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Oleuropein aglycone: A polyphenol with different targets against amyloid toxicity
Authors:Manuela Leri  Reiner Oropesa-Nuñez  Claudio Canale  Sara Raimondi  Sofia Giorgetti  Elena Bruzzone  Vittorio Bellotti  Massimo Stefani  Monica Bucciantini
Affiliation:1. Department of Biomedical, Experimental and Clinical Sciences ''Mario Serio'', University of Florence, Viale Morgagni, 50 50134 Florence, Italy;2. Department of Neuroscience, Psychology, Area of Medicine and Health of the Child of the University of Florence, Viale Pieraccini, 6, 50139 Florence, Italy;3. Department of Physics, University of Genova, via Dodecaneso 33, 16146, Genova, Italy;4. Department of Molecular Medicine, Institute of Biochemistry, University of Pavia, Viale Taramelli 3/B, 27100 Pavia, Italy;5. Wolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, Division of Medicine Royal Free Campus, University College London, NW3 2PF London, UK;6. Interuniversity Center for the Study of Neurodegenerative Diseases (CIMN), Florence, Italy
Abstract:

Background

Many data highlight the benefits of the Mediterranean diet and its main lipid component, extra-virgin olive oil (EVOO). EVOO contains many phenolic compounds that have been found effective against several aging- and lifestyle-related diseases, including neurodegeneration. Oleuropein, a phenolic secoiroid glycoside, is the main polyphenol in the olive oil. It has been reported that the aglycone form of Oleuropein (OleA) interferes in vitro and in vivo with amyloid aggregation of a number of proteins/peptides involved in amyloid, particularly neurodegenerative, diseases avoiding the growth of toxic oligomers and displaying protection against cognitive deterioration.

Methods

In this study, we carried out a cellular and biophysical study on the relationships between the effects of OleA on the aggregation and cell interactions of the D76N β2-microglobulin (D76N b2m) variant associated with a familial form of systemic amyloidosis with progressive bowel dysfunction and extensive visceral amyloid deposits.

Results

Our results indicate that OleA protection against D76N b2m cytotoxicity results from i) a modification of the conformational and biophysical properties of its amyloid fibrils; ii) a modification of the cell bilayer surface properties of exposed cells.

Conclusions

This study reveals that OleA remodels not only D76N b2m aggregates but also the cell membrane interfering with the misfolded proteins-cell membrane association, in most cases an early event triggering amyloid–mediated cytotoxicity.

General significance

The data provided in the present article focus on OleA protection, featuring this polyphenol as a promising plant molecule useful against amyloid diseases.
Keywords:ANS  8-anilinonaphthalene-1-sulfonic acid  EVOO  extra-virgin olive oil  OleA  Oleuropein aglycone  MD  Mediterranean diet  DMSO  dimethyl sulfoxide  Oleuropein aglycone  Amyloid  β2-microglobulin  D76N variant
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