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

Brain Res Mol Brain Res. 2005 Oct 3;139(2):317-32. doi: 10.1016/j.molbrainres.2005.06.006.

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.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Analysis of Variance
  • Blotting, Northern / methods
  • Blotting, Western / methods
  • Female
  • Gene Expression / physiology*
  • Humans
  • Male
  • Microarray Analysis / methods
  • Middle Aged
  • Models, Biological
  • Postmortem Changes
  • RNA, Messenger / biosynthesis
  • Receptors, N-Methyl-D-Aspartate / genetics
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Schizophrenia / metabolism
  • Schizophrenia / physiopathology*
  • Smoking / metabolism
  • Smoking / physiopathology*
  • alpha Catenin / metabolism

Substances

  • CTNNA2 protein, human
  • RNA, Messenger
  • Receptors, N-Methyl-D-Aspartate
  • alpha Catenin