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Volume 21, Issue 8, Pages 726-735 (August 2010)


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Oleuropein aglycon prevents cytotoxic amyloid aggregation of human amylin

Stefania RigacciaCorresponding Author Informationemail address, Valentina Guidottia, Monica Bucciantiniac, Matteo Parria, Chiara Nediania, Elisabetta Cerbaib, Massimo Stefaniac, Andrea Bertiac

Received 3 December 2008; received in revised form 6 April 2009; accepted 22 April 2009. published online 21 July 2009.

Abstract 

Pancreatic amyloid deposits of amylin are a hallmark of Type II diabetes and considerable evidence indicates that amylin oligomers are cytotoxic to β-cells. Many efforts are presently spent to find out naturally occurring molecules, or to design synthetic ones, able to hinder amylin aggregation or to protect cells against aggregate cytotoxicity. In this context, a protective effect of some polyphenols against amyloid cytotoxicity was reported. Actually dietary polyphenols are endowed with multiple health benefits, and extra virgin olive oil is attracting increasing interest as a source of these substances. Here, we investigated the effects on amylin aggregation and cytotoxicity of the secoiridoid oleuropein aglycon, the main phenolic component of extra virgin olive oil. We found that oleuropein, when present during the aggregation of amylin, consistently prevented its cytotoxicity to RIN-5F pancreatic β-cells, as determined by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide test and caspase-3 activity assay. A lack of interaction with the cell membrane of amylin aggregates grown in the presence of oleuropein was shown by fluorescence microscopy and synthetic lipid vesicle permeabilization. Moreover, our ThT assay, circular dichroism analysis and electron microscopy images suggested that oleuropein interferes with amylin aggregation, resulting in a different path skipping the formation of toxic pre-fibrillar aggregates. These results provide a molecular basis for some of the benefits potentially coming from extra virgin olive oil consumption and pave the way to further studies on the possible pharmacological use of oleuropein to prevent or to slow down the progression of type II diabetes.

a Department of Biochemical Sciences, University of Florence, Viale Morgagni 50, 50134 Florence, Italy

b Department of Preclinical and Clinical Pharmacology, University of Florence, Viale Pieraccini 6, 50139 Florence, Italy

c Research Center on the Molecular Basis of Neurodegeneration, Viale Morgagni, 50, 50134 Florence, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 055 4598346; fax: +39 055 4598905.

 This work was supported by a grant from the Ente Cassa di Risparmio di Firenze and from the Italian MIUR (grant n. 2007XY59ZJ_001).

PII: S0955-2863(09)00100-4

doi:10.1016/j.jnutbio.2009.04.010


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