Phencyclidine-induced changes in rat cortical gene expression identified by microarray analysis: implications for schizophrenia

被引:23
作者
Kaiser, S
Foltz, LA
George, CA
Kirkwood, SC
Bemis, KG
Lin, X
Gelbert, LM
Nisenbaum, LK [1 ]
机构
[1] Eli Lilly & Co, Lilly Res Lab, Neurosci Discovery Res, Indianapolis, IN 46285 USA
[2] Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
[3] Lilly Corp Ctr, Lilly Res Labs, Global Statist Sci, Indianapolis, IN 46285 USA
[4] Eli Lilly & Co, Lilly Res Lab, Indianapolis, IN 46285 USA
关键词
psychotomimetic; brain cortex; animal model; false discovery rate; GeneChip;
D O I
10.1016/j.nbd.2004.01.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acute phencyclidine induces schizophrenia-like symptoms in healthy humans and psychotic episodes in schizophrenics. Although phencyclidine is known as a N-methyl D-aspartate receptor antagonist (NMDA-R), the molecular events underlying the behavioral symptoms remain largely unknown. Statistical analysis of oligonucleotide microarray data was used to identify phencyclidine-induced alterations in rat cortical gene expression. Acute phencyclidine produced a statistically significant change in 477 genes in rat prefrontal cortex (PFC), a brain area associated with cognitive dysfunction in schizophrenics. Real-time quantitative PCR (RTQ-PCR) confirmed a subset of these changes ranging from -59% to 255% (smallest confirmation: -19%). Subsequent time-course and dose-response studies using RTQ-PCR confirmed and extended the original microarray results. At the molecular level, genes altered by phencyclidine are related to diverse biological processes including stress, inflammatory response, growth and development, neural plasticity and signal transduction. Further analysis, aimed at assessing the relevance of our results to schizophrenia, revealed dysregulation of genes related to: (i) thalamocortical projections, (ii) neurotransmission and neuromodulation, (iii) thyroid hormone activity, (iv) oligodendrocyte linage, (v) brain lipid metabolism, (vi) sleep architecture and (viii) the velocardiofacial syndrome. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:220 / 235
页数:16
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