Abstract:OBJECTIVE: To study the effect of melatonin, a potent antioxidant both in vitro and in vivo, on hyperoxia-induced oxidant/antioxidant imbalance in the lung of neonatal rats with chronic lung disease (CLD). METHODS: Ninety neonatal rats were randomly divided into three groups (n=30 each): air-exposed, hyperoxia-exposed, melatonin-treated (4 mg/kg melatonin was administered 30 minutes before hyperoxia exposure and once daily after exposure). CLD was induced by hyperoxia exposure (FiO2=0.85). Lung specimens were obtained 3, 7, and 14 days after exposure (n=10 each) for histopathologic examination. The levels of total antioxidase capacity (T-AOC), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), myeloperoxidase (MPO), catalase (CAT), nitrite/nitrate, and malondialdehyde (MDA) in the lung were assayed by the spectrophotometer. RESULTS: The histopathologic examination showed that lung damage was obviously alleviated in the melatonin-treated group. The levels of T-AOC, GSH-Px, SOD and CAT in the lung were significantly higher in the melatonin-treated group than those in the other two groups at all time points (P<0.05). The levels of MPO, nitrite/nitrate and MDA in the lung increased significantly in the untreated hypoxia-exposed group compared with those in the air-exposed group at all time points (P<0.05 or 0.01), while the levels of MPO, nitrite/nitrate and MDA in the melatonin-treated group were significantly reduced as compared with the untreated hypoxia-exposed group (P<0.05). CONCLUSIONS: Melatonin may reverse oxidant/antioxidant imbalance in hyperoxia-induced lung disease, thus providing a protective effect against CLD in neonatal rats.[Chin J Contemp Pediatr, 2009, 11 (7):581-584]
PAN Li,XU Wei,FU Jian-Hua et al. Effect of melatonin on hyperoxia-induced oxidant/antioxidant imbalance in the lung of neonatal rats with chronic lung disease[J]. CJCP, 2009, 11(07): 581-584.
[1]Asikainen TM, White CW. Pulmonary antioxidant defenses in the preterm newborn with respiratory distress and bronchopulmonary dysplasia in evolution: implications for antioxidant therapy[J]. Antioxid Redox Signal, 2004, 6(1):155-167.
[2]Reiter RJ. Oxidative damage in the central nervous system: protection by melatonin [J]. Prog Neurobiol, 1998, 56(3):359-384.
[3]Gitto E, Reiter RJ, Sabatino G, Buonocore G, Romeo C, Gitto P, et al. Correlation among cytokines, bronchopulmonary dysplasia and modality of ventilation in preterm newborns: improvement with melatonin treatment [J]. J Pineal Res, 2005, 39(3):287-293.
[5]Ogihara T, Hirano K, Morinobu T, Kim HS, Hiroi M, Ogihara H, et al. Raised concentration of aldehyde lipid peroxidation products in premature infants with chronic lung disease[J]. Arch Dis Child Fetal Neonatal Ed, 1999, 80(1):F21-F25.
[6]Kaarteenaho-Wiik R, Kinnula VL. Distribution of antioxidant enzymes in developing human lung, respiratory distress syndrome, and bronchopulmonary dysplasia[J]. J Histochem Cytochem, 2004, 52(9):1231-1240.
[7]Asikainen TM, Raivio KO, Saksela M, Kinnula VL. Expression and developmental profile of antioxidant enzymes in human lung and liver [J]. Am J Respir Cell Mol Biol, 1998, 19(6):942-949.
[8]Dani C, Cecchi A, Bertini G. Role of oxidative stress as physiopathologic factor in the preterm infant[J]. Minerva Pediatr, 2004, 56(4):381-394.
[9]Tan DX, Manchester LC, Terron MP, Flores LJ, Reiter RJ. One molecule, many derivatives: a never-ending interaction of melatonin with reactive oxygen and nitrogen species?[J]. J Pineal Res, 2007, 42(1):28-42.
[10]Bandyopadhyay D, Biswas K, Bandyopadhyay U, Reiter RJ, Banerjee RK. Melatonin protects against stress-induced gastric lesions by scavenging the hydroxyl radical[J]. J Pineal Res, 2000, 29(3):143-151.
[11]Rodriguez C, Mayo JC, Sainz RM, Antolín I, Herrera F, Martín V, et al. Regulation of antioxidant enzymes: a significant role for melatonin[J]. J Pineal Res, 2004, 36(1):1-9.
[12]Giacomo CG, Antonio M. Melatonin in cardiac ischemia/reperfusion-induced mitochondrial adaptive changes [J]. Cardiovasc Hematol Disord Drug Targets, 2007, 7(3):163-169.
[13]Maharaj DS, Glass BD, Daya S. Melatonin: new places in therapy[J]. Biosci Rep, 2007, 27(6):299-320.
[16]Jahnke G, Marr M, Myers C, Wilson R, Travlos G, Price C. Maternal and developmental toxicity evaluation of melatonin administration orally to pregnant Sprague-Dawley rats[J]. Toxicol Res, 1999, 50(2):271-279.