Modulation of drug transporters at the blood-brain barrier

被引:74
作者
Fricker, G
Miller, DS
机构
[1] Heidelberg Univ, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
[2] NIEHS, Lab Pharmacol & Chem, NIH, Res Triangle Pk, NC 27709 USA
关键词
ABC proteins; active transport; blood brain barrier; membrane carrier proteins; Mrp; P-glycoprotein; immunoliposomes; nanoparticles; drug targeting; Oat; Oatp;
D O I
10.1159/000075545
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A major challenge in the management of diseases of the central nervous system is the limited penetration of drugs into the brain. The structures responsible are the capillaries of the brain, whose endothelial cells form the so-called blood-brain barrier. Understanding the cellular and molecular structure as well as integrated function of this barrier is a prerequisite for successful drug delivery to the brain. Here we briefly review current knowledge about the active transport proteins (ABC and organic anion transporters) which function at the blood-brain barrier. We describe novel approaches to (1) modulate carrier protein function, and (2) circumvent the transporter-based carrier by targeted site-specific drug delivery systems, such as immunoliposome and nanoparticulate systems. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:169 / 176
页数:8
相关论文
共 61 条
[1]   Aluminum citrate is transported from brain into blood via the monocarboxylic acid transporter located at the blood-brain barrier [J].
Ackley, DC ;
Yokel, RA .
TOXICOLOGY, 1997, 120 (02) :89-97
[2]   Blood-brain barrier is involved in the efflux transport of a neuroactive steroid, dehydroepiandrosterone sulfate, via organic anion transporting polypeptide 2 [J].
Asaba, H ;
Hosoya, K ;
Takanaga, H ;
Ohtsuki, S ;
Tamura, E ;
Takizawa, T ;
Terasaki, T .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (05) :1907-1916
[3]  
Batrakova EV, 2001, J PHARMACOL EXP THER, V296, P551
[4]   P-glycoprotein is strongly expressed in the luminal membranes of the endothelium of blood vessels in the brain [J].
Beaulieu, E ;
Demeule, M ;
Ghitescu, L ;
Beliveau, R .
BIOCHEMICAL JOURNAL, 1997, 326 :539-544
[5]   Morphological and cytochemical aspects of capillary permeability [J].
Bendayan, M .
MICROSCOPY RESEARCH AND TECHNIQUE, 2002, 57 (05) :327-349
[6]   Endocytosis and transcytosis of an immunoliposome-based brain drug delivery system [J].
Cerletti, A ;
Drewe, J ;
Fricker, G ;
Eberle, AN ;
Huwyler, J .
JOURNAL OF DRUG TARGETING, 2000, 8 (06) :435-+
[7]   Localisation of breast cancer resistance protein in microvessel endothelium of human brain [J].
Cooray, HC ;
Blackmore, CG ;
Maskell, L ;
Barrand, MA .
NEUROREPORT, 2002, 13 (16) :2059-2063
[8]   MULTIDRUG-RESISTANCE GENE (P-GLYCOPROTEIN) IS EXPRESSED BY ENDOTHELIAL-CELLS AT BLOOD-BRAIN BARRIER SITES [J].
CORDONCARDO, C ;
OBRIEN, JP ;
CASALS, D ;
RITTMANGRAUER, L ;
BIEDLER, JL ;
MELAMED, MR ;
BERTINO, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) :695-698
[9]  
DAGENIS C, 2000, J PHARMACOL EXP THER, V294, P73
[10]  
Deguchi Y, 1997, J PHARMACOL EXP THER, V280, P551