F 2-isoprostanes, prostaglandin F 2-like compounds formed by free radical-catalyzed lipid peroxidation, are considered the most reliable markers of oxidative stress. It has been repeatedly suggested that newborns are exposed to conditions of oxidative stress resulting from the change from a low oxygen pressure in utero to a high oxygen pressure at birth. We measured the levels of F 2-isoprostanes in plasma of newborns by gas chromatography/mass spectrometry and we found that F 2-isoprostanes are significantly higher in term newborns compared to healthy adults. The greatest values were found in preterm newborns in whom F 2- isoprostanes are even higher than in term babies. Moreover a significant inverse correlation was found between the plasma levels of isoprostanes and the gestational age. A quite normal level of isoprostanes was found in the mothers both at delivery and during pregnancy. Placental total F 2- isoprostanes (sum of free plus esterified) were significantly higher in preterm compared to term deliveries and such a difference might account for the difference in plasma isoprostanes. Plasma non-protein-bound iron is higher in preterm than in term newborns, even if no correlation was found with plasma F 2-isoprostanes. Erythrocyte desferrioxamine-chelatable iron content (0 time) and release (24 h of aerobic incubation) are higher in newborns than in adults and in preterm than in term newborns, but again no correlation was found with plasma F 2-isoprostanes. The marked increase in plasma isoprostanes suggests that oxidative stress is a feature of the physiopathological changes seen in the perinatal period. © 2004 Elsevier Inc. All rights reserved.

Comporti, M., Signorini, C., Leoncini, S., Buonocore, G., Rossi, V., Ciccoli, L. (2004). Plasma F2-isoprostanes are elevated in newborns and inversely correlated to gestational age. FREE RADICAL BIOLOGY & MEDICINE, 37(5), 724-732 [10.1016/j.freeradbiomed.2004.06.007].

Plasma F2-isoprostanes are elevated in newborns and inversely correlated to gestational age

Comporti, M.;Signorini, C.;Leoncini, S.;Buonocore, G.;Rossi, V.;Ciccoli, L.
2004-01-01

Abstract

F 2-isoprostanes, prostaglandin F 2-like compounds formed by free radical-catalyzed lipid peroxidation, are considered the most reliable markers of oxidative stress. It has been repeatedly suggested that newborns are exposed to conditions of oxidative stress resulting from the change from a low oxygen pressure in utero to a high oxygen pressure at birth. We measured the levels of F 2-isoprostanes in plasma of newborns by gas chromatography/mass spectrometry and we found that F 2-isoprostanes are significantly higher in term newborns compared to healthy adults. The greatest values were found in preterm newborns in whom F 2- isoprostanes are even higher than in term babies. Moreover a significant inverse correlation was found between the plasma levels of isoprostanes and the gestational age. A quite normal level of isoprostanes was found in the mothers both at delivery and during pregnancy. Placental total F 2- isoprostanes (sum of free plus esterified) were significantly higher in preterm compared to term deliveries and such a difference might account for the difference in plasma isoprostanes. Plasma non-protein-bound iron is higher in preterm than in term newborns, even if no correlation was found with plasma F 2-isoprostanes. Erythrocyte desferrioxamine-chelatable iron content (0 time) and release (24 h of aerobic incubation) are higher in newborns than in adults and in preterm than in term newborns, but again no correlation was found with plasma F 2-isoprostanes. The marked increase in plasma isoprostanes suggests that oxidative stress is a feature of the physiopathological changes seen in the perinatal period. © 2004 Elsevier Inc. All rights reserved.
2004
Comporti, M., Signorini, C., Leoncini, S., Buonocore, G., Rossi, V., Ciccoli, L. (2004). Plasma F2-isoprostanes are elevated in newborns and inversely correlated to gestational age. FREE RADICAL BIOLOGY & MEDICINE, 37(5), 724-732 [10.1016/j.freeradbiomed.2004.06.007].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/19127
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