Oxidative attack during temperature fluctuation challenge compromises liver protein homeostasis of a temperate fish model

dc.contributor.authorSánchez Nuño, Sergio
dc.contributor.authorSanahuja Piera, Ignasi
dc.contributor.authorFernández-Alacid, Laura
dc.contributor.authorOrdóñez-Grande, Borja
dc.contributor.authorCarbonell i Camós, Teresa
dc.contributor.authorIbarz i Valls, Antoni
dc.date.accessioned2019-09-27T13:59:01Z
dc.date.available2020-07-04T05:10:29Z
dc.date.issued2019-07-04
dc.date.updated2019-09-27T13:59:01Z
dc.description.abstractSeasonal variations in water temperature are a natural stressor of temperate fish that affect growth performance and metabolism globally. Gilthead sea bream is one of the most economically interesting species in the Mediterranean; but its liver metabolism is affected by the cold season. However, the effects of cold on protein turnover mechanisms have hardly been studied. Here, we study the relationship between liver oxidative status and protein homeostasis pathways during a 50-day low temperature period at 14 °C, and subsequent recovery at two times: 7 days (early recovery) and 30 days (late recovery). Liver redox status was determined by measuring oxidised lipids and proteins, the glutathione redox cycle and major antioxidant enzymes activities. Protein turnover was analysed via liver protein expression of HSP70 and HSP90; proteasome 26S subunits and polyubiquitination, as markers of the ubiquitin-proteasome system (UPS); and cathepsin D, as a lysosomal protease. Low temperature exposure depressed antioxidant enzyme activities, affecting the glutathione redox cycle and reducing total glutathione levels. Both the UPS and lysosomal pathways were also depressed and consequently, oxidised protein accumulated in liver. Interestingly, both protein oxidation and polyubiquitination tagging depended on protein molecular weight. Despite all these alterations, temperature recovery reverted most consequences of the cold at different rates: with delayed recovery of total glutathione levels and oxidised protein degradation with respect to enzyme activities recovery. All these findings demonstrate that protein liver homeostasis is compromised after chronic cold exposure and could be the cause of liver affectations reported in aquaculture of temperate fish.
dc.format.extent11 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec691598
dc.identifier.issn1096-4959
dc.identifier.urihttps://hdl.handle.net/2445/141105
dc.language.isoeng
dc.publisherElsevier Ltd
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.cbpb.2019.110311
dc.relation.ispartofComparative Biochemistry and Physiology B-Biochemistry & Molecular Biology, 2019, vol. 236, p. 110311
dc.relation.urihttps://doi.org/10.1016/j.cbpb.2019.110311
dc.rightscc-by-nc-nd (c) Elsevier Ltd, 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)
dc.subject.classificationPeixos marins
dc.subject.classificationProteïnes
dc.subject.classificationTemperatura
dc.subject.otherMarine fishes
dc.subject.otherProteins
dc.subject.otherTemperature
dc.titleOxidative attack during temperature fluctuation challenge compromises liver protein homeostasis of a temperate fish model
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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