Brain barrier systems: a new frontier in metal neurotoxicological research

被引:381
作者
Zheng, W
Aschner, M
Ghersi-Egea, JF
机构
[1] Purdue Univ, Sch Hlth Sci, W Lafayette, IN 47907 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27103 USA
[3] Fac Med Laennec, INSERM, Lyon, France
关键词
blood-brain barrier; blood-CSF barrier; choroid plexus; astrocytes; iron; lead; mercury; manganese; neurotoxicology; toxicant; transport;
D O I
10.1016/S0041-008X(03)00251-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The concept of brain barriers or a brain barrier system embraces the blood-brain interface, referred to as the blood-brain barrier, and the blood-cerebrospinal fluid (CSF) interface, referred to as the blood-CSF barrier. These brain barriers protect the CNS against chemical insults, by different complementary mechanisms. Toxic metal molecules can either bypass these mechanisms or be sequestered in and therefore potentially deleterious to brain barriers. Supportive evidence suggests that damage to blood-brain interfaces can lead to chemical-induced neurotoxicities. This review article examines the unique structure, specialization, and function of the brain barrier system, with particular emphasis on its toxicological implications. Typical examples of metal transport and toxicity at the barriers, such as lead (Pb), mercury (Hg), iron (Fe), and manganese (Mn), are discussed in detail with a special focus on the relevance to their toxic neurological consequences. Based on these discussions, the emerging research needs, such as construction of the new concept of blood-brain regional barriers, understanding of chemical effect on aged or immature barriers, and elucidation of the susceptibility of tight junctions to toxicants, are identified and addressed in this newly evolving field of neurotoxicology. They represent both clear challenges and fruitful research domains not only in neurotoxicology, but also in neurophysiology and pharmacology. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:1 / 11
页数:11
相关论文
共 98 条
[61]   An in vitro study of m-dinitrobenzene toxicity on the cellular components of the blood-brain barrier, astrocytes and endothelial cells [J].
Romero, IA ;
Ray, DE ;
Chan, MWK ;
Abbott, NJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 139 (01) :94-101
[62]   The cell biology of the blood-brain barrier [J].
Rubin, LL ;
Staddon, JM .
ANNUAL REVIEW OF NEUROSCIENCE, 1999, 22 :11-28
[63]   P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs [J].
Schinkel, AH ;
Wagenaar, E ;
Mol, CAAM ;
vanDeemter, L .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (11) :2517-2524
[64]  
Schreiber G, 2001, MICROSC RES TECHNIQ, V52, P21, DOI 10.1002/1097-0029(20010101)52:1<21::AID-JEMT4>3.0.CO
[65]  
2-Z
[66]  
SelvinTesta A, 1997, NEUROTOXICOLOGY, V18, P805
[67]   ELECTRON-PROBE MICROANALYSIS OF ISOLATED BRAIN CAPILLARIES POISONED WITH LEAD [J].
SILBERGELD, EK ;
WOLINSKY, JS ;
GOLDSTEIN, GW .
BRAIN RESEARCH, 1980, 189 (02) :369-376
[68]   LEAD TRANSPORT AND BINDING BY HUMAN ERYTHROCYTES INVITRO [J].
SIMONS, TJB .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 423 (3-4) :307-313
[69]   STUDIES IN CEREBRAL OEDEMA AND CEREBRAL SWELLING .1. THE CHANGES IN LEAD ENCEPHALOPATHY IN CHILDREN COMPARED WITH THOSE IN ALKYL TIN POISONING IN ANIMALS [J].
SMITH, JF ;
MCLAURIN, RL ;
NICHOLS, JB ;
ASBURY, A .
BRAIN, 1960, 83 (03) :411-&
[70]  
Smith Q., 1997, Metals and Oxidative Damage in Neurological Disorders, P113