<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-29T07:01:01Z</responseDate><request verb="GetRecord" identifier="oai:riubu.ubu.es:10259/8069" metadataPrefix="marc">https://riubu.ubu.es/oai/request</request><GetRecord><record><header><identifier>oai:riubu.ubu.es:10259/8069</identifier><datestamp>2023-11-22T01:05:28Z</datestamp><setSpec>com_10259_5827</setSpec><setSpec>com_10259_5086</setSpec><setSpec>com_10259_2604</setSpec><setSpec>col_10259_5828</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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<subfield code="a">Durán Fernández-Feijóo, Cristina</subfield>
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<subfield code="a">Rodríguez-Fanjul, Javier</subfield>
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<subfield code="a">López-Abat, Miriam</subfield>
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<subfield code="a">Hadley, Stephanie</subfield>
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<subfield code="a">Cavia Saiz, Mónica</subfield>
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<subfield code="a">Muñiz Rodríguez, Pilar</subfield>
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<subfield code="a">Arnaez, Juan</subfield>
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<subfield code="a">Fernández-Lorenzo, José Ramón</subfield>
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<subfield code="a">Camprubí Camprubí, Marta</subfield>
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<subfield code="a">Hypoxic ischemic encephalopathy (HIE) is one of the main causes of morbidity and mortality during the neonatal period, despite treatment with hypothermia. There is evidence that oxidative&#xd;
damage plays an important role in the pathophysiology of hypoxic-ischemic (HI) brain injury. Our&#xd;
aim was to investigate whether postnatal allopurinol administration in combination with hypothermia would reduce oxidative stress (OS) biomarkers in an animal model of HIE. Postnatal 10-day rat&#xd;
pups underwent unilateral HI of moderate severity. Pups were randomized into: Sham operated,&#xd;
hypoxic-ischemic (HI), HI + allopurinol (HIA), HI + hypothermia (HIH), and HI + hypothermia&#xd;
+ allopurinol (HIHA). Biomarkers of OS and antioxidants were evaluated: GSH/GSSG ratio and&#xd;
carbonyl groups were tested in plasma. Total antioxidant capacity (TAC) was analyzed in plasma and&#xd;
cerebrospinal fluid, and 8-iso-prostaglandin F2α was measured in brain tissue. Plasma 2,20–azinobis-&#xd;
(3-ethyl-benzothiazoline-6-sulfonic acid) (ABTS) levels were preserved in those groups that received&#xd;
allopurinol and dual therapy. In cerebrospinal fluid, only the HIA group presented normal ferric&#xd;
reducing ability of plasma (FRAP) levels. Protein oxidation and lipid peroxidation were significantly&#xd;
reduced in all groups treated with hypothermia and allopurinol, thus enhancing neuroprotection&#xd;
in HIE.</subfield>
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<subfield code="a">http://hdl.handle.net/10259/8069</subfield>
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<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">10.3390/antiox10101523</subfield>
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<datafield tag="024" ind2=" " ind1="8">
<subfield code="a">2076-3921</subfield>
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<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Allopurinol</subfield>
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<subfield code="a">Hypothermia</subfield>
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<subfield code="a">Hypoxic-ischemic encephalopathy</subfield>
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<subfield code="a">Oxidative stress</subfield>
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<datafield ind1=" " ind2=" " tag="653">
<subfield code="a">Oxidative damage</subfield>
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<datafield tag="245" ind1="0" ind2="0">
<subfield code="a">Effects of Hypothermia and Allopurinol on Oxidative Status in a Rat Model of Hypoxic Ischemic Encephalopathy</subfield>
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