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Published on: November 20, 2015
The precarious antioxidant defenses of the preterm infant
1Department of Pediatrics, Children's Mercy Hospital and The University of Missouri-Kansas City School of Medicine, 64108, USA.
Insights
Preterm infants are vulnerable to illnesses caused by oxygen radicals due to immature antioxidant defenses. This review explores oxidant sources, defenses, and antioxidant therapies for preterm infants.
Area of Science:
- Neonatal Medicine
- Biochemistry
- Pediatric Oxidative Stress
Background:
- Oxygen radicals are implicated in numerous preterm infant illnesses.
- Immature antioxidant systems in preterm infants increase susceptibility to oxidative damage.
- Understanding these vulnerabilities is crucial for developing effective treatments.
Purpose of the Study:
- To review antioxidant defenses in immature animals and preterm infants.
- To quantify infant vulnerabilities to oxidants.
- To explore oxidant sources and their impact on developing antioxidant systems.
Main Methods:
- Review of literature on antioxidant defenses and oxidant sources.
- Analysis of genetic manipulation models (knockout/transgenic mice) for antioxidant enzymes.
- Exploration of clinical and investigational antioxidant therapies.
Main Results:
- Identified key sources of oxidants affecting preterm infants, including hyperoxia and iron.
- Discussed the impact of these oxidants on immature antioxidant enzyme activity.
- Reviewed genetic models demonstrating the role of antioxidant enzymes.
Conclusions:
- Preterm infants possess vulnerable antioxidant defenses susceptible to various oxidants.
- Genetic manipulation studies provide insights into antioxidant enzyme function.
- Challenges exist in designing and implementing effective antioxidant therapies for preterm infants.
Abstract:
Oxygen radicals are considered to be major causative factors in many illnesses of preterm infants. This article reviews the antioxidant defenses in immature animals and preterm infants, and attempts to quantitate their vulnerabilities to oxidants. Sources of oxidants, including hyperoxia, iron, parenteral nutrition, nitric oxide, and prooxidants, and their impact on immature antioxidant defenses are discussed. Genetic manipulations of antioxidant enzymes such as knockout and transgenic mice models are reviewed. The various clinical and investigational antioxidant therapies in animals and humans and difficulties in the design of antioxidant therapy studies are explored.
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