Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/103080
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dc.creatorStephanie Andrade
dc.creatorJoana A. Loureiro
dc.creatorManuel A. N. Coelho
dc.creatorMaria do Carmo Pereira
dc.date.accessioned2022-09-08T20:43:22Z-
dc.date.available2022-09-08T20:43:22Z-
dc.date.issued2015
dc.identifier.othersigarra:145125
dc.identifier.urihttps://hdl.handle.net/10216/103080-
dc.description.abstractThe amyloid cascade hypothesis suggests that dysfunction and neuronal death in the brain is caused by the deposition of amyloid beta-peptide (A beta) in the Alzheimer's disease (AD). The peptide is aggregated as amyloid fibrils within the neuritic plaques and vascular deposits that characterize the disease. Thus, it is essential to find molecules that prevent or interrupt this aggregation process. Various natural compounds have been suggested as therapeutics for AD. Among these compounds, resveratrol (RES) arouses great interest in the therapy of AD. In this study the structure and fibril assembly of the A beta((1-42)) were analyzed in the presence of different sources of RES. The results demonstrated that A beta((1-42)) forms fibrils with different morphologies depending on the RES provenience. Moreover, TEM analysis and Thioflavin T fluorescence assay suggest that the presence of the resveratrol present in the grape skin retards or even inhibits the aggregation of the peptide.
dc.language.isoeng
dc.relation.ispartofProceedings - 2015 IEEE 4th Portuguese Meeting on Bioengineering, ENBENG 2015
dc.rightsrestrictedAccess
dc.titleInteraction studies of amyloid beta-peptide with the natural compound resveratrol
dc.typeArtigo em Livro de Atas de Conferência Internacional
dc.contributor.uportoFaculdade de Engenharia
dc.identifier.doi10.1109/enbeng.2015.7088833
dc.identifier.authenticusP-00G-4SN
Appears in Collections:FEUP - Artigo em Livro de Atas de Conferência Internacional

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