Efflux transport systems for drugs at the blood-brain barrier and blood-cerebrospinal fluid barrier (Part 1)

被引:132
作者
Kusuhara, H [1 ]
Sugiyama, Y [1 ]
机构
[1] Univ Tokyo, Fac Pharmaceut Sci, Dept Biopharmaceut, Tokyo 113, Japan
关键词
D O I
10.1016/S1359-6446(00)01632-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Penetration through the blood-brain barrier (BBB) and blood-cerebrospinal fluid barrier (BCSF B) is necessary if a drug is to achieve the required concentration for a desired pharmacological effect. Efflux transport systems at the BBB and BCSFB provide a protective barrier function by removing drugs from the brain or cerebrospinal fluid and transferring them to the systemic circulation, respectively; several transporters at the BBB and BCSFB have been identified. Efflux transport should be taken into consideration during drug development to improve brain penetration and to avoid drug-drug interactions involving these transporters and subsequent side effects.
引用
收藏
页码:150 / 156
页数:7
相关论文
共 56 条
[1]   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
[2]   SATURABLE EFFLUX OF THE PEPTIDES RC-160 AND TYR-MIF-1 BY DIFFERENT PARTS OF THE BLOOD-BRAIN-BARRIER [J].
BANKS, WA ;
KASTIN, AJ ;
SAM, HM ;
CAO, VT ;
KING, B ;
MANESS, LM ;
SCHALLY, AV .
BRAIN RESEARCH BULLETIN, 1994, 35 (02) :179-182
[3]   Structure of renal organic anion and cation transporters [J].
Burckhardt, G ;
Wolff, NA .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (06) :F853-F866
[4]   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
[5]   Development of an in situ mouse brain perfusion model and its application to mdr1a P-glycoprotein-deficient mice [J].
Dagenais, C ;
Rousselle, C ;
Pollack, GM ;
Scherrmann, JM .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (02) :381-386
[6]   HEPATOBILIARY SECRETION OF ORGANIC-COMPOUNDS - MOLECULAR MECHANISMS OF MEMBRANE-TRANSPORT [J].
ELFERINK, RPJO ;
MEIJER, DKF ;
KUIPERS, F ;
JANSEN, PLM ;
GROEN, AK ;
GROOTHUIS, GMM .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON BIOMEMBRANES, 1995, 1241 (02) :215-268
[7]  
Gao B, 2000, J PHARMACOL EXP THER, V294, P73
[8]   Localization of the organic anion transporting polypeptide 2 (Oatp2) in capillary endothelium and choroid plexus epithelium of rat brain [J].
Gao, P ;
Stieger, B ;
Noé, B ;
Fritschy, JM ;
Meier, PJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1999, 47 (10) :1255-1263
[9]   Expression of multidrug resistance-associated protein (MRP) in brain microvessel endothelial cells [J].
Han, HY ;
Secrest, DT ;
Mark, KS ;
Carney, D ;
Brandquist, C ;
Elmquist, WF ;
Miller, DW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 243 (03) :816-820
[10]   99mTc-sestamibi is a substrate for P-glycoprotein and the multidrug resistance-associated protein [J].
Hendrikse, NH ;
Franssen, EJF ;
van der Graaf, WTA ;
Meijer, C ;
Piers, DA ;
Vaalburg, W ;
de Vries, EGE .
BRITISH JOURNAL OF CANCER, 1998, 77 (03) :353-358