Update on the molecular physiology of organic anion transporters

被引:24
作者
Ahn, Sun-Young
Bhatnagar, Vibha [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Family & Prevent Med, VASDHCS, San Diego, CA 92161 USA
[2] VA San Diego Healthcare Syst, San Diego, VA USA
关键词
ischemia; nephrotoxicity; OAT; organic anion transporter; pharmacogenetics;
D O I
10.1097/MNH.0b013e32830b5d5d
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Organic anion transporters (OATs) mediate the renal absorption and excretion of a wide range of metabolites and xenobiotics. We discuss the recent advances that have been made in elucidating the binding and transport characteristics of OATs, new insights into their physiological role and regulation by various factors and, pharmacogenetics. Recent findings Overlapping substrate specificity among the OATs is well established. However, recent findings have suggested distinct differences in the structural binding determinants among the OATs which have important implications for understanding drug interactions and drug design. A potential role for OATs in blood pressure regulation and remote sensing has been reported. Meanwhile, factors regulating the expression of OATs continue to be identified and characterized. The effect of renal ischemia on OAT expression and function is currently being explored. Finally, recent studies identifying various OAT polymorphisms may facilitate prediction of individual drug response and toxicity. Summary As progress is made in unveiling the many functional aspects of the OATs, it is becoming clear that their significance is not only limited to a role in drug elimination from the body, but also extends to other vital physiological roles. Further delineation of the function and regulation of the OATs will uncover enormous potential clinical and pharmacological applications.
引用
收藏
页码:499 / 505
页数:7
相关论文
共 92 条
[61]   HNF1α controls renal glucose reabsorption in mouse and man [J].
Pontoglio, M ;
Prié, D ;
Cheret, C ;
Doyen, A ;
Leroy, C ;
Froguel, P ;
Velho, G ;
Yaniv, M ;
Friedlander, G .
EMBO REPORTS, 2000, 1 (04) :359-365
[62]  
Ranganathan P, 2008, J RHEUMATOL, V35, P572
[63]   Organic anion transporters of the SLC22 family: Biopharmaceutical, physiological, and pathological roles [J].
Rizwan, Ahsan N. ;
Burckhardt, Gerhard .
PHARMACEUTICAL RESEARCH, 2007, 24 (03) :450-470
[64]   Human renal organic anion transporters: Characteristics and contributions to drug and drug metabolite excretion [J].
Robertson, EE ;
Rankin, GO .
PHARMACOLOGY & THERAPEUTICS, 2006, 109 (03) :399-412
[65]   Molecular aspects of renal anionic drug transport [J].
Russel, FGM ;
Masereeuw, R ;
van Aubel, RAMH .
ANNUAL REVIEW OF PHYSIOLOGY, 2002, 64 :563-594
[66]   Transcriptional regulation of human and mouse organic anion transporter 1 by hepatocyte nuclear factor 1 α/β [J].
Saji, Takami ;
Kikuchi, Ryota ;
Kusuhara, Hiroyuki ;
Kim, Insook ;
Gonzalez, Frank J. ;
Sugiyama, Yuichi .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2008, 324 (02) :784-790
[67]   Downregulation of organic anion transporters OAT1 and OAT3 correlates with impaired secretion of para-aminohippurate after ischemic acute renal failure in rats [J].
Schneider, R. ;
Sauvant, C. ;
Betz, B. ;
Otremba, M. ;
Fischer, D. ;
Holzinger, H. ;
Wanner, C. ;
Galle, J. ;
Gekle, M. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2007, 292 (05) :F1599-F1605
[68]   Identification of multispecific organic anion transporter 2 expressed predominantly in the liver [J].
Sekine, T ;
Cha, SH ;
Tsuda, M ;
Apiwattanakul, N ;
Nakajima, N ;
Kanai, Y ;
Endou, H .
FEBS LETTERS, 1998, 429 (02) :179-182
[69]   Molecular physiology of renal organic anion transporters [J].
Sekine, T ;
Miyazaki, H ;
Endou, H .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2006, 290 (02) :F251-F261
[70]   Novel liver-specific organic anion transporter OAT7 that operates the exchange of sulfate conjugates for short chain fatty acid butyrate [J].
Shin, Ho Jung ;
Anzai, Naohiko ;
Enomoto, Atsushi ;
He, Xin ;
Kim, Do Kyung ;
Endou, Hitoshi ;
Kanai, Yoshikatsu .
HEPATOLOGY, 2007, 45 (04) :1046-1055