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Molecules ; 24(12)2019 Jun 22.
Article in English | MEDLINE | ID: mdl-31234523

ABSTRACT

The amyloid-ß (Aß) peptide and tau protein are thought to play key neuropathogenic roles in Alzheimer's disease (AD). Both Aß 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 Aß and tau. Polyphenols modulate the enzymatic processing of the amyloid-ß precursor protein and inhibit toxic Aß oligomerization by enhancing the clearance of Aß42 monomer, modulating monomer-monomer interactions and remodeling oligomers to non-toxic forms. Additionally, polyphenols modulate tau hyperphosphorylation and inhibit tau ß-sheet formation. The anti-Aß-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.


Subject(s)
Amyloid beta-Peptides/metabolism , Polyphenols/pharmacology , Protein Aggregates/drug effects , Protein Multimerization/drug effects , tau Proteins/metabolism , Amyloid beta-Peptides/chemistry , Animals , Humans , Models, Molecular , Molecular Structure , Phosphorylation , Polyphenols/chemistry , Protein Aggregation, Pathological/drug therapy , Protein Binding , Structure-Activity Relationship , tau Proteins/chemistry
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