Decreased numerical density of kainate receptor-positive neurons in the orbitofrontal cortex of chronic schizophrenics

被引:19
作者
Garey, L. J. [1 ]
Von Bussmann, K. A.
Hirsch, S. R.
机构
[1] Univ Lausanne, Ctr Psychiat Neurosci, CH-1008 Lausanne, Switzerland
[2] Marshall House Surg, Hitchin SG5 1LH, England
[3] Univ London Imperial Coll Sci & Technol, Fac Med, Div Neurosci & Psychol Med, London W6 8RF, England
关键词
postmortem; cerebral cortex; glutamate receptors; kainate; schizophrenia;
D O I
10.1007/s00221-006-0396-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We utilised postmortem brain tissue to quantify sections of left and right orbitofrontal cortex (area 11) from nine schizophrenic and eight control patients from the Charing Cross Prospective Schizophrenia Study immunostained for the presence of the kainate receptor (GluR5/6/7). The numerical density of neurons immunopositive for kainate receptor was measured. Other sections from the same blocks were stained with cresyl violet to determine the total neuronal numerical density. All measurements were made blind: diagnoses were only revealed by a third party after measurements were completed. There was a significant reduction (21%) in numerical density of kainate receptor-positive neurons in both cortices in the schizophrenic group (488 cells/mm(2)) compared to that in the control group (618 cells/mm(2)) (P=0.033). Nissl-stained tissue showed no significant difference in total neuronal numerical density between control and schizophrenic groups. These observations suggest that there are actually fewer kainate receptor-positive neurons in schizophrenic orbitofrontal cortex. There was no correlation of reduced kainate receptor-positive cell number with age at death, postmortem interval, or other possibly confounding neuropathology. Our results support the concept of there being reduced glutamatergic activity in frontal cortex in schizophrenia.
引用
收藏
页码:234 / 242
页数:9
相关论文
共 64 条
[1]   GENE-EXPRESSION FOR GLUTAMIC-ACID DECARBOXYLASE IS REDUCED WITHOUT LOSS OF NEURONS IN PREFRONTAL CORTEX OF SCHIZOPHRENICS [J].
AKBARIAN, S ;
KIM, JJ ;
POTKIN, SG ;
HAGMAN, JO ;
TAFAZZOLI, A ;
BUNNEY, WE ;
JONES, EG .
ARCHIVES OF GENERAL PSYCHIATRY, 1995, 52 (04) :258-266
[2]   SYNAPTIC REARRANGEMENTS IN MEDIAL PREFRONTAL CORTEX OF HALOPERIDOL-TREATED RATS [J].
BENES, FM ;
PASKEVICH, PA ;
DAVIDSON, J ;
DOMESICK, VB .
BRAIN RESEARCH, 1985, 348 (01) :15-20
[3]   GluR5,6,7 subunit immunoreactivity on apical pyramidal cell dendrites in hippocampus of schizophrenics and manic depressives [J].
Benes, FM ;
Todtenkopf, MS ;
Kostoulakos, P .
HIPPOCAMPUS, 2001, 11 (05) :482-491
[4]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[5]  
BRODMANN K, 2005, VERGLEICHENDE LOKALI
[6]  
CROW TJ, 1989, ARCH GEN PSYCHIAT, V46, P1145
[7]   FRONTAL CORTICAL AND LEFT TEMPORAL GLUTAMATERGIC DYSFUNCTION IN SCHIZOPHRENIA [J].
DEAKIN, JFW ;
SLATER, P ;
SIMPSON, MDC ;
GILCHRIST, AC ;
SKAN, WJ ;
ROYSTON, MC ;
REYNOLDS, GP ;
CROSS, AJ .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (06) :1781-1786
[8]   MICROZONAL DECREASES IN THE IMMUNOSTAINING FOR NON-NMDA IONOTROPIC EXCITATORY AMINO-ACID RECEPTOR SUBUNITS GLUR-2/3 AND GLUR-5/6/7 IN THE HUMAN EPILEPTOGENIC NEOCORTEX [J].
DEFELIPE, J ;
HUNTLEY, GW ;
DELRIO, MR ;
SOLA, RG ;
MORRISON, JH .
BRAIN RESEARCH, 1994, 657 (1-2) :150-158
[9]  
DEUTSCH SI, 1988, CLIN NEUROPHARMACOL, V12, P1
[10]   The effect of chronic haloperidol treatment on glutamate receptor subunit (GluR1, GluR2, KA1, KA2, NR1) mRNAs and glutamate binding protein mRNA in rat forebrain [J].
Eastwood, SL ;
Porter, RHP ;
Harrison, PJ .
NEUROSCIENCE LETTERS, 1996, 212 (03) :163-166