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
[1]   Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1 [J].
Abe, T ;
Kakyo, M ;
Tokui, T ;
Nakagomi, R ;
Nishio, T ;
Nakai, D ;
Nomura, H ;
Unno, M ;
Suzuki, M ;
Naitoh, T ;
Matsuno, S ;
Yawo, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (24) :17159-17163
[2]   Molecular characterization and tissue distribution of a new organic anion transporter subtype (oatp3) that transports thyroid hormones and taurocholate and comparison with oatp2 [J].
Abe, T ;
Kakyo, M ;
Sakagami, H ;
Tokui, T ;
Nishio, T ;
Tanemoto, M ;
Nomura, H ;
Hebert, SC ;
Matsuno, S ;
Kondo, H ;
Yawo, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22395-22401
[3]   Expression of human organic anion transporters in the choroid plexus and their interactions with neurotransmitter metabolites [J].
Alebouyeh, M ;
Takeda, M ;
Onozato, ML ;
Tojo, A ;
Noshiro, R ;
Hasannejad, H ;
Inatomi, J ;
Narikawa, S ;
Huang, XL ;
Khamdang, S ;
Anzai, N ;
Endou, H .
JOURNAL OF PHARMACOLOGICAL SCIENCES, 2003, 93 (04) :430-436
[4]   The choroid plexus epithelium is the site of the organic anion transport protein in the brain [J].
Angeletti, RH ;
Novikoff, PM ;
Juvvadi, SR ;
Fritschy, JM ;
Meier, PJ ;
Wolkoff, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (01) :283-286
[5]   Human organic anion transporter 3 (hOAT3) can operate as an exchanger and mediate secretory urate flux [J].
Bakhiya, N ;
Bahn, A ;
Burckhardt, G ;
Wolff, NA .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2003, 13 (05) :249-256
[6]   Expression cloning and functional characterization of the kidney cortex high-affinity proton-coupled peptide transporter [J].
Boll, M ;
Herget, M ;
Wagener, M ;
Weber, WM ;
Markovich, D ;
Biber, J ;
Clauss, W ;
Murer, H ;
Daniel, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :284-289
[7]   A family of drug transporters: The multidrug resistance-associated proteins [J].
Borst, P ;
Evers, R ;
Kool, M ;
Wijnholds, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (16) :1295-1302
[8]   Multispecific amphipathic substrate transport by an organic anion transporter of human liver [J].
Bossuyt, X ;
Muller, M ;
Meier, PJ .
JOURNAL OF HEPATOLOGY, 1996, 25 (05) :733-738
[9]   Confocal imaging of organic anion transport in intact rat choroid plexus [J].
Breen, CM ;
Sykes, DB ;
Fricker, G ;
Miller, DS .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2002, 282 (05) :F877-F885
[10]   Molecular characterization of the renal organic anion transporter 1 [J].
Burckhardt, G ;
Wolff, NA ;
Bahn, A .
CELL BIOCHEMISTRY AND BIOPHYSICS, 2002, 36 (2-3) :169-174