DIFFERENTIAL SYNAPTIC LOSS IN THE CORTEX IN ALZHEIMERS-DISEASE - A STUDY USING ARCHIVAL MATERIAL

被引:36
作者
CLINTON, J
BLACKMAN, SEA
ROYSTON, MC
ROBERTS, GW
机构
[1] SMITHKLINE BEECHAM,DEPT MOLEC NEUROPATHOL,HARLOW CM19 5AD,ESSEX,ENGLAND
[2] ST MARYS HOSP,IMPERIAL COLL,SCH MED,DEPT ANAT,SERIOUS MENTAL AFFLICT RES TEAM,LONDON W2 1PG,ENGLAND
[3] CHARING CROSS & WESTMINSTER MED SCH,DEPT PSYCHIAT & ANAT,LONDON W6 8RP,ENGLAND
关键词
ALZHEIMERS DISEASE; SYNAPTIC LOSS; SNAP-25; ARCHIVAL MATERIAL; IMMUNOCYTOCHEMISTRY; IMAGE ANALYSIS;
D O I
10.1097/00001756-199401120-00032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
WE have developed techniques to utilize immunocytochemical localization of synaptic protein (SNAP-25) in conjunction with image analysis to investigate synaptic loss in readily available archival material. Sections from 5 cortical regions were examined in cases of Alzheimer's disease (n = 7) and controls (n = 5). Image analysis was used to determine a relative synaptic index (RSI) and probe for changes in synaptic integrity. RSI value for cortical regions did not differ in controls. RSIs from sulci and gyri were significantly correlated in Brodmann areas 6, 9 and 18 (40 and 52 approached significance). Cases with Alzheimer's disease showed decreases in sulcal and gyral RSI values of between 60% (Brodmann area 6 < 0.01) and 10% (Brodmann area 18 > 0.4) and a lack of correlation in sulco-gyral values except in Brodmann area 18. We have demonstrated that synaptic pathology is heterogeneous with frontal cortex most and occipital cortex least affected. Sulci and gyri are affected to different degrees. The underlying cytoarchitecture of the cortex and its pattern of connectivity appears to have a considerable influence on the degree and extent of synaptic pathology.
引用
收藏
页码:497 / 500
页数:4
相关论文
共 25 条
[1]  
BARBOSAPAULA MM, 1986, ACTA NEUROL SCAND, V74, P404
[2]   MORPHOLOGICAL ADAPTIVE RESPONSE OF THE SYNAPTIC JUNCTIONAL ZONES IN THE HUMAN DENTATE GYRUS DURING AGING AND ALZHEIMERS-DISEASE [J].
BERTONIFREDDARI, C ;
FATTORETTI, P ;
CASOLI, T ;
MEIERRUGE, W ;
ULRICH, J .
BRAIN RESEARCH, 1990, 517 (1-2) :69-75
[3]   SYNAPTIC DEGENERATION IS THE PRIMARY NEUROPATHOLOGICAL FEATURE IN PRION DISEASE - A PRELIMINARY-STUDY [J].
CLINTON, J ;
FORSYTH, C ;
ROYSTON, MC ;
ROBERTS, GW .
NEUROREPORT, 1993, 4 (01) :65-68
[4]   A QUANTITATIVE MORPHOMETRIC ANALYSIS OF THE NEURONAL AND SYNAPTIC CONTENT OF THE FRONTAL AND TEMPORAL CORTEX IN PATIENTS WITH ALZHEIMERS-DISEASE [J].
DAVIES, CA ;
MANN, DMA ;
SUMPTER, PQ ;
YATES, PO .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1987, 78 (02) :151-164
[5]  
EASTWOOD SL, 1993, IN PRESS NEUROSCIENC
[6]   SOLUBLE BETA-AMYLOID PRECURSOR PROTEIN AND PYRAMIDAL NEURON LOSS [J].
FRANCIS, PT ;
WEBSTER, MT ;
PROCTER, AW ;
CLARKE, NA ;
BOWEN, DM ;
DOSHI, R ;
MANN, DMA ;
NEARY, D .
LANCET, 1993, 341 (8842) :431-431
[7]   QUANTITATIVE DIFFERENCES IN THE DEPOSITION OF BETA A4 PROTEIN IN THE SULCI AND GYRI OF FRONTAL AND TEMPORAL ISOCORTEX IN ALZHEIMERS-DISEASE [J].
GENTLEMAN, SM ;
ALLSOP, D ;
BRUTON, CJ ;
JAGOE, R ;
POLAK, JM ;
ROBERTS, GW .
NEUROSCIENCE LETTERS, 1992, 136 (01) :27-30
[8]   EM STUDY OF THE NUMBERS OF CORTICAL SYNAPSES IN THE BRAINS OF AGING PEOPLE AND PEOPLE WITH ALZHEIMER-TYPE DEMENTIA [J].
GIBSON, PH .
ACTA NEUROPATHOLOGICA, 1983, 62 (1-2) :127-133
[9]   SYNAPTIC LOSS IN ALZHEIMERS-DISEASE AND OTHER DEMENTIAS [J].
HAMOS, JE ;
DEGENNARO, LJ ;
DRACHMAN, DA .
NEUROLOGY, 1989, 39 (03) :355-361
[10]   TISSUE FIXATION METHODS ALTER THE IMMUNOHISTOCHEMICAL DEMONSTRABILITY OF SYNAPTOPHYSIN [J].
HOOG, A ;
GOULD, VE ;
GRIMELIUS, L ;
FRANKE, WW ;
FALKMER, S ;
CHEJFEC, G .
ULTRASTRUCTURAL PATHOLOGY, 1988, 12 (06) :673-678