Inhibition of the Self-Assembly of Aβ and of Tau by Polyphenols: Mechanistic Studies

被引:55
|
作者
Zheng, Qiuchen [1 ]
Kebede, Micheal T. [1 ]
Kemeh, Merc M. [1 ]
Islam, Saadman [1 ]
Lee, Bethany [1 ]
Bleck, Stuart D. [1 ]
Wurfl, Liliana A. [1 ]
Lazo, Noel D. [1 ]
机构
[1] Clark Univ, Carlson Sch Chem & Biochem, 950 Main St, Worcester, MA 01610 USA
来源
MOLECULES | 2019年 / 24卷 / 12期
基金
美国国家卫生研究院;
关键词
Alzheimer ' s disease; amyloid-beta self-assembly; tau self-assembly; tau hyperphosphorylation; amyloid assemblies; neurofibrillary tangles; polyphenols; PAIRED HELICAL FILAMENTS; AMYLOID PRECURSOR PROTEIN; IN-VITRO; GALLIC ACID; HYPERPHOSPHORYLATED TAU; CEREBRAL AMYLOIDOSIS; SYNAPTIC DYSFUNCTION; MOLECULAR-MECHANISM; ALPHA-SECRETASE; MOUSE MODEL;
D O I
10.3390/molecules24122316
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
The amyloid-beta (A beta) peptide and tau protein are thought to play key neuropathogenic roles in Alzheimer's disease (AD). Both A beta and tau self-assemble to form the two major pathological hallmarks of AD: amyloid plaques and neurofibrillary tangles, respectively. In this review, we show that naturally occurring polyphenols abundant in fruits, vegetables, red wine, and tea possess the ability to target pathways associated with the formation of assemblies of A beta and tau. Polyphenols modulate the enzymatic processing of the amyloid-beta precursor protein and inhibit toxic A beta oligomerization by enhancing the clearance of A beta 42 monomer, modulating monomer-monomer interactions and remodeling oligomers to non-toxic forms. Additionally, polyphenols modulate tau hyperphosphorylation and inhibit tau beta-sheet formation. The anti-A beta-self-assembly and anti-tau-self-assembly effects of polyphenols increase their potential as preventive or therapeutic agents against AD, a complex disease that involves many pathological mechanisms.
引用
收藏
页数:20
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