Ovine placental and fetal arginine metabolism at normal and increased maternal plasma arginine concentrations

被引:29
作者
Thureen, PJ [1 ]
Baron, KA [1 ]
Fennessey, PV [1 ]
Hay, WW [1 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Pediat, Perinatal Res Ctr,Sect Neonatol, Denver, CO 80262 USA
关键词
D O I
10.1203/00006450-200204000-00011
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Arginine (A) may play a significant role in fetal growth, by stimulating insulin secretion and as a precursor for both polyamine synthesis and nitric oxide production. To determine whether increased maternal plasma A concentrations can enhance delivery of A to the fetus, uterine, umbilical, and net uteroplacental (UP) A uptake rates were measured in 12 pregnant ewes at 129.6 +/- 0.4 d gestation (mean +/- SEM) during normal and after 3 h of increased maternal plasma A concentrations. With a 2.7-fold increase in maternal plasma A concentrations (p < 0.001), there were significant increases in uterine A uptake (13.8 +/- 1.0 to 41.3 +/- 7.7 mu mol/min, p < 0.005), umbilical A uptake (3.3 +/- 0.5 to 5.2 +/- 0.8 mumol-min(-1).kg(-1) fetus, p < 0.005), UP A uptake (17.8 +/- 6.2 to 89.2 +/- 20.3 mu mol.min (1).kg(-1) placenta, p < 0.01), fetal arterial A concentration (98.7 +/- 6.3 to 137.1 +/- 9.9 muM, p < 0.001), maternal A disposal rate (143.7 +/- 9.4 to 217.0 +/- 6.7 mu mol/min, p < 0.001), fetal A disposal rate (7.9 +/- 0.8 to 9.9 +/- 1.1 mumol.min(-1).kg(-1) p < 0.05), fetal A oxidation rate (1.31 +/- 0.24 to 1.84 +/- 0.36 mu mol.min(-1).kg(-1), p < 0.05), and plasma insulin concentration in both fetus (16 +/- 2 to 20 +/- 2 muU/mL, p < 0.001) and mother (24 +/- 3 to 32 +/- 4 mu U/mL, p < 0.001). Thus, increased maternal plasma A concentration increases maternal. UP. and fetal A net uptake, and increases insulin secretion in mother and fetus. The 4.2-fold larger increase in UP than net fetal A uptake could represent preferential UP A metabolism relative to fetal A metabolism, relatively limited placental-fetal A transport capacity compared with uterine A uptake capacity, or both; responsible mechanisms remain unknown.
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页码:464 / 471
页数:8
相关论文
共 32 条
[1]   Maturation of glucose-stimulated insulin secretion in fetal sheep [J].
Aldoretta, PW ;
Carver, TD ;
Hay, WW .
BIOLOGY OF THE NEONATE, 1998, 73 (06) :375-386
[2]   Development and polarization of cationic amino acid transporters and regulators in the human placenta [J].
Ayuk, PTY ;
Sibley, CP ;
Donnai, P ;
D'Souza, S ;
Glazier, JD .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 278 (06) :C1162-C1171
[3]   UREA CYCLE INTERMEDIATE KINETICS AND NITRATE EXCRETION AT NORMAL AND THERAPEUTIC INTAKES OF ARGININE IN HUMANS [J].
BEAUMIER, L ;
CASTILLO, L ;
AJAMI, AM ;
YOUNG, VR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (05) :E884-E896
[4]  
Beaumier Louis, 1996, Biomedical and Environmental Sciences, V9, P296
[5]   GLUCOSE SUPPRESSION OF INSULIN-SECRETION IN CHRONICALLY HYPERGLYCEMIC FETAL SHEEP [J].
CARVER, TD ;
ANDERSON, SM ;
ALDORETTA, PA ;
ESLER, AL ;
HAY, WW .
PEDIATRIC RESEARCH, 1995, 38 (05) :754-762
[6]   Production and utilization of amino acids by ovine placenta in vivo [J].
Chung, M ;
Teng, C ;
Timmerman, M ;
Meschia, G ;
Battaglia, FC .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1998, 274 (01) :E13-E22
[7]  
Eaton BM, 1998, EUR J CLIN INVEST, V28, P1006
[8]   ENZYME-ACTIVITIES IN SHEEP PLACENTA DURING LAST 3 MONTHS OF PREGNANCY [J].
EDWARDS, EM ;
RATTENBURY, JM ;
VARNAM, GCE ;
DHAND, UK ;
JEACOCK, MK ;
SHEPHERD, DAL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 497 (01) :133-143
[9]  
Fisker S., 1999, Journal of Endocrinological Investigation, V22, P89
[10]   THE ROLE OF INSULIN IN FETAL GROWTH [J].
FOWDEN, AL .
EARLY HUMAN DEVELOPMENT, 1992, 29 (1-3) :177-181