Barrier mechanisms in the brain, I. Adult brain

被引:132
作者
Saunders, NR [1 ]
Habgood, MD [1 ]
Dziegielewska, KM [1 ]
机构
[1] Univ Tasmania, Hobart, Tas 7001, Australia
关键词
blood-brain barrier; brain vessel permeability; cerebral endothelium; cerebrospinal fluid; choroid plexus; drug delivery; drug permeability; P-glycoprotein; sink effect; tight junctions;
D O I
10.1046/j.1440-1681.1999.02986.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The adult brain functions within a well-controlled (internal) environment that is separate from that of the internal environment of the rest of the body as a whole. 2. The underlying mechanism of control of the brain's internal environment lies in the presence of tight junctions between the cerebral endothelial cells at the blood-brain interface (blood-brain barrier) and between choroid plexus epithelial cells (blood-cerebrospinal fluid (CSF) barrier). 3. The effect of tight junctions at the blood-brain and blood-CSF barriers is to convert the properties of the individual endothelial and epithelial cells into properties of these interfaces as a whole. 4. Superimposed on the diffusion restriction provided by the tight junctions in the blood-brain and blood-CSF barriers is a series of transport mechanisms into and out of the brain and CSF that determine and control the internal environment of the brain with respect to a wide range of molecules, such as electrolytes, amino acids, glucose, vitamins and peptides, 5. The physical characteristics of drugs, together with their interaction with the properties of the barriers between blood, brain and CSF, determine the extent to which drugs penetrate into the brain. 6. Drugs can be targeted to the brain by making use of knowledge of this interaction between the physical properties of a drug (which can be modified by manipulation of the structure of the molecule in predictable ways) and the influx/efflux mechanisms present in the blood-CSF and blood-brain interfaces.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 80 条
[51]  
NEUWELT EA, 1989, IMPLICATIONS BLOOD B, V2
[52]   BRAIN EXTRACELLULAR SPACE AND SINK ACTION OF CEREBROSPINAL FLUID - MEASUREMENT OF RABBIT BRAIN EXTRACELLULAR SPACE USING SUCROSE LABELED WITH CARBON 14 [J].
OLDENDORF, WH ;
DAVSON, H .
ARCHIVES OF NEUROLOGY, 1967, 17 (02) :196-+
[53]   VECTOR-MEDIATED PEPTIDE DRUG-DELIVERY TO THE BRAIN [J].
PARDRIDGE, WM .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 15 (1-3) :109-146
[54]   Drug delivery to the brain [J].
Pardridge, WM .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (07) :713-731
[55]   VECTOR-MEDIATED DELIVERY OF A POLYAMIDE (PEPTIDE) NUCLEIC-ACID ANALOG THROUGH THE BLOOD-BRAIN-BARRIER IN-VIVO [J].
PARDRIDGE, WM ;
BOADO, RJ ;
KANG, YS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5592-5596
[56]  
Pardridge WM, 1993, DRUG DELIV, V1, P83
[57]   SYSTEMIC TOXIC EFFECTS ASSOCIATED WITH HIGH-DOSE VERAPAMIL INFUSION AND CHEMOTHERAPY ADMINISTRATION [J].
PENNOCK, GD ;
DALTON, WS ;
ROESKE, WR ;
APPLETON, CP ;
MOSLEY, K ;
PLEZIA, P ;
MILLER, TP ;
SALMON, SE .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (02) :105-110
[58]   PASSAGE OF CERTAIN SUBSTANCES OUT OF CEREBROSPINAL FLUID [J].
POLLAY, M ;
DAVSON, H .
BRAIN, 1963, 86 (01) :137-&
[59]   TIGHT-JUNCTIONAL MODIFICATION AS THE BASIS OF OSMOTIC OPENING OF THE BLOOD-BRAIN-BARRIER [J].
RAPOPORT, SI ;
ROBINSON, PJ .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 481 :250-267
[60]   DRUG ENTRY INTO THE BRAIN [J].
RAPOPORT, SI ;
OHNO, K ;
PETTIGREW, KD .
BRAIN RESEARCH, 1979, 172 (02) :354-359