Resveratrol promotes clearance of Alzheimer's disease amyloid-β peptides

被引:572
作者
Marambaud, P [1 ]
Zhao, HT [1 ]
Davies, P [1 ]
机构
[1] N Shore Long Isl Jewish Inst Med Res, Litwin Zucker Res Ctr Study Alzheimers Dis & Memo, Manhasset, NY 11030 USA
关键词
D O I
10.1074/jbc.M508246200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several epidemiological studies indicate that moderate consumption of wine is associated with a lower incidence of Alzheimer's disease. Wine is enriched in antioxidant compounds with potential neuroprotective activities. However, the exact molecular mechanisms involved in the beneficial effects of wine intake on the neurodegenerative process in Alzheimer's disease brain remain to be clearly defined. Here we show that resveratrol ( trans-3,4',5-trihydroxystilbene), a naturally occurring polyphenol mainly found in grapes and red wine, markedly lowers the levels of secreted and intracellular amyloid-beta(A beta) peptides produced from different cell lines. Resveratrol does not inhibit A beta production, because it has no effect on the A beta-producing enzymes beta- and gamma-secretases, but promotes instead intracellular degradation of A beta via amechanism that involves the proteasome. Indeed, the resveratrol-induced decrease of A beta could be prevented by several selective proteasome inhibitors and by siRNA-directed silencing of the proteasome subunit beta 5. These findings demonstrate a proteasome-dependent anti-amyloidogenic activity of resveratrol and suggest that this natural compound has a therapeutic potential in Alzheimer's disease.
引用
收藏
页码:37377 / 37382
页数:6
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共 34 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   A cell biological perspective on Alzheimer's disease [J].
Annaert, W ;
De Strooper, B .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2002, 18 :25-51
[3]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[4]   Characterization of new polyclonal antibodies specific for 40 and 42 amino acid long amyloid beta peptides: Their use to examine the cell biology of presenilins and the immunohistochemistry of sporadic Alzheimer's disease and cerebral amyloid angiopathy cases [J].
Barelli, HL ;
Lebeau, A ;
Vizzavona, J ;
Delaere, P ;
Chevallier, N ;
Drouot, C ;
Marambaud, P ;
Ancolio, K ;
Buxbaum, JD ;
Khorkova, O ;
Heroux, J ;
Sahasrabudhe, S ;
Martinez, J ;
Warter, JM ;
Mohr, M ;
Checler, F .
MOLECULAR MEDICINE, 1997, 3 (10) :695-707
[5]   trans-3,4,5′-trihydroxystibene inhibits hypoxia-inducible factor 1α and vascular endothelial growth factor expression in human ovarian cancer cells [J].
Cao, ZX ;
Fang, J ;
Xia, C ;
Shi, XL ;
Jiang, BH .
CLINICAL CANCER RESEARCH, 2004, 10 (15) :5253-5263
[6]  
CHECLER F, 1995, J NEUROCHEM, V65, P1431
[7]   Protein quality control in Alzheimer's disease by the ubiquitin proteasome system [J].
de Vrij, FMS ;
Fischer, DF ;
van Leeuwen, FW ;
Hol, EM .
PROGRESS IN NEUROBIOLOGY, 2004, 74 (05) :249-270
[8]   Towards subunit-specific proteasome inhibitors:: synthesis and evaluation of peptide α′,β′-epoxyketones [J].
Elofsson, M ;
Splittgerber, U ;
Myung, J ;
Mohan, R ;
Crews, CM .
CHEMISTRY & BIOLOGY, 1999, 6 (11) :811-822
[9]   AMYLOID BETA-PROTEIN INHIBITS UBIQUITIN-DEPENDENT PROTEIN-DEGRADATION IN-VITRO [J].
GREGORI, L ;
FUCHS, C ;
FIGUEIREDOPEREIRA, ME ;
VANNOSTRAND, WE ;
GOLDGABER, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (34) :19702-19708
[10]   SIR2 and aging - the exception that proves the rule [J].
Guarente, L .
TRENDS IN GENETICS, 2001, 17 (07) :391-392