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dc.contributor.authorSaera-Vila, Alfonso-
dc.contributor.authorCalduch-Giner, Josep A.-
dc.contributor.authorPrunet, Patrick-
dc.contributor.authorPérez-Sánchez, Jaume-
dc.date.accessioned2012-03-02T13:18:21Z-
dc.date.available2012-03-02T13:18:21Z-
dc.date.issued2009-10-
dc.identifier.citationComparative biochemistry and physiology, Part A, Molecular & integrative physiology 154(2): 197-203 (2009)es_ES
dc.identifier.issn1095-6433-
dc.identifier.urihttp://hdl.handle.net/10261/46544-
dc.description32 p., 1 tabla, 5 figuras y bibliografíaes_ES
dc.description.abstractThe time courses of liver GH/IGF axis and selected stress markers were analyzed in juvenile gilthead sea bream (Sparus aurata) sampled at zero time and at fixed intervals (1.5, 3, 6, 24, 72 and 120 h) after acute confinement (120 kg/m3). Fish remained unfed throughout the course of the confinement study, and the fasting-induced increases in plasma growth hormone (GH) levels were partially masked by the GH-stress inhibitory tone. Hepatic mRNA levels of growth hormone receptor-I (GHR-I) were not significantly altered by confinement, but a persistent 2-fold decrease in GHR-II transcripts was found at 24 and 120 h. A consistent decrease in circulating levels of insulin-like growth factor-I (IGF-I) was also found through most of the experimental period, and the down-regulated expression of GHR-II was positively correlated with changes in hepatic IGF-I and IGF-II transcripts. This stress-specific response was concurrent with plasma increases in cortisol and glucose levels, reflecting the cortisol peak (60-70 ng/mL), the intensity and duration of the stressor when data found in the literature were compared. Adaptive responses against oxidative damage were also found, and a rapid enhanced expression was reported in the liver tissue for mitochondrial heat-shock proteins (glucose regulated protein 75). At the same time, the down-regulated expression of proinflammatory cytokines (tumour necrosis factor-α) and detoxifying enzymes (cytochrome P450 1A1) might dictate the hepatic depletion of potential sources of reactive oxygen species. These results provide suitable evidence for a functional partitioning of hepatic GHRs under states of reduced IGF production and changing cellular environment resulting from acute confinement.es_ES
dc.description.sponsorshipThis work was funded by EU (contract no. SSP98-CT-2004-513692; Combined genetic and functional genomic approaches for stress and disease resistance markers assisted selection in fish and shellfish, AQUAFIRST) and Spanish (Ingenio-2010 Programme; Improvement of Aquaculture Production by the use of biotechnological tools, AQUAGENOMICS) projects. AS-V was recipient of a Spanish PhD fellowship from the Diputación Provincial de Castellón.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsopenAccesses_ES
dc.subjectCortisoles_ES
dc.subjectGlucose regulated protein 75es_ES
dc.subjectTumour necrosis factor-αes_ES
dc.subjectCytochrome P450 1A1es_ES
dc.titleDynamics of liver GH/IGF axis and selected stress markers in juvenile gilthead sea bream (Sparus aurata) exposed to acute confinement. Differential stress response of growth hormone receptorses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/j.cbpa.2009.06.004-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.cbpa.2009.06.004es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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