Nicotine increases in vivo blood-brain barrier permeability and alters cerebral microvascular tight junction protein distribution

被引:169
|
作者
Hawkins, BT
Abbruscato, TJ
Egleton, RD
Brown, RC
Huber, JD
Campos, CR
Davis, TP
机构
[1] Univ Arizona, Coll Med, Program Neurosci, Tucson, AZ 85724 USA
[2] Texas Tech Univ, Ctr Hlth Sci, Sch Pharm, Dept Pharmaceut Sci, Amarillo, TX 79106 USA
[3] Univ Arizona, Coll Med, Dept Pharmacol, Tucson, AZ 85724 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol, Houston, TX 77030 USA
[5] W Virginia Univ, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
关键词
blood brain barrier; nicotine; tight junction; ZO-1; ZO-2; claudin;
D O I
10.1016/j.brainres.2004.08.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The blood-brain barrier (BBB) is critical to the health of the central nervous system. The BBB is formed primarily by the presence of tight junctions (TJ) between cerebral microvessel endothelial cells. In light of the known effects of nicotine on endothelial cell biology, the specific effects of nicotine on the in vivo BBB were examined. Using in situ brain perfusion, it was found that continuous administration of nicotine (4.5 mg free base (.) kg(-1) (.) day(-1)) for 1 and 7 days led to increased permeability of the BBB to [C-14]-sucrose without significant changes in its initial volume of distribution. The expression and distribution of the TJ-associated proteins actin, occludin, claudin-1, -3, and -5, and ZO-1 and -2 were analyzed by Western blot and immunofluorescence microscopy. Though no changes in total protein expression were observed, nicotine treatment was associated with altered cellular distribution of ZO-1 and diminished junctional immunoreactivity of claudin-3. It is proposed that nicotine leads to changes in BBB permeability via the modulation of TJ proteins. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:48 / 58
页数:11
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