Evidence for physiological down-regulation of brain oxidative phosphorylation in Alzheimer's disease

被引:96
作者
Chandrasekaran, K [1 ]
Hatanpaa, K [1 ]
Brady, DR [1 ]
Rapoport, SI [1 ]
机构
[1] NCI,NIH,NEUROSCI LAB,BETHESDA,MD 20892
关键词
D O I
10.1006/exnr.1996.0180
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In vivo imaging of patients with Alzheimer's disease using positron emission tomography (PET) demonstrates progressive reductions in brain glucose metabolism and blood flow in relation to dementia severity, more so in association than primary cortical regions, These reductions likely follow regional synaptic loss or dysfunction and reflect physiological down-regulation of gene expression for glucose delivery, oxidative phosphorylation (OXPHOS), and energy consumption in brain, Indeed, the pattern of down-regulation of expression for both mitochondrial and nuclear genes coding for subunits of OXPHOS enzymes in the Alzheimer brain resembles the pattern of down-regulation in normal brain caused by chronic sensory deprivation. In both cases, do cvn-regulation likely is mediated by changes in transcriptional and posttranscriptional regulatory factors, Physiological down-regulation of OXPHOS gene expression in Alzheimer's is consistent with PET evidence that cognitive or psychophysical activation of mildly to moderately demented Alzheimer's patients can augment brain-blood flow and glucose metabolism to the same extent as in control subjects, If the primary neuronal defect that leads to reduced brain energy demand in Alzheimer's disease could be prevented or treated, brain glucose transport and OXPHOS enzyme activities might recover to normal levels. (C) 1996 Academic Press, Inc.
引用
收藏
页码:80 / 88
页数:9
相关论文
共 103 条
  • [1] ROLE OF ABNORMALLY PHOSPHORYLATED TAN IN THE BREAKDOWN OF MICROTUBULES IN ALZHEIMER-DISEASE
    ALONSO, AD
    ZAIDI, T
    GRUNDKEIQBAL, I
    IQBAL, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) : 5562 - 5566
  • [2] MITOCHONDRIAL DECAY IN AGING
    AMES, BN
    SHIGENAGA, MK
    HAGEN, TM
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1995, 1271 (01): : 165 - 170
  • [3] BIOGENESIS OF MITOCHONDRIA
    ATTARDI, G
    SCHATZ, G
    [J]. ANNUAL REVIEW OF CELL BIOLOGY, 1988, 4 : 289 - 333
  • [4] REGULATION OF MITOCHONDRIAL GENE-EXPRESSION IN MAMMALIAN-CELLS
    ATTARDI, G
    CHOMYN, A
    KING, MP
    KRUSE, B
    POLOSA, PL
    MURDTER, NN
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (04) : 509 - 513
  • [5] BLASS JP, 1991, REV NEUROL, V147, P513
  • [6] ENHANCED EXPRESSION OF THE BLOOD-BRAIN-BARRIER GLUT1 GLUCOSE-TRANSPORTER GENE BY BRAIN-DERIVED FACTORS
    BOADO, RJ
    WANG, L
    PARDRIDGE, WM
    [J]. MOLECULAR BRAIN RESEARCH, 1994, 22 (1-4): : 259 - 267
  • [7] GLUCOSE DEPRIVATION CAUSES POSTTRANSCRIPTIONAL ENHANCEMENT OF BRAIN CAPILLARY ENDOTHELIAL GLUCOSE TRANSPORTER GENE-EXPRESSION VIA GLUT1 MESSENGER-RNA STABILIZATION
    BOADO, RJ
    PARDRIDGE, WM
    [J]. JOURNAL OF NEUROCHEMISTRY, 1993, 60 (06) : 2290 - 2296
  • [8] A LIFETIME OF RETINAL LIGHT EXPOSURE DOES NOT APPEAR TO INCREASE MITOCHONDRIAL MUTATIONS
    BODENTEICH, A
    MITCHELL, LG
    MERRILL, CR
    [J]. GENE, 1991, 108 (02) : 305 - 309
  • [9] FINE-STRUCTURAL LOCALIZATION OF POTASSIUM-STIMULATED PARA-NITROPHENYLPHOSPHATASE ACTIVITY IN DENDRITES OF CEREBRAL-CORTEX
    BRODERSON, SH
    PATTON, DL
    STAHL, WL
    [J]. JOURNAL OF CELL BIOLOGY, 1978, 77 (02) : R13 - R17
  • [10] ORGANIZATION OF MITOCHONDRIA IN OLFACTORY-BULB GRANULE CELL DENDRITIC SPINES
    CAMERON, HA
    KALISZEWSKI, CK
    GREER, CA
    [J]. SYNAPSE, 1991, 8 (02) : 107 - 118