Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106530
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dc.contributor.authorMonteiro-Alfredo, Tamaeh-
dc.contributor.authorMatafome, Paulo N.-
dc.contributor.authorIacia, Bianca Pancoti-
dc.contributor.authorAntunes, Kátia Ávila-
dc.contributor.authorDos Santos, Jéssica Maurino-
dc.contributor.authorda Silva Melo da Cunha, Janielle-
dc.contributor.authorOliveira, Sara-
dc.contributor.authorOliveira, Alex Santos-
dc.contributor.authorCampos, Jaqueline Ferreira-
dc.contributor.authorMagalhães, Mariana-
dc.contributor.authorCabral, Célia-
dc.contributor.authorSeiça, Raquel-
dc.contributor.authorCardoso, Cláudia Andrea Lima-
dc.contributor.authorde Oliveira, Caio Fernando Ramalho-
dc.contributor.authorDos Santos, Edson Lucas-
dc.contributor.authorde Picoli Souza, Kely-
dc.date.accessioned2023-04-06T10:43:25Z-
dc.date.available2023-04-06T10:43:25Z-
dc.date.issued2020-
dc.identifier.issn1942-0900pt
dc.identifier.issn1942-0994pt
dc.identifier.urihttps://hdl.handle.net/10316/106530-
dc.description.abstractOxidative stress is a metabolic disorder linked with several chronic diseases, and this condition can be improved by natural antioxidants. The fruit pulp of the palm Acrocomia aculeata (Jacq.) Lodd. ex Mart. is widely used in the treatment of various illnesses, but as far as we know, there are no reports regarding the properties of its leaves. Thus, we aimed to evaluate the antioxidant activity of A. aculeata leaf extracts obtained with water (EA-Aa), ethanol (EE-Aa), and methanol (EM-Aa) solvents. The extracts were chemically characterized, and their antioxidant activity was assessed through the scavenging of the free radicals DPPH and ABTS. EE-Aa and EM-Aa showed the highest amounts of phenolic compounds and free radical scavenging activity. However, EA-Aa was more efficient to protect human erythrocytes against AAPH-induced hemolysis and lipid peroxidation. Thus, we further show the antioxidant effect of EA-Aa in preventing AAPH-induced protein oxidation, H2O2-induced DNA fragmentation, and ROS generation in Cos-7 cells. Increased levels of Sirt1, catalase, and activation of ERK and Nrf2 were observed in Cos-7 treated with EA-Aa. We also verify increased survival in nematodes C. elegans, when induced to the oxidative condition by Juglone. Therefore, our results showed a typical chemical composition of plants for all extracts, but the diversity of compounds presented in EA-Aa is involved in the lower toxicity and antioxidant properties provided to the macromolecules tested, proteins, DNA, and lipids. This protective effect also proven in Cos-7 and in C. elegans was probably due to the activation of the Sirt1/Nrf2 pathway. Altogether, the low toxicity and the antioxidant properties of EA-Aa showed in all the experimental models support its further use in the treatment of oxidative stress-related diseases.pt
dc.language.isoengpt
dc.publisherHindawipt
dc.relationFundação de Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT)pt
dc.relationCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt
dc.relationUID/NEU/04539/2013pt
dc.relationUID/NEU/04539/2019pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshFruitpt
dc.subject.meshHumanspt
dc.subject.meshOxidative Stresspt
dc.subject.meshPlant Leavespt
dc.subject.meshSirtuin 1pt
dc.titleAcrocomia aculeata (Jacq.) Lodd. ex Mart. Leaves Increase SIRT1 Levels and Improve Stress Resistancept
dc.typearticle-
degois.publication.firstPage5238650pt
degois.publication.lastPage16pt
degois.publication.titleOxidative Medicine and Cellular Longevitypt
dc.peerreviewedyespt
dc.identifier.doi10.1155/2020/5238650pt
degois.publication.volume2020pt
dc.date.embargo2020-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitICBR Coimbra Institute for Clinical and Biomedical Research-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitICBR Coimbra Institute for Clinical and Biomedical Research-
crisitem.author.parentresearchunitFaculty of Medicine-
crisitem.author.parentresearchunitFaculty of Medicine-
crisitem.author.orcid0000-0001-5514-0797-
crisitem.author.orcid0000-0002-3422-290X-
crisitem.author.orcid0000-0003-4562-6683-
crisitem.author.orcid0000-0002-8378-0895-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D CFE - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
I&D CIBIT - Artigos em Revistas Internacionais
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