Antioxidants 2019
DOI: 10.5772/intechopen.85175
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Antioxidants at Newborns

Abstract: Humans possess defense mechanisms against free radicals: enzymatic and nonenzymatic antioxidants. Antioxidant defense is deficient in newborns and can be enhanced by the action of reactive oxygen species, generated by perinatal diseases such as respiratory distress or asphyxia. Prematurity itself will be associated with deficient antioxidant mechanisms, which are primarily enzymatic, but also nonenzymatic. Under oxidative stress conditions, antioxidant defense is overcome and thus, low-molecular weight free ir… Show more

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Cited by 6 publications
(5 citation statements)
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“…However, the upregulation of HO-1 will also cause Fe deposition in the brain, which worsens and accelerates disease progression by enhancing the redox imbalance in ongoing AD lesions [49,[124][125][126] . It should be recalled that the brain possesses very low antioxidant capacity compared to other organs, being much lower in neonatal life [127,128] and in the elderly [129,130] . Thus, the enhanced pro-oxidant milieu due to HO-1 hyperactivation leads to an increased oxidative and nitrosative post-translational modification of cellular enzymes, with their consequent inactivation [131] .…”
Section: Admentioning
confidence: 99%
“…However, the upregulation of HO-1 will also cause Fe deposition in the brain, which worsens and accelerates disease progression by enhancing the redox imbalance in ongoing AD lesions [49,[124][125][126] . It should be recalled that the brain possesses very low antioxidant capacity compared to other organs, being much lower in neonatal life [127,128] and in the elderly [129,130] . Thus, the enhanced pro-oxidant milieu due to HO-1 hyperactivation leads to an increased oxidative and nitrosative post-translational modification of cellular enzymes, with their consequent inactivation [131] .…”
Section: Admentioning
confidence: 99%
“…It is known that immaturity and reduced adaptive mechanisms in preterm infants are depleted, starting as early as intrauterine, during birth and in the postnatal period of life, due to stress factors such as hypoxia, hyperoxia, reperfusion and inflammation [16]. For a deeper understanding of these processes, we performed a clinical and morphological comparison of the functional and structural features of the pineal gland of the brain in early infants with ELBW.…”
Section: Resultsmentioning
confidence: 99%
“…Also an inflammatory reaction develops in response to lung tissue damage by oxygen, and elevated levels of pro-inflammatory cytokines are found in higher concentrations in children who develop chronic lung diseases ( 16 , 17 ). Some authors also suggest that lung damage in BPD is associated not only with the influence of active oxygen radicals, but with a decrease in antioxidant activity and the insufficient protective functions in preterm neonates ( 12 , 18 ). As shown in our results, the sensitivity and specificity of the ROC curve analysis were quite high (80% and 64%, respectively), indicating that low urinary melatonin concentrations in the early neonatal period could predict the development of BPD with high reliability.…”
Section: Discussionmentioning
confidence: 99%