Expression levels of renal organic anion transporters (OATs) and their correlation with anionic drug excretion in patients with renal diseases

被引:97
作者
Sakurai, Y
Motohashi, H
Ueo, H
Masuda, S
Saito, H
Okuda, M
Mori, N
Matsuura, M
Doi, T
Fukatsu, A
Ogawa, O
Inui, K [1 ]
机构
[1] Kyoto Univ, Fac Med, Kyoto Univ Hosp, Dept Pharm,Sakyo Ku, Kyoto 6068507, Japan
[2] Shizuoka Prefectural Hosp, Dept Nephrol, Shizuoka, Japan
[3] Univ Tokushima, Dept Clin Biol & Med, Tokushima 770, Japan
[4] Kyoto Univ, Fac Med, Kyoto Univ Hosp, Div Artificial Kidneys,Sakyo Ku, Kyoto 6068507, Japan
[5] Kyoto Univ, Fac Med, Kyoto Univ Hosp, Dept Urol,Sakyo Ku, Kyoto 6068507, Japan
关键词
organic anion transporter; renal diseases; human kidney; renal tubular secretion; real-time PCR;
D O I
10.1023/B:PHAM.0000012153.71993.cb
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Purpose. Because the urinary excretion of drugs is often decreased in renal diseases, dosage regimens are adjusted to avoid adverse drug reactions. The aim of present study was to clarify the alteration in the levels of renal drug transporters and their correlation with the urinary drug excretion in renal diseases patients. Methods. We quantified the mRNA levels of human organic anion transporters (hOATs) by real-time polymerase chain reaction and examined the excretion of the anionic drug, cefazolin, in renal disease patients. Moreover, transport of cefazolin by hOAT1 and hOAT3 were examined using HEK293 transfectants. Results. Among four hOATs, the level of hOAT1 mRNA was significantly lower in the kidney of patients with renal diseases than in the normal controls. The elimination constant of cefazolin showed a significant correlation with the values of phenolsulfonphthalein test and mRNA levels of hOAT3. The uptake study using HEK293 transfectants revealed that cefazolin and phenolsulfonphthalein were transported by hOAT3. Conclusions. These results suggest that hOAT3 plays an important role for anionic drug secretion in patients with renal diseases and that the expression levels of drug transporters may be related to the alteration of renal drug secretion.
引用
收藏
页码:61 / 67
页数:7
相关论文
共 30 条
[1]
Role of human organic anion transporter 4 in the transport of ochratoxin A [J].
Babu, E ;
Takeda, M ;
Narikawa, S ;
Kobayashi, Y ;
Enomoto, A ;
Tojo, A ;
Cha, SH ;
Sekine, T ;
Sakthisekaran, D ;
Endou, H .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2002, 1590 (1-3) :64-75
[2]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]
KIDNEY TRANSPORT OF CEFAZOLIN IN NORMAL AND IMPAIRED RENAL-FUNCTION [J].
BRODWALL, EK ;
BERGAN, T ;
ORJAVIK, O .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1977, 3 (06) :585-592
[4]
Enabling educational collaboration - a new shared reality [J].
Brown, JR .
COMPUTERS & GRAPHICS-UK, 2000, 24 (02) :289-292
[5]
Structure of renal organic anion and cation transporters [J].
Burckhardt, G ;
Wolff, NA .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (06) :F853-F866
[6]
FUROSEMIDE EFFECT ON ISOLATED PERFUSED TUBULES [J].
BURG, M ;
STONER, L ;
CARDINAL, J ;
GREEN, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1973, 225 (01) :119-124
[7]
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
[8]
DETTLI L, 1976, Clinical Pharmacokinetics, V1, P126, DOI 10.2165/00003088-197601020-00004
[9]
Interaction of human organic anion transporters 2 and 4 with organic anion transport inhibitors [J].
Enomoto, A ;
Takeda, M ;
Shimoda, M ;
Narikawa, S ;
Kobayashi, Y ;
Kobayashi, Y ;
Yamamoto, T ;
Sekine, T ;
Cha, SH ;
Niwa, T ;
Endou, H .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 301 (03) :797-802
[10]
A NEW DOSING REGIMEN IN RENAL-INSUFFICIENCY - APPLICATION TO CEPHALEXIN [J].
HORI, R ;
OKUMURA, K ;
NIHIRA, H ;
NAKANO, H ;
AKAGI, K ;
KAMIYA, A .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1985, 38 (03) :290-295