Immunohistochemical analysis of human brain suggests pathological synergism of Alzheimer's disease and diabetes mellitus

被引:190
作者
Valente, Tony [2 ]
Gella, Alejandro [1 ]
Fernandez-Busquets, Xavier [3 ,4 ]
Unzeta, Mercedes [2 ]
Durany, Nuria [1 ]
机构
[1] Univ Int Catalunya, Fac Med & Hlth Sci, Sant Cugat Del Valles 08195, Spain
[2] Autonomous Univ Barcelona, Sch Med, Dept Biochem & Mol Biol, Inst Neurosci, E-08193 Barcelona, Spain
[3] Univ Barcelona, Nanobioengn Grp, Inst Bioengn Catalonia, E-08028 Barcelona, Spain
[4] Univ Barcelona, Biomol Interact Team, Nanosci & Nanotechnol Inst, E-08028 Barcelona, Spain
关键词
Abeta; Alzheimer's disease; RAGE; AGEs; Diabetes; Immunohistochemistry; GLYCATION END-PRODUCTS; OXIDATIVE STRESS; NONENZYMATIC GLYCOSYLATION; AMYLOID FIBRILS; AGE-INHIBITORS; CROSS-LINKING; A-BETA; RECEPTOR; ENDPRODUCTS; PEPTIDE;
D O I
10.1016/j.nbd.2009.09.008
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
It has been extensively reported that diabetes mellitus (DM) patients have a higher risk of developing Alzheimer's disease (AD). but a mechanistic connection between both pathologies has not been provided so far Carbohydrate-derived advanced glycation endproducts (AGEs) have been implicated in the chronic complications of DM and have been reported to play an important role in the pathogenesis of AD. The earliest histopathological manifestation of AD is the apparition of extracellular aggregates of the amyloid beta peptide (A beta). To investigate possible correlations between AGEs and A beta aggregates with both pathologies. we have performed an immuhistochemical study in human post-mortem samples of AD, AD with diabetes (ADD). diabetic and nondemented controls ADD brains showed increased number of A beta dense plaques and receptor for AGEs (RACE)-positive and Tau-positive cells, higher AGEs levels and major microglial activation, compared to AD brain. Our results indicate that ADD patients present a significant increase of cell damage through a RAGE-dependent mechanism, suggesting that AGEs may promote the generation of an oxidative stress vicious cycle, which can explain the severe progression of patients with both pathologies (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:67 / 76
页数:10
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