Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/106520
Título: An Anthocyanin-Rich Extract Obtained from Portuguese Blueberries Maintains Its Efficacy in Reducing Microglia-Driven Neuroinflammation after Simulated Digestion
Autor: Serra, Diana 
Henriques, Joana F. 
Serra, Teresa
Silva, Andreia Bento
Bronze, Maria Rosário
Dinis, Teresa C. P. 
Almeida, Leonor M. 
Palavras-chave: neuroinflammation; anthocyanins; phenolic acids; in vitro digestion; microglia; NF-kB; STAT1; ROS
Data: 28-Nov-2020
Editora: MDPI
Projeto: POCI-01-0145-FEDER-029089 (Anthocyanins4ASD) 
PTDC/SAU-NUT/29089/2017 
UIDB/04539/2020 
LISBOA-01-0145-FEDER-402-022125 
Título da revista, periódico, livro ou evento: Nutrients
Volume: 12
Número: 12
Resumo: Dietary polyphenols are multi-target compounds that have been considered promising candidates in strategies for the mitigation of neurological diseases, acting particularly through reduction of microglia-driven neuroinflammation. In this study, an anthocyanin-rich extract obtained from Portuguese blueberries was subjected to a simulated gastrointestinal digestion; after chemical characterisation, the potential of both non-digested and digested extracts to combat neuroinflammation was evaluated using a microglia N9 cell line. Although the extracts have markedly different chemical composition, both were efficient in reducing the production of either key inflammatory markers or reactive oxygen species and in enhancing reduced glutathione levels in activated cells. Furthermore, this protection was shown to be related to the suppression of nuclear factor kappa B (NF-kB) activation, and to a signal transducer and activator of transcription 1 (STAT1)-independent mechanism. These results demonstrate that the anthocyanin extract, after simulated digestion, maintains its efficacy against neuroinflammation, and can, therefore, assume a relevant role in prevention of neuroinflammation-related neurological disorders.
URI: https://hdl.handle.net/10316/106520
ISSN: 2072-6643
DOI: 10.3390/nu12123670
Direitos: openAccess
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