Prolonging in utero-like oxygenation after birth diminishes oxidative stress in the lung and brain of mice pups☆
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Prolonging in utero-like oxygenation after birth diminishes oxidative stress in the lung and brain of mice pups☆

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Prolonging in utero-like oxygenation after birth diminishes oxidative stress in the lung and brain of mice pups☆

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dc.contributor.author Escobar, Javier es_ES
dc.contributor.author Cubells, Elena es_ES
dc.contributor.author Enomoto, Masahiro es_ES
dc.contributor.author Quintás Alonso, Guillermo es_ES
dc.contributor.author Kuligowski, Julia es_ES
dc.contributor.author Martínez Fernández, Cristina es_ES
dc.contributor.author Torres-Cuevas, Isabel es_ES
dc.contributor.author Sastre, Juan es_ES
dc.contributor.author Belik, Jaques es_ES
dc.contributor.author Vento Torres, Máximo es_ES
dc.date.accessioned 2015-06-19T07:47:46Z
dc.date.available 2015-06-19T07:47:46Z
dc.date.issued 2013 es_ES
dc.identifier.citation Redox Biology Vol. 1 Issue 1: pp. 297-303 es_ES
dc.identifier.uri http://hdl.handle.net/10550/44511
dc.description.abstract BackgroundFetal-to-neonatal transition is associated with oxidative stress. In preterm infants, immaturity of the antioxidant system favours supplemental oxygen-derived morbidity and mortality.ObjectivesTo assess if prolonging in utero-like oxygenation during the fetal-to-neonatal transition limits oxidative stress in the lung and brain, improving postnatal adaptation of mice pups.Material and methodsInspiratory oxygen fraction (FiO2) in pregnant mice was reduced from 21% (room air) to 14% (hypoxia) 8–12 h prior to delivery and reset to 21% 6–8 h after birth. The control group was kept at 21% during the procedure. Reduced (GSH) and oxidized (GSSG) glutathione and its precursors [γ-glutamyl cysteine (γ-GC) and L-cysteine (CySH)] content and expression of several redox-sensitive genes were evaluated in newborn lung and brain tissue 1 (P1) and 7 (P7) days after birth.ResultsAs compared with control animals, the GSH/GSSG ratio was increased in the hypoxic group at P1 and P7 in the lung, and at P7 in the brain. In the hypoxic group a significant increase in the mRNA levels of NAD(P)H:quinone oxidoreductase 1 (noq1), Sulfiredoxin 1 (srnx1) and Glutathione Peroxidase 1 (gpx) was found in lung tissue at P1, as well as a significant increase in gpx in brain tissue at P7.ConclusionsDelaying the increase in tissue oxygenation to occur after birth reduces short-and-long-term oxidative stress in the lung. Similar yet more subtle effects were found in the brain. Apparently, the fetal-to-neonatal transition under hypoxic conditions appears to have protective qualities. es_ES
dc.subject CySH (l-cysteine) es_ES
dc.subject CyS–NEM (cysteine covalently bonded to N-ethylmaleimide) es_ES
dc.subject FiO2 (inspiratory oxygen fraction) es_ES
dc.subject gapdh (glyceraldehyde-3-phosphate dehydrogenase gene) es_ES
dc.subject GCL (glutamylcysteine ligase) es_ES
dc.subject gclm (glutamylcysteine ligase modifier subunit gene) es_ES
dc.subject γ-GC (gamma-glutamyl cysteine) es_ES
dc.subject γ-GC–NEM (gamma-glutamyl cysteine covalently bonded to N-ethylmaleimide) es_ES
dc.subject gpx1 (glutathione peroxidase 1 gene) es_ES
dc.subject GSH (reduced glutathione) es_ES
dc.subject GS–NEM (reduced glutathione covalently bonded to N-ethylmaleimide) es_ES
dc.subject gsr (glutathione reductase gene) es_ES
dc.subject GSSG (oxidized glutathione) es_ES
dc.subject G18 (18th day of gestation) es_ES
dc.subject g6pdx (glucose 6 phosphate dehydrogenase gene) es_ES
dc.subject LC–MS/MS (liquid chromatography coupled to tandem mass spectrometry) es_ES
dc.subject m/z (mass-to-charge ratio) es_ES
dc.subject noq1 (NAD(P)H:quinone oxidoreductase 1) es_ES
dc.subject me1 (malic enzyme 1 gene) es_ES
dc.subject NEM (N-ethylmaleimide) es_ES
dc.subject O14 (hypoxia group FiO2=14%) es_ES
dc.subject O21 (normoxia group FiO2=21%) es_ES
dc.subject paO2 (partial pressure of oxygen) es_ES
dc.subject pgd (phosphogluconate dehydrogenase gene) es_ES
dc.subject P1 (24 h after birth) es_ES
dc.subject P7 (1 week after birth) es_ES
dc.subject SpO2 (oxygen saturation) es_ES
dc.subject srnx1 (sulfiredoxin 1 gene) es_ES
dc.subject trxnd1 (thioredoxin reductase 1 gene) es_ES
dc.subject fetal-to-neonatal transition es_ES
dc.subject oxygen es_ES
dc.subject oxidative stress es_ES
dc.subject redox regulation es_ES
dc.subject glutathione es_ES
dc.title Prolonging in utero-like oxygenation after birth diminishes oxidative stress in the lung and brain of mice pups☆ es_ES
dc.type journal article es_ES
dc.identifier.doi 10.1016/j.redox.2013.04.002 es_ES
dc.identifier.idgrec 097581 es_ES

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