Decreased activity of basolateral organic ion transports in hyperuricemic rat kidney: roles of organic ion transporters, rOAT1 rOAT3 and rOCT2

被引:72
作者
Habu, Y
Yano, I
Takeuchi, A
Saito, H
Okuda, M
Fukatsu, A
Inui, K [1 ]
机构
[1] Kyoto Univ Hosp, Dept Pharm, Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ Hosp, Nephrol Sect Internal Med, Sakyo Ku, Kyoto 6068507, Japan
关键词
kidney; hyperuricemia; renal secretion; organic anion transporter; organic cation transporter;
D O I
10.1016/S0006-2952(03)00466-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated organic anion and cation transport activity and the expression of several organic ion transporters in hyperuricemic rat kidney. Feeding oxonic acid, an inhibitor of uric acid metabolism, and uric acid for 10 days significantly increased plasma uric acid level. Plasma creatinine and blood urea nitrogen concentrations also increased in hyperuricemic rats, indicating impaired renal function. The accumulation of organic anions, p-ammohippurate (PAH) and methotrexate, and cations, tetraethylammonium (TEA) and cimetidine, into renal slices was markedly decreased, suggesting decreased transport activity for organic anions and cations at the basolateral membrane in the kidney. The expression levels of basolateral organic anion transporters rOAT1 and rOAT3, and organic cation transporter, rOCT2, significantly decreased in hyperuricemic rat kidney as assessed by mRNA and protein levels. In contrast, the expression of rOCT1 was unaltered by hyperuricemia at both mRNA and protein levels. Moreover, the mRNA expression of kidney-specific organic anion transporters, OAT-K1 and OAT-K2, and organic anion transporting polypeptide (oatp) 1, which localize at the brush-border membrane in the kidney, was unchanged in hyperuricemic rats. In conclusion, we showed decreased basolateral organic anion and cation transport activity, accompanied by a specific decrease in rOAT1, rOAT3 and rOCT2 expression in hyperuricemic rat kidney. These phenomena partly contribute to the changed renal disposition of organic anions and cations in hyperuricemia. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1107 / 1114
页数:8
相关论文
共 36 条
[1]   RENAL-FUNCTION IN RATS WITH ACUTE MEDULLARY INJURY [J].
BROWN, EA ;
KLIGER, AS ;
HAYSLETT, JP ;
FINKELSTEIN, FO .
NEPHRON, 1980, 26 (02) :64-68
[2]   Electrogenic properties and substrate specificity of the polyspecific rat cation transporter rOCT1 [J].
Busch, AE ;
Quester, S ;
Ulzheimer, JC ;
Waldegger, S ;
Gorboulev, V ;
Arndt, P ;
Lang, F ;
Koepsell, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) :32599-32604
[3]   Identification and characterization of human organic anion transporter 3 expressing predominantly in the kidney [J].
Cha, SH ;
Sekine, T ;
Fukushima, J ;
Kanai, Y ;
Kobayashi, Y ;
Goya, T ;
Endou, H .
MOLECULAR PHARMACOLOGY, 2001, 59 (05) :1277-1286
[4]   Cisplatin induces renal expression of P-glycoprotein and canalicular multispecific organic anion transporter [J].
Demeule, M ;
Brossard, M ;
Béliveau, R .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (06) :F832-F840
[5]   DRUG EXCRETION MEDIATED BY A NEW PROTOTYPE OF POLYSPECIFIC TRANSPORTER [J].
GRUNDEMANN, D ;
GORBOULEV, V ;
GAMBARYAN, S ;
VEYHL, M ;
KOEPSELL, H .
NATURE, 1994, 372 (6506) :549-552
[6]   Assessment of cisplatin-induced nephrotoxicity by microarray technology [J].
Huang, Q ;
Dunn, RT ;
Jayadev, S ;
DiSorbo, O ;
Pack, FD ;
Farr, SB ;
Stoll, RE ;
Blanchard, KT .
TOXICOLOGICAL SCIENCES, 2001, 63 (02) :196-207
[7]   Cellular and molecular aspects of drug transport in the kidney [J].
Inui, K ;
Masuda, S ;
Saito, H .
KIDNEY INTERNATIONAL, 2000, 58 (03) :944-958
[8]  
Inui K, 1998, CLIN EXP NEPHROL, V2, P100
[9]   Significance of hyperuricemia on the early detection of renal failure in a cohort of screened subjects [J].
Iseki, K ;
Oshiro, S ;
Tozawa, M ;
Iseki, C ;
Ikemiya, Y ;
Takishita, S .
HYPERTENSION RESEARCH, 2001, 24 (06) :691-697
[10]   Distribution characteristics of levofloxacin and grepafloxacin in rat kidney [J].
Ito, T ;
Yano, I ;
Masuda, S ;
Hashimoto, Y ;
Inui, K .
PHARMACEUTICAL RESEARCH, 1999, 16 (04) :534-539