Gene expression profiles of metabolic enzyme transcripts in Alzheimer's disease

被引:127
作者
Brooks, Wendy M.
Lynch, Patrick J.
Ingle, Catherine C.
Hatton, Alexander
Emson, Piers C.
Faull, Richard L. M.
Starkey, Mike P.
机构
[1] MRC, Rosalind Franklin Ctr Genom Res, Hinxton CB10 1SB, Cambs, England
[2] Babraham Inst, Lab Mol Neurosci, Cambridge CB2 4AT, England
[3] Univ Auckland, Dept Anat Radiol, Fac Med & Hlth Sci, Auckland 1, New Zealand
关键词
Alzheimer's disease; gene expression; glycolysis; TCA cycle; oxidative phosphorylation; energy metabolism;
D O I
10.1016/j.brainres.2006.09.106
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The successfully functioning brain is a heavy user of metabolic energy. Alzheimer's disease, in which cognitive faculties decline, may be due, at least in part, to metabolic insufficiency. Using microarray analysis and quantitative RT-PCR, the expression of mRNA transcripts involved in glucose metabolism was investigated in Alzheimer's diseased post-mortem human hippocampal samples. of the 51 members of the glycolytic, tricarboxylic acid cycle, oxidative phosphorylation, and associated pathways investigated by qPCR, 15 were confirmed to be statistically significantly (p < 0.05) down-regulated in Alzheimer's disease. This finding suggests that reductions in the levels of transcripts encoded by genes that participate in energy metabolism may be involved in Alzheimer's disease. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
相关论文
共 52 条
[1]
Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease [J].
Anchisi, D ;
Borroni, B ;
Franceschi, M ;
Kerrouche, N ;
Kalbe, E ;
Beuthien-Beumann, B ;
Cappa, S ;
Lenz, O ;
Ludecke, S ;
Marcone, A ;
Mielke, R ;
Ortelli, P ;
Padovani, A ;
Pelati, O ;
Pupi, A ;
Scarpini, E ;
Weisenbach, S ;
Herholz, K ;
Salmon, E ;
Holthoff, V ;
Sorbi, S ;
Fazio, F ;
Perani, D .
ARCHIVES OF NEUROLOGY, 2005, 62 (11) :1728-1733
[2]
CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]
Further evidence for LBP-1c/CP2/LSF association in Alzheimer's disease families [J].
Bertram, L ;
Parkinson, M ;
McQueen, MB ;
Mullin, K ;
Hsiao, M ;
Menon, R ;
Moscarillo, TJ ;
Blacker, D ;
Tanzi, RE .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (11) :857-862
[4]
Evidence for genetic linkage of Alzheimer's disease to chromosome 10q [J].
Bertram, L ;
Blacker, D ;
Mullin, K ;
Keeney, D ;
Jones, J ;
Basu, S ;
Yhu, S ;
McInnis, MG ;
Go, RCP ;
Vekrellis, K ;
Selkoe, DJ ;
Saunders, AJ ;
Tanzi, RE .
SCIENCE, 2000, 290 (5500) :2302-+
[5]
Incipient Alzheimer's disease: Microarray correlation analyses reveal major transcriptional and tumor suppressor responses [J].
Blalock, EM ;
Geddes, JW ;
Chen, KC ;
Porter, NM ;
Markesbery, WR ;
Landfield, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) :2173-2178
[6]
The role of the metabolic lesion in Alzheimer's disease [J].
Blass, John P. ;
Gibson, Gary E. ;
Hoyer, Siegfried .
JOURNAL OF ALZHEIMERS DISEASE, 2002, 4 (03) :225-232
[7]
Blass JP, 2000, ANN NY ACAD SCI, V924, P170
[8]
Mitochondrial abnormalities in Alzheimer brain: Mechanistic implications [J].
Bubber, P ;
Haroutunian, V ;
Fisch, G ;
Blass, JP ;
Gibson, GE .
ANNALS OF NEUROLOGY, 2005, 57 (05) :695-703
[9]
Huntington and DRPLA proteins selectively interact with the enzyme GAPDH [J].
Burke, JR ;
Enghild, JJ ;
Martin, ME ;
Jou, YS ;
Myers, RM ;
Roses, AD ;
Vance, JM ;
Strittmatter, WJ .
NATURE MEDICINE, 1996, 2 (03) :347-350
[10]
Amyloid-β induces disulfide bonding and aggregation of GAPDH in Alzheimer's disease [J].
Cumming, RC ;
Schubert, D .
FASEB JOURNAL, 2005, 19 (11) :2060-+