Chronic psychotropic drug treatment causes differential expression of connexin 43 and GFAP in frontal cortex of rats

被引:56
作者
Fatemi, S. Hossein [1 ,2 ,3 ]
Folsom, Timothy D. [1 ]
Reutiman, Teri J. [1 ]
Pandian, Twinkle [1 ,4 ]
Braun, Natalie N. [1 ]
Haug, Kari [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Psychiat, Div Neurosci Res, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Pharmacol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Neurosci, Minneapolis, MN 55455 USA
[4] Mayo Clin & Mayo Fdn, Mayo Med Sch, Rochester, MN 55905 USA
关键词
connexin; 43; GFAP; rat; prefrontal cortex; schizophrenia; autism;
D O I
10.1016/j.schres.2008.05.016
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Astrocytic markers glial fibrillary acidic protein (GFAP) and connexin 43 (CX43) are known to have altered expression ill brains of subjects with psychiatric disorders including autism and major depression. The current study investigated whether GFAP and CX43 expressions are affected by several commonly used psychotropic medications (clozapine, fluoxetine, haloperidol, lithium, olanzapine, and valproic acid). Using SDS-PAGE and western blotting technique, we observed that CX43 protein expression in prefrontal cortex was significantly increased following chronic treatment with fluoxetine and clozapine, while it was significantly decreased by haloperidol and lithium. GFAP protein expression was significantly decreased following chronic treatment with clozapine and valproic acid. These results suggest that astroglial markers GFAP and CX43 could be potential targets for therapeutic intervention. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 134
页数:8
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