Fructose in fetal cord blood and its relationship with maternal and 48-hour-newborn blood concentrations

被引:20
作者
Trindade, Cleide E. P. [1 ]
Barreiros, Rodrigo C. [2 ]
Kurokawa, Cilmery [1 ]
Bossolan, Grasiela [1 ]
机构
[1] Sao Paulo State Univ, UNESP, Botucatu Sch Med, Dept Pediat,Div Neonatol, BR-18618970 Sao Paulo, Brazil
[2] PUCSP Sorocaba, Sch Med, Dept Med Pediat, BR-18030095 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Newborn fructose metabolism; Fetus fructose metabolism; Fructose; SUGAR ALCOHOL CONCENTRATIONS; INSULIN-RESISTANCE; SORBITOL PATHWAY; HUMAN-PLASMA; HUMAN-MILK; GLUCOSE; METABOLISM; OXIDATION; CHROMATOGRAPHY; CARBOHYDRATE;
D O I
10.1016/j.earlhumdev.2010.12.005
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Studies have suggested that different non-glucose sugars and sugar alcohols play a role in placental and fetal metabolism. However, the role of fructose in the fetal and newborn metabolism is unclear and studies are scarce. Aim: Our objective was to investigate the presence of fructose in umbilical cord blood in full-term gestation and its relationship with maternal and 48-hour-old- newborn blood concentrations, to evaluate fructose production by the fetus and newborn infant. Methods: Blood fructose and glucose concentrations were determined by HPLC in 26 paired samples of maternal blood, umbilical cord vein, and peripheral newborn blood at 48 h after birth. ANOVA, the Friedman Analysis of variance on Ranks and the Pearson correlation with p<0.05 were used. Results: Fructose concentration in umbilical cord blood was higher than maternal blood (p = 0.024), suggesting endogenous fructose production by the fetal-placental unit via the sorbitol pathway. Fructose concentrations were higher in newborns at 48 h after birth than in the fetal umbilical cord blood (p = 0.004), suggesting that fructose production is a continuous process from fetus to newborn. Conclusions: Fructose production by the sorbitol pathway, present in the fetus and newborn, is an alternative pathway in glucose metabolism probably used to maintain redox balance in the fetus. We suggest that endogenous fructose, similar to dietary ingested fructose, under physiological conditions produces the backbone for triacylglycerol and lipid synthesis in the fetus and newborn. Therefore the route for metabolizing fructose is already present in the early steps of human development. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:193 / 197
页数:5
相关论文
共 31 条
[1]   A United States national reference for fetal growth [J].
Alexander, GR ;
Himes, JH ;
Kaufman, RB ;
Mor, J ;
Kogan, M .
OBSTETRICS AND GYNECOLOGY, 1996, 87 (02) :163-168
[2]  
BERNIRSCHKE K, 2004, NEOREVIEWS, V5, pE252
[3]   Blood galactose and glucose levels in mothers, cord blood, and 48-hour-old breast-fed full-term infants [J].
Bossolan, Grasiela ;
Trindade, Cleide E. P. ;
Barreiros, Rodrigo Crespo .
NEONATOLOGY, 2007, 91 (02) :121-126
[4]  
BRACHET EA, 1973, BIOL NEONATE, V23, P314
[5]  
Bray GA, 2004, AM J CLIN NUTR, V79, P537
[6]   Fetal and maternal non-glucose carbohydrates and polyols concentrations in normal human pregnancies at term [J].
Brusati, V ;
Józwik, M ;
Józwik, M ;
Teng, C ;
Paolini, C ;
Marconi, AM ;
Battaglia, FC .
PEDIATRIC RESEARCH, 2005, 58 (04) :700-704
[7]   Free sugar and sugar alcohol concentrations in human breast milk [J].
Cavalli, C ;
Teng, C ;
Battaglia, FC ;
Bevilacqua, G .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2006, 42 (02) :215-221
[8]   Mechanisms for the acute effect of fructose on postprandial lipemia [J].
Chong, Mary F-F ;
Fielding, Barbara A. ;
Frayn, Keith N. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2007, 85 (06) :1511-1520
[9]  
COPPA GV, 1993, PEDIATRICS, V91, P637
[10]   Fructose, weight gain, and the insulin resistance syndrome [J].
Elliott, SS ;
Keim, NL ;
Stern, JS ;
Teff, K ;
Havel, PJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (05) :911-922