Proteomic identification of less oxidized brain proteins in aged senescence-accelerated mice following administration of antisense oligonucleotide directed at the Aβ region of amyloid precursor protein

被引:67
作者
Poon, HF
Farr, SA
Banks, WA
Pierce, WM
Klein, JB
Morley, JE
Butterfield, DA [1 ]
机构
[1] Univ Kentucky, Ctr Membrane Sci, Dept Chem, Lexington, KY 40506 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40506 USA
[3] GRECC, VA Med Ctr, St Louis, MO 63106 USA
[4] St Louis Univ, Sch Med, Div Geriatr Med, Dept Internal Med, St Louis, MO 63110 USA
[5] Univ Louisville, Sch Med, Dept Pharmacol, Louisville, KY 40292 USA
[6] VAMC, Louisville, KY 40292 USA
[7] Univ Louisville, Sch Med, Kidney Dis Program, Louisville, KY 40292 USA
[8] Univ Louisville, Sch Med, Proteom Core Lab, Louisville, KY 40292 USA
来源
MOLECULAR BRAIN RESEARCH | 2005年 / 138卷 / 01期
关键词
proteomic identification; SAMP8; amyloid precursor protein; antisense oligonucleotide; amyloid beta-peptide; Alzheimer's disease; oxidative stress;
D O I
10.1016/j.molbrainres.2005.02.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Amyloid beta-peptide (A beta) is the major constituent of senile plaques, a pathological hallmark of Alzheimer ' s disease (AD) brain. It is generally accepted that A beta plays a central role in the pathophysiology of AD. A beta is released from cells under entirely normal cellular conditions during the internalization and endosornal processing of amyloid precursor protein (APP), However. accumulation of A beta can induce neurotoxicity, Our previous reports showed that decreasing the production of A beta by giving an intracerebroventricular injection of a 4.2-mer phosphorothiolated antisense oligonucleotide (AO) directed at the A beta region of the APP gene reduces lipid peroxidation and protein oxidation and improves cognitive deficits in aged senescence-accelerated mice prone X (SAMP8) mice, In order to investigate how A beta level reduction improves learning and memory performance of SAMP8 mice through reduction of oxidative stress in brains, we used proteomics to identify the proteins that are less oxidized in 12-month-old SAMP8 mice brains treated with AO against the All, region of APP (12 mA) compared to that of the age-control SAMP8 mice. We found that the specific protein carbonyl levels of aldoase 3 (Aldo3), coronin I a (Corola) and peroxiredoxin 2 (Prdx2) are significantly decreased in the brains or 12 mA SAMP8 mice compared to the age-controlled SAMP8 treated with random AO (12 mR). We also found that the expression level of alpha-ATP synthase (Atp5a1) was significantly decreased, whereas the expression of profilin 2 (Pro-2) was significantly increased in brains from 12 mA SAMP8 mice, Our results suggest that decreasing A beta levels in aged brain in aged accelerated mice may contribute to the mechanism of restoring the learning and memory improvement in aged SAMP8 mice and may provide insight into the role of A beta in the memory and cognitive deficits in AD. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 16
页数:9
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