mRNAs for clozapine-sensitive receptors co-localize in rat prefrontal cortex neurons

被引:46
|
作者
Vysokanov, A
Flores-Hernandez, J
Surmeier, DJ
机构
[1] Northwestern Univ, Sch Med, Dept Physiol, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Inst Neurosci, Chicago, IL 60611 USA
关键词
prefrontal cortex; single cell RT-PCR; interneurons; GABA; pyramidal neurons; dopamine; acetylcholine; serotonin; schizophrenia;
D O I
10.1016/S0304-3940(98)00882-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The clinical efficacy of clozapine in treating schizophrenia may stem from its lack of receptor selectivity. If true, several clozapine-sensitive receptors may be co-expressed by neurons dysfunctional in schizophrenia. To test this hypothesis, neurons from the rat medial prefrontal cortex were acutely isolated and subjected to single cell RT-PCR analysis. The cc-ordinated expression of five clozapine-sensitive receptors (D-4, m1, 5-HT2a, 5-HT2c, 5-HT7) was examined in interneurons and pyramidal neurons. Profiling of GABAergic interneurons commonly revealed the co-expression of two or more clozapine-sensitive receptor mRNAs. Although co-expression of these receptors was less extensive in pyramidal neurons, it was also commonly found. These results suggest that clozapine's therapeutic effects may be mediated by antagonism of dopaminergic, cholinergic and serotoninergic signaling pathways at the single cell level. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:179 / 182
页数:4
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