Publication:
Epicatechin modulates stress-resistance in C. elegans via insulin/IGF-1 signaling pathway.

dc.contributor.authorAyuda-Durán, Begoña
dc.contributor.authorGonzález-Manzano, Susana
dc.contributor.authorMiranda-Vizuete, Antonio
dc.contributor.authorDueñas, Montserrat
dc.contributor.authorSantos-Buelga, Celestino
dc.contributor.authorGonzález-Paramás, Ana M
dc.date.accessioned2023-01-25T10:29:06Z
dc.date.available2023-01-25T10:29:06Z
dc.date.issued2019-01-28
dc.description.abstractThe nematode Caenorhabditis elegans has been used to examine the influence of epicatechin (EC), an abundant flavonoid in the human diet, in some stress biomarkers (ROS production, lipid peroxidation and protein carbonylation). Furthermore, the ability of EC to modulate the expression of some key genes in the insulin/IGF-1 signaling pathway (IIS), involved in longevity and oxidative or heat shock stress response, has also been explored. The final aim was to contribute to the elucidation of the mechanisms involved in the biological effects of flavonoids. The results showed that EC-treated wild-type C. elegans exhibited increased survival and reduced oxidative damage of biomolecules when submitted to thermal stress. EC treatment led to a moderate elevation in ROS levels, which might activate endogenous mechanisms of defense protecting against oxidative insult. The enhanced stress resistance induced by EC was found to be mediated through the IIS pathway, since assays in daf-2, age-1, akt-1, akt-2, sgk-1, daf-16, skn-1 and hsf-1 loss of function mutant strains failed to show any heat-resistant phenotype against thermal stress when treated with EC. Consistently, EC treatment upregulated the expression of some stress resistance associated genes, such as gst-4, hsp-16.2 and hsp-70, which are downstream regulated by the IIS pathway.
dc.identifier.doi10.1371/journal.pone.0199483
dc.identifier.essn1932-6203
dc.identifier.pmcPMC6349306
dc.identifier.pmid30689636
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349306/pdf
dc.identifier.unpaywallURLhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0199483&type=printable
dc.identifier.urihttp://hdl.handle.net/10668/13471
dc.issue.number1
dc.journal.titlePloS one
dc.journal.titleabbreviationPLoS One
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.numbere0199483
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAnimals
dc.subject.meshCaenorhabditis elegans
dc.subject.meshCaenorhabditis elegans Proteins
dc.subject.meshCatechin
dc.subject.meshInsulin
dc.subject.meshInsulin-Like Growth Factor I
dc.subject.meshLipid Peroxidation
dc.subject.meshOxidative Stress
dc.subject.meshReactive Oxygen Species
dc.subject.meshSignal Transduction
dc.titleEpicatechin modulates stress-resistance in C. elegans via insulin/IGF-1 signaling pathway.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number14
dspace.entity.typePublication

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