Journal of Pediatric Gastroenterology and Nutrition · 2009 · 46 citations · 27 references
AgricultureNutritionNutritional SciencesHuman NutritionMaternal NutritionNutritional ToxicologyBreastfeeding NutritionEarly-life NutritionGlutathione MetabolismNeonatal NutritionOxidative Stress PhysiologyPerinatal NutritionArginine NutritionArginine SupplementationBreast Milk Oxidative StressDietary AntioxidantsGlutathione Peroxidase ActivityLipid Peroxidation MarkersMalondialdehyde FormationOxidative Stress Injury
OBJECTIVE: To investigate and compare the effects of enteral glutamine and arginine supply on lipid peroxidation and antioxidant enzyme levels in the small intestine of healthy breast-fed rats. MATERIALS AND METHODS: The study comprised 40 newborn Sprague-Dawley rats born to 5 mother rats. Newborn rats were randomly divided into 4 groups. Starting from day 1 until day 21, group I received only breast milk; group II received breast milk and 200 mg/kg/day oral glutamine; group III received breast milk and 200 mg/kg/day oral arginine; and group IV received breast milk, 200 mg/kg/day glutamine, and 200 mg/kg/day arginine. Malondialdehyde levels and glutathione peroxidase (GPx) and superoxide dismutase activities were measured. RESULTS: The lowest malondialdehyde levels were found in group II (P = 0.0001). Superoxide dismutase activity was found to be significantly higher in group II than group I (P < 0.001). Of the 4 groups, GPx activity was highest in group IV. GPx activity in group II was significantly higher than in group I (P = 0.001) or group III (P = 0.001). GPx activity was higher in group IV than in group I (P = 0.001) or group III (P = 0.001). CONCLUSIONS: Enteral glutamine alone or in the presence of arginine has favorable effects on oxidative stress not only in experimental models of hypoxia-reoxygenation, but also in healthy newborn rats. This suggests that in premature neonates with insufficient oxidative resistance, glutamine and arginine supplementation may help prevent necrotizing enterocolitis.
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A simple method for clinical assay of superoxide dismutase.
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Improved fluorometric determination of malonaldehyde
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