Glutathione recycling and antioxidant enzyme activities in erythrocytes of term and preterm newborns at birth

被引:50
作者
Frosali, S
Di Simplicio, P
Perrone, S
Di Giuseppe, D
Longini, M
Tanganelli, D
Buonocore, G
机构
[1] Univ Siena, Policlin Le Scotte, Dept Pediat Obstet & Reprod Med, IT-53100 Siena, Italy
[2] Univ Siena, Dept Neurosci, Pharmacol Unit, I-53100 Siena, Italy
来源
BIOLOGY OF THE NEONATE | 2004年 / 85卷 / 03期
关键词
newborn infant; erythrocytes; red blood cell redox potential; glutathione recycling; antioxidant defenses;
D O I
10.1159/000075814
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We previously demonstrated a high susceptibility of neonatal red blood cells (RBC) to oxidative stress at birth. The aim of this study was to compare the RBC antioxidant capacity and redox cycle enzyme activities as well as glutathione (GSH) recycling in full-term and preterm infants at birth and in normal adults. GSH and GSH disulfide (GSSG) concentrations, GSH/GSSG ratio, and the activities of glucose-6-phosphate dehydrogenase (G-6-PDH), GSH peroxidase, GSH reductase (GR), catalase (CAT), superoxide dismutase (SOD), and hexokinase (HK) were measured in RBC of 25 healthy adults and 56 newborns (23 term, 33 preterm) at birth. The GSH recycling was measured in adult and newborn RBC exposed to oxidative stress (1 mM tert-butylhydroperoxide). The RBC of term and preterm babies showed higher GSH, GSSG, G-6-PDH, GR, and HK levels/activities and lower GSH/GSSG ratios and higher GSH-recycling rates than those of adults. In preterm babies significant correlations were found between G-6-PDH and CAT, GSH, GSH/GSSG ratio, and GSSG (r = -0.67, r = 0.71, r = -0.66, p < 0.01; r = 0.71, p < 0.05, respectively). In term newborns, statistically significant correlations were observed between G-6-PDH and CAT, SOD, and GSH (r = -0.65, r = -0.65, r = -0.69, p < 0.01, respectively). The results indicate the central role of the G-6-PDH activity in antioxidant defenses. We speculate that preterm babies have prompter involvement of antioxidant defenses than term babies. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:188 / 194
页数:7
相关论文
共 36 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]  
BEUTLER E, 1979, RED CELL METABOLISM, P83
[3]  
BEUTLER E, 1979, RED CELL METABOLISM, P68
[4]  
BRACCI R, 1990, INT CONGR SER, V952, P55
[5]  
Bracci R., 1998, SEMIN NEONATOL, V3, P191, DOI [10.1016/S1084-2756(98)80004-3, DOI 10.1016/S1084-2756(98)80004-3]
[6]   Total hydroperoxide and advanced oxidation protein products in preterm hypoxic babies [J].
Buonocore, G ;
Perrone, S ;
Longini, M ;
Terzuoli, L ;
Bracci, R .
PEDIATRIC RESEARCH, 2000, 47 (02) :221-224
[7]   Oxidative stress in preterm neonates at birth and on the seventh day of life [J].
Buonocore, G ;
Perrone, S ;
Longini, M ;
Vezzosi, P ;
Marzocchi, B ;
Paffetti, P ;
Bracci, R .
PEDIATRIC RESEARCH, 2002, 52 (01) :46-49
[8]  
Buonocore G, 2001, BIOL NEONATE, V79, P180
[9]   Intraerythrocyte nonprotein-bound iron and plasma malondialdehyde in the hypoxic newborn [J].
Buonocore, G ;
Zani, S ;
Perrone, S ;
Caciotti, B ;
Bracci, R .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (07) :766-770
[10]  
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484