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<field name="value">Durán Fernández-Feijóo, Cristina</field>
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<field name="value">Rodríguez-Fanjul, Javier</field>
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<field name="value">López-Abat, Miriam</field>
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<field name="value">Hadley, Stephanie</field>
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<field name="value">Cavia Saiz, Mónica</field>
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<field name="value">Muñiz Rodríguez, Pilar</field>
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<field name="value">Arnaez, Juan</field>
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<field name="value">Fernández-Lorenzo, José Ramón</field>
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<field name="value">Camprubí Camprubí, Marta</field>
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<field name="value">2023-11-21T08:12:55Z</field>
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<field name="value">2021-09</field>
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<field name="value">http://hdl.handle.net/10259/8069</field>
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<field name="value">10.3390/antiox10101523</field>
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<field name="value">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.</field>
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<field name="value">eng</field>
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<field name="value">Antioxidants. 2021, V. 10, n. 10, 1523</field>
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<field name="value">https://doi.org/10.3390/antiox10101523</field>
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<field name="value">Atribución 4.0 Internacional</field>
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<field name="value">Allopurinol</field>
<field name="value">Hypothermia</field>
<field name="value">Hypoxic-ischemic encephalopathy</field>
<field name="value">Oxidative stress</field>
<field name="value">Oxidative damage</field>
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<field name="value">Bioquímica</field>
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<field name="value">Effects of Hypothermia and Allopurinol on Oxidative Status in a Rat Model of Hypoxic Ischemic Encephalopathy</field>
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<field name="value">10</field>
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