Efflux transport systems for organic anions and cations at the blood-CSF barrier

被引:75
作者
Kusuhara, H [1 ]
Sugiyama, Y [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
关键词
efflux transport; organic anion; organic cation; OCT; OAT; OATP; MRP;
D O I
10.1016/j.addr.2004.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The choroid plexus (CP), located in the lateral, third and fourth ventricles, is the site of elimination of xenobiotics and endogenous waste from the cerebrospinal fluid (CSF) together with convective flow associated with CSF turnover. Active efflux transport systems, as well as metabolic enzymes in the choroid plexus epithelial cells (CPE), which form a tight rnonolayer. play a protective role by facilitating the elimination of xenobiotics including drugs and endogenous waste from the CSF to prevent their accumulation in the central nervous system. Except in the case of lipophilic cationic and neutral compounds, uptake and efflux transporters carry out the vectorial transport across the cell monolayer to transfer their common substrates efficiently from the CSF to the blood side. Many published studies have given us some insights into the uptake mechanisms for organic compounds at the brush border side of the CP. Organic anion transporters, such as Oatp3 and Oat3, play a major role in the uptake of amphipathic and hydrophilic organic anions, respectively, at the brush border surface of the CPE, while the organic cation transporters, Oct2 and/or Oct3, have been suggested to be involved in the uptake of hydrophilic organic cations. In contrast, the molecular characteristics of basolateral transporters have not been fully elucidated. Mrp1 is involved in the excretion of etoposide at the basolateral membrane of the CPE, but its contribution to the excretion of organic anions, especially amphipathic conjugated metabolites, remains controversial. The present manuscript summarizes the efflux transport mechanisms at the choroid plexus and focuses on the molecular characteristics of these transporters. (C) 2004 Published by Elsevier B.V.
引用
收藏
页码:1741 / 1763
页数:23
相关论文
共 159 条
[91]   In vitro study of the functional expression of organic anion transporting polypeptide 3 at rat choroid plexus epithelial cells and its involvement in the cerebrospinal fluid-to-blood transport of estrone-3-sulfate [J].
Ohtsuki, S ;
Takizawa, T ;
Takanaga, H ;
Terasaki, N ;
Kitazawa, T ;
Sasaki, M ;
Abe, T ;
Hosoya, KI ;
Terasaki, T .
MOLECULAR PHARMACOLOGY, 2003, 63 (03) :532-537
[92]   cDNA cloning and functional expression of a novel rat kidney organic cation transporter, OCT2 [J].
Okuda, M ;
Saito, H ;
Urakami, Y ;
Takano, M ;
Inui, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 224 (02) :500-507
[93]   Characterization of the transport properties of a quinolone antibiotic, fleroxacin, in rat choroid plexus [J].
Ooie, T ;
Suzuki, H ;
Terasaki, T ;
Sugiyama, Y .
PHARMACEUTICAL RESEARCH, 1996, 13 (04) :523-527
[94]   Identification of a novel human organic anion transporting polypeptide as a high affinity thyroxine transporter [J].
Pizzagalli, F ;
Hagenbuch, B ;
Stieger, B ;
Klenk, U ;
Folkers, G ;
Meier, PJ .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (10) :2283-2296
[95]   Mechanism of organic anion transport across the apical membrane of choroid plexus [J].
Pritchard, JB ;
Sweet, DH ;
Miller, DS ;
Walden, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) :33382-33387
[96]   Glutathione stimulates sulfated estrogen transport by multidrug resistance protein 1 [J].
Qian, YM ;
Song, WC ;
Cui, H ;
Cole, SPC ;
Deeley, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6404-6411
[97]   Choroid plexus epithelial expression of MDR1 P glycoprotein and multidrug resistance-associated protein contribute to the blood-cerebrospinal-fluid drug-permeability barrier [J].
Rao, VV ;
Dahlheimer, JL ;
Bardgett, ME ;
Snyder, AZ ;
Finch, RA ;
Sartorelli, AC ;
Piwnica-Worms, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3900-3905
[98]   Localization and function of the organic anion-transporting polypeptide Oatp2 in rat liver [J].
Reichel, C ;
Gao, B ;
Van Montfoort, J ;
Cattori, V ;
Rahner, C ;
Hagenbuch, B ;
Stieger, B ;
Kamisako, T ;
Meier, PJ .
GASTROENTEROLOGY, 1999, 117 (03) :688-695
[99]   The human multidrug resistance protein MRP4 functions as a prostaglandin efflux transporter and is inhibited by nonsteroidal antiinflammatory drugs [J].
Reid, G ;
Wielinga, P ;
Zelcer, N ;
van der Heijden, I ;
Kuil, A ;
de Haas, M ;
Wijnholds, J ;
Borst, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (16) :9244-9249
[100]   Molecular aspects of renal anionic drug transport [J].
Russel, FGM ;
Masereeuw, R ;
van Aubel, RAMH .
ANNUAL REVIEW OF PHYSIOLOGY, 2002, 64 :563-594