge on molecular and pharmacological properties of renal organic anion transporters and homologs, with special reference to their nephron and plasma membrane localization, transport characteristics, and substrate and inhibitor specificity. A number of the recently cloned transporters, such as the p-aminohippurate/dicarboxylate exchanger OAT1, the anion/sulfate exchanger SAT1, the peptide transporters PEPT1 and PEPT2, and the nucleoside transporters CNT1 and CNT2, are key proteins in organic anion handling that possess the same characteristics as has been predicted from previous physiological studies. The role of other cloned transporters, such as MRP1, MRP2, OATP1, OAT-K1, and OAT-K2, is still poorly characterized, whereas the only information that is available on the homologs OAT2, OAT3, OATP3, and MRP3-6 is that they are expressed in the kidney, but their localization, not to mention their function, remains to be elucidated.
引用
收藏
页码:F216 / F232
页数:17
相关论文
共 204 条
[51]  
HUANG QQ, 1994, J BIOL CHEM, V269, P17757
[52]   SPECIFICITY OF A PARTICULATE RAT RENAL PEPTIDASE AND ITS LOCALIZATION ALONG WITH OTHER ENZYMES OF MERCAPTURIC ACID SYNTHESIS [J].
HUGHEY, RP ;
RANKIN, BB ;
ELCE, JS ;
CURTHOYS, NP .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 186 (02) :211-217
[53]   DIFFERENTIAL LOCALIZATION OF UDP-GLUCURONOSYLTRANSFERASE IN KIDNEY DURING HUMAN EMBRYONIC AND FETAL DEVELOPMENT [J].
HUME, R ;
COUGHTRIE, MWH ;
BURCHELL, B .
ARCHIVES OF TOXICOLOGY, 1995, 69 (04) :242-247
[54]  
ISHIKAWA T, 1990, J BIOL CHEM, V265, P19279
[55]  
Ishizuka H, 1997, J PHARMACOL EXP THER, V280, P1304
[56]  
Ishizuka H, 1998, J PHARMACOL EXP THER, V287, P37
[57]   Molecular cloning of canalicular multispecific organic anion transporter defective in EHBR [J].
Ito, K ;
Suzuki, H ;
Hirohashi, T ;
Kume, K ;
Shimizu, T ;
Sugiyama, Y .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (01) :G16-G22
[58]   Functional analysis of a canalicular multispecific organic anion transporter cloned from rat liver [J].
Ito, K ;
Suzuki, H ;
Hirohashi, T ;
Kume, K ;
Shimizu, T ;
Sugiyama, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) :1684-1688
[59]   EXPRESSION CLONING OF A RAT-LIVER NA+-INDEPENDENT ORGANIC ANION TRANSPORTER [J].
JACQUEMIN, E ;
HAGENBUCH, B ;
STIEGER, B ;
WOLKOFF, AW ;
MEIER, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (01) :133-137
[60]  
Jedlitschky G, 1996, CANCER RES, V56, P988