2011
DOI: 10.1016/j.neuint.2011.02.010
|View full text |Cite
|
Sign up to set email alerts
|

Oleuropein and derivatives from olives as Tau aggregation inhibitors

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

4
94
0

Year Published

2012
2012
2024
2024

Publication Types

Select...
7
2
1

Relationship

1
9

Authors

Journals

citations
Cited by 147 publications
(98 citation statements)
references
References 45 publications
4
94
0
Order By: Relevance
“…We found that the presence of OleA during wt-TTR and L55P-TTR aggregation pathway induced an increase of Trp quenching, suggesting that the effect of OleA in stabilizing meta-stable intermediate states relies on the reduction of the overall surface hydrophobicity of the aggregates ( Figure 2). OleA does not prevent TTR aggregation by itself but, rather, it is effective in counteracting mature fibrils growth, a behaviour comparable with previously data shown with tau [27], amylin [9] and Abeta peptides [10]. The reported data suggest that OleA induces some remodelling of the supramolecular structure of the growing aggregates.…”
Section: Oleuropein Aglycone Reduces Transthyretin Fibrils Formationsupporting
confidence: 85%
“…We found that the presence of OleA during wt-TTR and L55P-TTR aggregation pathway induced an increase of Trp quenching, suggesting that the effect of OleA in stabilizing meta-stable intermediate states relies on the reduction of the overall surface hydrophobicity of the aggregates ( Figure 2). OleA does not prevent TTR aggregation by itself but, rather, it is effective in counteracting mature fibrils growth, a behaviour comparable with previously data shown with tau [27], amylin [9] and Abeta peptides [10]. The reported data suggest that OleA induces some remodelling of the supramolecular structure of the growing aggregates.…”
Section: Oleuropein Aglycone Reduces Transthyretin Fibrils Formationsupporting
confidence: 85%
“…The former three sites correspond to the AT8 epitope, as recently redefined on the basis of the AT8 Fab crystal structure in complex with the triply phosphorylated peptide (15), and hence suggest the antibody, clinically used to stage the disease progression (10), indeed immunostains a Tau species that can aggregate without any other factors. Whereas the quest for aggregation inhibitors has been mainly performed with heparin as an external aggregation inducer (46)(47)(48)(49), our present description of a phosphorylation-driven Tau aggregation assay opens up new avenues and should allow retesting of the previously defined classes of molecules or the discovery of potentially more specific molecules that counteract the aggregation of phosphorylated Tau.…”
Section: Discussionmentioning
confidence: 99%
“…The potential of OLE in the context of AD is corroborated also by its ability to inhibit the fibrillization of tau (both wild-type and carrying the P301L mutation, a mutation that increases its aggregation propensity and leads to frontotemporal dementia and parkinsonism in carriers) leading to reduced deposition of fibrillar material in the form of short rods (TEM analysis) (Daccache et al 2011). The IC50 of OLE for the inhibition of P301L tau aggregation was 1.3 M, as determined by the Thioflavin-S (ThS) fluorescence assay; in contrast, HT was poorly effective, inducing the growth of fibrils that were less dense but structurally similar to those originated in the absence of any inhibitor, thus confirming the superiority of the secoiridoid as an anti-amyloid agent.…”
Section: 3mentioning
confidence: 99%