Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/27747
Title: Identification of polyphenolic compounds and black tea extract as potent inhibitors of lipid membrane destabilization by AB42 aggregates
Authors: Gauci, Alison J.
Caruana, Mario
Giese, Armin
Scerri, Charles
Vassallo, Neville
Keywords: Alzheimer's disease
Amyloid beta-protein
Liposomes
Oligomers
Polyphenols
Issue Date: 2011
Publisher: IOS Press
Citation: Gauci, A. J., Caruana, M., Giese, A., Scerri, C., & Vassallo, N. (2011). Identification of polyphenolic compounds and black tea extract as potent inhibitors of lipid membrane destabilization by AB42 aggregates. Journal of Alzheimer’s Disease, 27, 767–779.
Abstract: Amyloid-β (Aβ) aggregation is a recognized key process in the pathogenesis of Alzheimer's disease (AD). Misfolded Aβ peptides self-assemble into higher-order oligomers that compromise membrane integrity, leading to synaptic degeneration and neuronal cell death. The main aim of this study was to explore whether small-molecule compounds and black tea extract can protect phospholipid membranes from disruption by Aβ aggregates. We first established a robust protocol for aggregating Aβ₄₂ peptides into a range of oligomers that efficiently permeabilized small unilamellar liposomes. Next, 15 natural plant polyphenolic compounds, 8 N'-benzylidene-benzohydrazide (NBB) compounds and black tea extract were assessed for their ability to antagonize liposome permeabilization by the Aβ₄₂ oligomers. Our data indicates that black tea extract, the flavones apigenin and baicalein, and the stilbene nordihydroguaiaretic acid (NDGA) are indeed potent inhibitors. Taking into consideration the results of all the small-molecule polyphenols and NBB compounds, it can be proposed that a dihydroxyphenyl ring structure, alone or as part of a flavone scaffold, is particularly effective for protection against membrane damage by the Aβ₄₂ oligomers. Given the critical role of membrane perforation in the neurodegenerative cascade, these conclusions may guide the design and development of novel therapeutic drugs in AD.
URI: https://www.um.edu.mt/library/oar//handle/123456789/27747
Appears in Collections:Scholarly Works - FacM&SPat
Scholarly Works - FacM&SPB

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