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Anti-Amyloidogenic Properties of Some Phenolic Compounds
A family of 21 polyphenolic compounds consisting of those found naturally in danshen and their analogues were synthesized and subsequently screened for their anti-amyloidogenic activity against the amyloid beta peptide (Aβ(42)) of Alzheimer’s disease. After 24 h incubation with Aβ(42), five compound...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496683/ https://www.ncbi.nlm.nih.gov/pubmed/25898401 http://dx.doi.org/10.3390/biom5020505 |
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author | Porzoor, Afsaneh Alford, Benjamin Hügel, Helmut M. Grando, Danilla Caine, Joanne Macreadie, Ian |
author_facet | Porzoor, Afsaneh Alford, Benjamin Hügel, Helmut M. Grando, Danilla Caine, Joanne Macreadie, Ian |
author_sort | Porzoor, Afsaneh |
collection | PubMed |
description | A family of 21 polyphenolic compounds consisting of those found naturally in danshen and their analogues were synthesized and subsequently screened for their anti-amyloidogenic activity against the amyloid beta peptide (Aβ(42)) of Alzheimer’s disease. After 24 h incubation with Aβ(42), five compounds reduced thioflavin T (ThT) fluorescence, indicative of their anti-amyloidogenic propensity (p < 0.001). TEM and immunoblotting analysis also showed that selected compounds were capable of hindering fibril formation even after prolonged incubations. These compounds were also capable of rescuing the yeast cells from toxic changes induced by the chemically synthesized Aβ(42). In a second assay, a Saccharomyces cerevisiae AHP1 deletant strain transformed with GFP fused to Aβ(42) was treated with these compounds and analyzed by flow cytometry. There was a significant reduction in the green fluorescence intensity associated with 14 compounds. We interpret this result to mean that the compounds had an anti-amyloid-aggregation propensity in the yeast and GFP-Aβ(42) was removed by proteolysis. The position and not the number of hydroxyl groups on the aromatic ring was found to be the most important determinant for the anti-amyloidogenic properties. |
format | Online Article Text |
id | pubmed-4496683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44966832015-07-10 Anti-Amyloidogenic Properties of Some Phenolic Compounds Porzoor, Afsaneh Alford, Benjamin Hügel, Helmut M. Grando, Danilla Caine, Joanne Macreadie, Ian Biomolecules Article A family of 21 polyphenolic compounds consisting of those found naturally in danshen and their analogues were synthesized and subsequently screened for their anti-amyloidogenic activity against the amyloid beta peptide (Aβ(42)) of Alzheimer’s disease. After 24 h incubation with Aβ(42), five compounds reduced thioflavin T (ThT) fluorescence, indicative of their anti-amyloidogenic propensity (p < 0.001). TEM and immunoblotting analysis also showed that selected compounds were capable of hindering fibril formation even after prolonged incubations. These compounds were also capable of rescuing the yeast cells from toxic changes induced by the chemically synthesized Aβ(42). In a second assay, a Saccharomyces cerevisiae AHP1 deletant strain transformed with GFP fused to Aβ(42) was treated with these compounds and analyzed by flow cytometry. There was a significant reduction in the green fluorescence intensity associated with 14 compounds. We interpret this result to mean that the compounds had an anti-amyloid-aggregation propensity in the yeast and GFP-Aβ(42) was removed by proteolysis. The position and not the number of hydroxyl groups on the aromatic ring was found to be the most important determinant for the anti-amyloidogenic properties. MDPI 2015-04-17 /pmc/articles/PMC4496683/ /pubmed/25898401 http://dx.doi.org/10.3390/biom5020505 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Porzoor, Afsaneh Alford, Benjamin Hügel, Helmut M. Grando, Danilla Caine, Joanne Macreadie, Ian Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title | Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title_full | Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title_fullStr | Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title_full_unstemmed | Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title_short | Anti-Amyloidogenic Properties of Some Phenolic Compounds |
title_sort | anti-amyloidogenic properties of some phenolic compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496683/ https://www.ncbi.nlm.nih.gov/pubmed/25898401 http://dx.doi.org/10.3390/biom5020505 |
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