Levels of mRNAs encoding synaptic vesicle and synaptic plasma membrane proteins in the temporal cortex of elderly schizophrenic patients

被引:65
作者
Sokolov, BP
Tcherepanov, AA
Haroutunian, V
Davis, KL
机构
[1] NIDA, Mol Neurobiol Branch, NIH, Baltimore, MD 21224 USA
[2] Mt Sinai Sch Med, Dept Psychiat, New York, NY USA
关键词
Schizophrenia; temporal cortex; synaptic proteins; gene expression; synaptic organization; mRNA;
D O I
10.1016/S0006-3223(00)00875-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Electron microscopy and biochemical studies indicate that developmental abnormalities in synaptic organization may be present in brains of schizophrenic patients. This study determined whether these synaptic abnormalities are reflected in differential or uniform alterations in the expression of various synaptic protein genes in the left superior temporal gyrus of schizophrenic patients. Methods: Levels of nRNAs encoding four synaptic vesicle proteins (synaptotagmin 1 [p65], rab3a, synaptobrevin 1, and synaptobrevin 2) and two synaptic plasma membrane proteins (syntaxin 1A and SNAP-25) were measured post-mortem in the left superior temporal gyrus from elderly (58-95 years) schizophrenic patients (n = 14) and age-matched control subjects (n = 9). Results: There were significant negative correlations between age and levels of synaptotagmin 1 (p65), rab3a, synaptobrevin 1, SNAP-25 and syntaxin 1A mRNAs in schizophrenic patients (-.692 < r < -.517, .003 < p < .030) but not in control subjects. Levels of all six synaptic mRNAs studied were increased in the younger (58-79 years) subgroup of schizophrenic patients compared to control subjects and older (80-95 years) subgroup of schizophrenic patients. Conclusions: That similar abnormalities were found for mRNAs encoding different synaptic vesicle and synaptic plasma membrane proteins suggests that they reflect overall neurodevelopmental abnormalities in synaptic connectivity in the temporal cortex of schizophrenic patients rather than changes in the number of synaptic vesicles per synapse or abnormalities in a specific synaptic function. Biol Psychiatry 2000;48:184-196 (C) 2000 Society of Biological Psychiatry.
引用
收藏
页码:184 / 196
页数:13
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