Impaired metabotropic glutamate receptor phospholipase C signaling pathway in the cerebral cortex in Alzheimer's disease and dementia with Lewy bodies correlates with stage of Alzheimer's-disease-related changes

被引:97
作者
Albasanz, JL
Dalfó, E
Ferrer, I
Martín, M
机构
[1] Univ Castilla La Mancha, Ctr Reg Invest Biomed, Area Bioquim, Fac Ciencias Quim,Dept Quim Inorgan Organ & Bioqu, E-13071 Ciudad Real, Spain
[2] Univ Bellvitge, Inst Neuropatol, Serv Anat Patol, IDIBELL, Lhospitalet De Llobregat, Spain
[3] Univ Barcelona, Hosp Llobregat, Fac Med, Dept Biol Celular & Anat Patol, Barcelona, Spain
关键词
dementia with Lewy bodies; Alzheimer's disease; metabotropic glutamate receptor; phospholipase C;
D O I
10.1016/j.nbd.2005.05.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The aim of the present work was to analyze the status of metabotropic glutamate receptors (mGluRs) in the frontal cortex (area 8) from ten cases with common form DLB (eDLB) and eleven cases with pure AD in comparison with five age-matched controls. mGluRs, determined by radioligand binding assays, were significantly decreased in cerebral cortex in eDLB. This decrease was already present in cases with early AD changes not involving the frontal cortex, but dramatically correlated with AD neuropathological changes, at its greatest in isocortical stages, which was associated with a decrease in the expression levels of mGluR(I) detected by Western blotting. Moreover, mGluRs analyzed in pure AD were lower than those obtained in cDLB and also correlated with progression of illness. On the other hand, the expression levels of phospholipase C beta(1) (PLC beta(1)) isoform, which is the effector of group I mGluRs, was decreased in parallel in cDLB cases. Finally, the PLC beta(1) decrease was associated with reduced GTP- and L-glutamate-stimulated PLC activity in both cDLB and AD cases. These results show that group I mGluRs/PLC signaling are down-regulated and desensitized in the frontal cortex in cDLB and AD cases and that these modifications worsen with progression of AD changes in the cerebral neocortex. Therefore, group I mGluR dysfunction may be implicated in the pathogenesis of cognitive impairment and dementia in common form of DLB and pure AD. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:685 / 693
页数:9
相关论文
共 62 条
  • [11] Pharmacology and functions of metabotropic glutamate receptors
    Conn, PJ
    Pin, JP
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1997, 37 : 205 - 237
  • [12] Nicotinic receptor abnormalities in Alzheimer's disease
    Court, J
    Martin-Ruiz, C
    Piggott, M
    Spurden, D
    Griffiths, M
    Perry, E
    [J]. BIOLOGICAL PSYCHIATRY, 2001, 49 (03) : 175 - 184
  • [13] Cowburn RF, 2001, BIOCHEM SOC SYMP, V67, P163
  • [14] Dalfó E, 2004, BRAIN PATHOL, V14, P388
  • [15] Glutamate uptake
    Danbolt, NC
    [J]. PROGRESS IN NEUROBIOLOGY, 2001, 65 (01) : 1 - 105
  • [16] FERRER I, 2002, NEURODEGENER DIS, P83
  • [17] CORTICAL PYRAMIDAL NEURON LOSS MAY CAUSE GLUTAMATERGIC HYPOACTIVITY AND COGNITIVE IMPAIRMENT IN ALZHEIMERS-DISEASE - INVESTIGATIVE AND THERAPEUTIC PERSPECTIVES
    FRANCIS, PT
    SIMS, NR
    PROCTER, AW
    BOWEN, DM
    [J]. JOURNAL OF NEUROCHEMISTRY, 1993, 60 (05) : 1589 - 1604
  • [18] Glutamatergic systems in Alzheimer's disease
    Francis, PT
    [J]. INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 2003, 18 : S15 - S21
  • [19] The cholinergic hypothesis of Alzheimer's disease: a review of progress
    Francis, PT
    Palmer, AM
    Snape, M
    Wilcock, GK
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 66 (02) : 137 - 147
  • [20] EXCITATORY AMINO-ACIDS AND ALZHEIMERS-DISEASE
    GREENAMYRE, JT
    YOUNG, AB
    [J]. NEUROBIOLOGY OF AGING, 1989, 10 (05) : 593 - 602