Differential modulation of gene expression in the NMDA postsynaptic density of schizophrenic and control smokers

S. Mexal , M. Frank , R. Berger , C.E. Adams , R.G. Ross , R. Freedman , S. Leonard
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引用次数: 95

Abstract

Nicotine is known to induce the release of multiple neurotransmitters, including glutamate and dopamine, through activation of nicotinic receptors. Gene expression in the N-methyl-d-aspartate postsynaptic density (NMDA-PSD), as well as other functional groups, was compared in postmortem hippocampus of schizophrenic and nonmentally ill smokers and nonsmokers utilizing a microarray and quantitative RT-PCR approach. The expression of 277 genes was significantly changed between all smokers and nonsmokers. Specific gene groups, most notably genes expressed in the NMDA-PSD, were prevalent among these transcripts. Analysis of the interaction between smoking and schizophrenia identified several genes in the NMDA-PSD that were differentially affected by smoking in patients. The present findings suggest that smoking may differentially modulate glutamatergic function in schizophrenic patients and control subjects. The biological mechanisms underlying chronic tobacco use are likely to differ substantially between these two groups.

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精神分裂症和对照组吸烟者突触后密度NMDA基因表达的差异调节
众所周知,尼古丁通过激活尼古丁受体,诱导多种神经递质的释放,包括谷氨酸和多巴胺。利用微阵列和定量RT-PCR方法比较了精神分裂症和非精神疾病吸烟者和非吸烟者死后海马中n -甲基-d-天冬氨酸突触后密度(NMDA-PSD)以及其他功能群的基因表达。277个基因的表达在所有吸烟者和非吸烟者之间都发生了显著变化。在这些转录本中普遍存在特定的基因群,尤其是在NMDA-PSD中表达的基因。对吸烟和精神分裂症之间相互作用的分析发现,NMDA-PSD中的几个基因在患者中受到吸烟的不同影响。目前的研究结果表明,吸烟可能对精神分裂症患者和对照组的谷氨酸能功能有不同的调节作用。慢性烟草使用的生物学机制可能在这两组之间存在很大差异。
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