Environmental Enrichment Modified Epigenetic Mechanisms in SAMP8 Mouse Hippocampus by Reducing Oxidative Stress and Inflammaging and Achieving Neuroprotection

dc.contributor.authorGriñán Ferré, Christian
dc.contributor.authorPuigoriol Illamola, Dolors
dc.contributor.authorPalomera Ávalos, Verónica
dc.contributor.authorPérez Cáceres, David
dc.contributor.authorCompanys Alemany, Júlia
dc.contributor.authorCamins Espuny, Antoni
dc.contributor.authorOrtuño Sahagún, Daniel
dc.contributor.authorRodrigo i Calduch, Ma. Teresa
dc.contributor.authorPallàs i Llibería, Mercè, 1964-
dc.date.accessioned2019-11-26T12:36:18Z
dc.date.available2019-11-26T12:36:18Z
dc.date.issued2016-06-18
dc.date.updated2019-11-26T12:36:18Z
dc.description.abstractWith the increase in life expectancy, aging and age-related cognitive impairments arebecoming one of the most important issues for human health. At the same time, ithas been shown that epigenetic mechanisms are emerging as universally importantfactors in life expectancy. The Senescence Accelerated Mouse P8 (SAMP8) strainexhibits age-related deterioration evidenced in learning and memory abilities and is auseful model of neurodegenerative disease. In SAMP8, Environmental Enrichment (EE)increased DNA-methylation levels (5-mC) and reduced hydroxymethylation levels (5-hmC), as well as increased histone H3 and H4 acetylation levels. Likewise, we foundchanges in the hippocampal gene expression of some chromatin-modifying enzymegenes, such asDnmt3b,Hdac1,Hdac2,Sirt2, andSirt6.Subsequently, we assessedthe effects of EE on neuroprotection-related transcription factors, such as the Nuclearregulatory factor 2 (Nrf2)-Antioxidant Response Element pathway and Nuclear Factorkappa Beta (NF-κB), which play critical roles in inflammation. We found that EE producesan increased expression of antioxidant genes, such asHmox1,Aox1, andCox2, andreduced the expression of inflammatory genes such asIL-6andCxcl10, all of this withinthe epigenetic context modified by EE. In conclusion, EE prevents epigenetic changesthat promote or drive oxidative stress and inflammaging
dc.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec680650
dc.identifier.issn1663-4365
dc.identifier.pmid27803663
dc.identifier.urihttps://hdl.handle.net/2445/145413
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fnagi.2016.00241
dc.relation.ispartofFrontiers in Aging Neuroscience, 2016, vol. 8, num. 241
dc.relation.urihttps://doi.org/10.3389/fnagi.2016.00241
dc.rightscc-by (c) Griñan Ferré, Christian et al., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject.classificationEpigenètica
dc.subject.classificationEstrès oxidatiu
dc.subject.classificationInflamació
dc.subject.classificationMalalties neurodegeneratives
dc.subject.otherEpigenetics
dc.subject.otherOxidative stress
dc.subject.otherInflammation
dc.subject.otherNeurodegenerative Diseases
dc.titleEnvironmental Enrichment Modified Epigenetic Mechanisms in SAMP8 Mouse Hippocampus by Reducing Oxidative Stress and Inflammaging and Achieving Neuroprotection
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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