THE HUMAN ENTORHINAL CORTEX - NORMAL MORPHOLOGY AND LAMINA-SPECIFIC PATHOLOGY IN VARIOUS DISEASES

被引:265
作者
BRAAK, H
BRAAK, E
机构
[1] Department of Anatomy, J.W. Goethe University, Frankfurt
关键词
ALLOCORTEX; ENTORHINAL REGION; DEMENTIA; ALZHEIMERS DISEASE; PARKINSONS DISEASE; PROGRESSIVE SUPRANUCLEAR PALSY; DEMENTIA WITH ARGYROPHILIC GRAINS; HUNTINGTONS DISEASE;
D O I
10.1016/0168-0102(92)90014-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The entorhinal territory consists of the entorhinal and transentorhinal regions spreading over the ambient gyrus and anterior portions of the parahippocampal gyrus. The transentorhinal region mediates between the adjoining temporal isocortex laterally and the entorhinal region medially. The entorhinal cortex consists of a molecular layer, followed by an external principal stratum, a cell-sparse lamina dissecans, an internal principal stratum and - within he underlying white matter - a profound cellular layer. The principal strata can each be divided into three layers Pre alpha, beta, gamma, and Pri alpha, beta, gamma. Data obtained from experimental investigations in monkeys reveal that the entorhinal territory serves as a relay station for information from both isocortical association areas and centers of the limbic system. After processing within the entorhinal cortex, this information is transferred to the hippocampal formation via the perforant path. Pathological changes within the entorhinal territory impair this continuous data transfer and contribute to a decline of cognitive functions. Entorhinal involvement associated with impaired cognitive functions is described in cases of Alzheimer's disease, Parkinson's disease, progressive supranuclear palsy, dementia with argyrophilic grains and Huntington's disease.
引用
收藏
页码:6 / 31
页数:26
相关论文
共 124 条
  • [51] Presbyophrenic dementia, its anatomical basis and clinical demarcation
    Fischer, O
    [J]. ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1910, 3 : 371 - 471
  • [52] FORNO LS, 1982, MOVEMENT DISORD, P25
  • [53] FREEDMAN M, 1985, HDB CLIN NEUROLOGY, V2, P311
  • [54] FRIEDERICHECSY B, 1988, CELL TISSUE RES, V254, P361
  • [55] GALLYAS F, 1971, ACTA MORPHOL HUNG, V19, P1
  • [56] GAMBETTI P, 1990, INT CONGR SER, V884, P57
  • [57] TAU-PROTEINS OF ALZHEIMER PAIRED HELICAL FILAMENTS - ABNORMAL PHOSPHORYLATION OF ALL 6 BRAIN ISOFORMS
    GOEDERT, M
    SPILLANTINI, MG
    CAIRNS, NJ
    CROWTHER, RA
    [J]. NEURON, 1992, 8 (01) : 159 - 168
  • [58] Grunthal E, 1930, HDB GEISTESKRANKHEIT, V11, P638
  • [59] Hayden MR., 1981, HUNTINGTONS CHOREA, P45
  • [60] ALZHEIMERS-DISEASE - CELL-SPECIFIC PATHOLOGY ISOLATES THE HIPPOCAMPAL-FORMATION
    HYMAN, BT
    VANHOESEN, GW
    DAMASIO, AR
    BARNES, CL
    [J]. SCIENCE, 1984, 225 (4667) : 1168 - 1170