Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update
Preterm newborns are challenged by an excessive oxidative burden, as a result of several perinatal stimuli, as intrauterine infections, resuscitation, mechanical ventilation, and postnatal complications, in the presence of immature antioxidant capacities. “Oxygen radical disease of neonatology” comp...
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Series: | Oxidative Medicine and Cellular Longevity |
Online Access: | http://dx.doi.org/10.1155/2014/721043 |
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doaj-e75e2e7b65d84bbd82e165237c80f5e02020-11-24T23:17:10ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942014-01-01201410.1155/2014/721043721043Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An UpdateChiara Poggi0Carlo Dani1Neonatal Intensive Care Unit, Careggi University Hospital, 3 Largo Brambilla, 50141 Florence, ItalySection of Neonatology, Department of Neurosciences, Psychology, Drug Research and Child Health, Careggi University Hospital, 3 Largo Brambilla, 50141 Florence, ItalyPreterm newborns are challenged by an excessive oxidative burden, as a result of several perinatal stimuli, as intrauterine infections, resuscitation, mechanical ventilation, and postnatal complications, in the presence of immature antioxidant capacities. “Oxygen radical disease of neonatology” comprises a wide range of conditions sharing a common pathway of pathogenesis and includes bronchopulmonary dysplasia (BPD) and other main complications of prematurity. Antioxidant strategies may be beneficial in the prevention and treatment of oxidative stress- (OS-) related lung disease of the preterm newborn. Endotracheal supplementation or lung-targeted overexpression of superoxide dismutase was proved to reduce lung damage in several models; however, the supplementation in preterm newborn failed to reduce the risk of BPD, although long-term respiratory outcomes were improved. Also melatonin administration to small cohorts of preterm newborns suggested beneficial effects on lung OS. The possibility to identify single nucleotide polymorphism affecting the risk of BPD may help to identify specific populations with particularly high risk of OS-related diseases and may pose the basis for individually targeted treatments. Finally, surfactant replacement may lead to local anti-inflammatory and antioxidant effects, thanks to specific enzymatic and nonenzymatic antioxidants naturally present in animal surfactants.http://dx.doi.org/10.1155/2014/721043 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chiara Poggi Carlo Dani |
spellingShingle |
Chiara Poggi Carlo Dani Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update Oxidative Medicine and Cellular Longevity |
author_facet |
Chiara Poggi Carlo Dani |
author_sort |
Chiara Poggi |
title |
Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update |
title_short |
Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update |
title_full |
Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update |
title_fullStr |
Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update |
title_full_unstemmed |
Antioxidant Strategies and Respiratory Disease of the Preterm Newborn: An Update |
title_sort |
antioxidant strategies and respiratory disease of the preterm newborn: an update |
publisher |
Hindawi Limited |
series |
Oxidative Medicine and Cellular Longevity |
issn |
1942-0900 1942-0994 |
publishDate |
2014-01-01 |
description |
Preterm newborns are challenged by an excessive oxidative burden, as a result of several perinatal stimuli, as intrauterine infections, resuscitation, mechanical ventilation, and postnatal complications, in the presence of immature antioxidant capacities. “Oxygen radical disease of neonatology” comprises a wide range of conditions sharing a common pathway of pathogenesis and includes bronchopulmonary dysplasia (BPD) and other main complications of prematurity. Antioxidant strategies may be beneficial in the prevention and treatment of oxidative stress- (OS-) related lung disease of the preterm newborn. Endotracheal supplementation or lung-targeted overexpression of superoxide dismutase was proved to reduce lung damage in several models; however, the supplementation in preterm newborn failed to reduce the risk of BPD, although long-term respiratory outcomes were improved. Also melatonin administration to small cohorts of preterm newborns suggested beneficial effects on lung OS. The possibility to identify single nucleotide polymorphism affecting the risk of BPD may help to identify specific populations with particularly high risk of OS-related diseases and may pose the basis for individually targeted treatments. Finally, surfactant replacement may lead to local anti-inflammatory and antioxidant effects, thanks to specific enzymatic and nonenzymatic antioxidants naturally present in animal surfactants. |
url |
http://dx.doi.org/10.1155/2014/721043 |
work_keys_str_mv |
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