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

被引:177
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
相关论文
共 67 条
[61]   Chronic nicotine treatment enhances focal ischemic brain injury and depletes free pool of brain microvascular tissue plasminogen activator in rats [J].
Wang, L ;
Kittaka, M ;
Sun, N ;
Schreiber, SS ;
Zlokovic, BV .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (02) :136-146
[62]   VEGF increases BMEC monolayer permeability by affecting occludin expression and tight junction assembly [J].
Wang, W ;
Dentler, WL ;
Borchardt, RT .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2001, 280 (01) :H434-H440
[63]   Effects of hypoxia-reoxygenation on rat blood-brain barrier permeability and tight junctional protein expression [J].
Witt, KA ;
Mark, KS ;
Hom, S ;
Davis, TP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (06) :H2820-H2831
[64]   Localization of claudin-3 in tight junctions of the blood-brain barrier is selectively lost during experimental autoimmune encephalomyelitis and human glioblastoma multiforme [J].
Wolburg, H ;
Wolburg-Buchholz, K ;
Kraus, J ;
Rascher-Eggstein, G ;
Liebner, S ;
Hamm, S ;
Duffner, F ;
Grote, EH ;
Risau, W ;
Engelhardt, B .
ACTA NEUROPATHOLOGICA, 2003, 105 (06) :586-592
[65]   Microarray analysis of nicotine-induced changes in gene expression in endothelial cells [J].
Zhang, SL ;
Day, INM ;
Ye, S .
PHYSIOLOGICAL GENOMICS, 2001, 5 (04) :187-192
[66]   Nicotine induced changes in gene expression by human coronary artery endothelial cells [J].
Zhang, SL ;
Day, I ;
Ye, S .
ATHEROSCLEROSIS, 2001, 154 (02) :277-283
[67]   Nicotine increases plasminogen activator inhibitor-1 production by human brain endothelial cells via protein kinase C-associated pathway [J].
Zidovetzki, R ;
Chen, PJ ;
Fisher, M ;
Hofman, FM .
STROKE, 1999, 30 (03) :651-655