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Digested galactoglucomannan mitigates oxidative stress in human cells, restores gut bacterial diversity, and provides chemopreventive protection against colon cancer in rats

dc.contributor.authordos Santos Lima, Amanda
dc.contributor.authorde Oliveira Pedreira, Fernanda Rafaelly
dc.contributor.authorBento, Nathália Alves
dc.contributor.authorNovaes, Rômulo Dias
dc.contributor.authordos Santos, Elda Gonçalves
dc.contributor.authorde Almeida Lima, Graziela Domingues
dc.contributor.authorde Almeida, Leonardo Augusto
dc.contributor.authorBelo, Thiago Caetano Andrade
dc.contributor.authorVieira, Fernando Vitor
dc.contributor.authorMohammadi, Nima
dc.contributor.authorKilpeläinen, Petri
dc.contributor.authorGiusti-Paiva, Alexandre
dc.contributor.authorGranato, Daniel
dc.contributor.authorAzevedo, Luciana
dc.contributor.departmentid4100211110
dc.contributor.orcidhttps://orcid.org/0000-0002-0982-0123
dc.contributor.organizationLuonnonvarakeskus
dc.date.accessioned2024-08-05T11:20:16Z
dc.date.accessioned2025-05-28T11:29:29Z
dc.date.available2024-08-05T11:20:16Z
dc.date.issued2024
dc.description.abstractGalactoglucomannan (GGM) is the predominant hemicellulose in coniferous trees, such as Norway spruce, and has been used as a multipurpose emulsifier in the food industry. In vitro digestion with a cellular antioxidant activity assay was performed to determine the bioaccessibility and antioxidant activity of phenolic compounds, and the behaviour of GGM on in vivo experimental assay against induced colon cancer. The results showed that digestion decreased the bioaccessibility and antioxidant capacity of phenolic compounds. Cellular analysis did not support these findings once an antioxidant effect was observed in human cell lines. GGM attenuated the initiation and progression of colon cancer, by reducing the foci of aberrant crypts in rats, and modified the intestinal bacterial microbiota (disrupting the balance between Firmicutes and Bacteroidetes phyla). Thus, GGM provided chemopreventive protection against the development of colon cancer and acted as an intracellular antioxidant agent.
dc.description.vuosik2024
dc.format.bitstreamtrue
dc.format.pagerange12 p.
dc.identifier.olddbid497694
dc.identifier.oldhandle10024/555123
dc.identifier.urihttps://jukuri.luke.fi/handle/11111/22025
dc.identifier.urlhttps://dx.doi.org/10.1016/j.ijbiomac.2024.133986
dc.identifier.urnURN:NBN:fi-fe2024080563745
dc.language.isoen
dc.okm.avoinsaatavuuskytkin1 = Avoimesti saatavilla
dc.okm.corporatecopublicationei
dc.okm.discipline116
dc.okm.internationalcopublicationon
dc.okm.julkaisukanavaoa2 = Osittain avoimessa julkaisukanavassa ilmestynyt julkaisu
dc.okm.selfarchivedon
dc.publisherElsevier
dc.relation.articlenumber133986
dc.relation.doi10.1016/j.ijbiomac.2024.133986
dc.relation.ispartofseriesInternational journal of biological macromolecules
dc.relation.issn0141-8130
dc.relation.issn1879-0003
dc.relation.volume277
dc.rightsCC BY 4.0
dc.source.identifierhttps://jukuri.luke.fi/handle/10024/555123
dc.subjectbioaccessibility
dc.subjecthemicellulose
dc.subjecterythrocytes
dc.teh41007-00282700
dc.titleDigested galactoglucomannan mitigates oxidative stress in human cells, restores gut bacterial diversity, and provides chemopreventive protection against colon cancer in rats
dc.typepublication
dc.type.okmfi=A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä|sv=A1 Originalartikel i en vetenskaplig tidskrift|en=A1 Journal article (refereed), original research|
dc.type.versionfi=Publisher's version|sv=Publisher's version|en=Publisher's version|

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