Vitamin A exhibits potent antiamyloidogenic and fibril-destabilizing effects in vitro

被引:115
作者
Ono, K
Yoshiike, Y
Takashima, A
Hasegawa, K
Naiki, H
Yamada, M
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Neurol & Neurobiol Aging, Kanazawa, Ishikawa 9208640, Japan
[2] RIKEN, Brain Sci Inst, Lab Alzheimers Dis, Wako, Saitama 3510198, Japan
[3] Fukui Med Univ, Dept Pathol, Fukui 9101193, Japan
[4] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama 3320012, Japan
关键词
Alzheimer's disease; vitamin A; beta-amyloid fibrils; thioflavin T; electron microscopy; cytotoxicity;
D O I
10.1016/j.expneurol.2004.05.035
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cerebral deposition of amyloid-peptide (Abeta) in the brain is an invariant feature of Alzheimer disease (AD). Plasma or cerebrospinal fluid concentrations of antioxidant vitamins and carotenoids, such as vitamins A, C, E, and beta-carotene, have been reported to be lower in AD patients, and these vitamins clinically have been demonstrated to slow the progression of dementia. In this study, we used fluorescence spectroscopy with thioflavin T (ThT) and electron microscopy to examine the effects of vitamin A (retinol, retinal, and retinoic acid), beta-carotene, and vitamins B2, B6, C, and E on the formation, extension, and destabilization of beta-amyloid fibrils (fAbeta) in vitro. Among them, vitamin A and beta-carotene dose-dependently inhibited formation of fAbeta from fresh Abeta, as well as their extension. Moreover, they dose-dependently destabilized preformed fAbetas. The overall activity of the molecules examined was in the order of retinol = retinal > beta-carotene > retinoic acid. Although the exact mechanisms are still unclear, vitamins A and beta-carotene could be key molecules for the prevention and therapy of AD. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:380 / 392
页数:13
相关论文
共 81 条
[1]   Amyloid β protein inhibits cellular MTT reduction not by suppression of mitochondrial succinate dehydrogenase but by acceleration of MTT formazan exocytosis in cultured rat cortical astrocytes [J].
Abe, K ;
Saito, H .
NEUROSCIENCE RESEARCH, 1998, 31 (04) :295-305
[2]   Inhibition of glutathione depletion by retinoic acid and tocopherol protects cultured neurons from staurosporine-induced oxidative stress and apoptosis [J].
Ahlemeyer, B ;
Krieglstein, J .
NEUROCHEMISTRY INTERNATIONAL, 2000, 36 (01) :1-5
[3]   Neuroprotective abilities of resveratrol and other red wine constituents against nitric oxide-related toxicity in cultured hippocampal neurons [J].
Bastianetto, S ;
Zheng, WH ;
Quirion, R .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (04) :711-720
[4]   VITAMIN-E PROTECTS NERVE-CELLS FROM AMYLOID BETA-PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, J ;
COLE, GM ;
SCHUBERT, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) :944-950
[5]   HYDROGEN-PEROXIDE MEDIATES AMYLOID-BETA PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, JB ;
LESLEY, R ;
SCHUBERT, D .
CELL, 1994, 77 (06) :817-827
[6]  
Bilski P, 2000, PHOTOCHEM PHOTOBIOL, V71, P129, DOI 10.1562/0031-8655(2000)071&lt
[7]  
0129:SIPVBP&gt
[8]  
2.0.CO
[9]  
2
[10]  
Bohles H, 1997, INT J VITAM NUTR RES, V67, P321