Literature DB >> 12562948

Placental glucose transport in growth-restricted pregnancies induced by overnourishing adolescent sheep.

Jacqueline M Wallace1, Deirdre A Bourke, Raymond P Aitken, John S Milne, William W Hay.   

Abstract

Glucose clamp procedures were used to determine whether the slowing of fetal growth during the final third of gestation in overnourished adolescent ewes is due to a reduction in placental glucose transport capacity. Singleton pregnancies to a single sire were established by embryo transfer and thereafter adolescent dams were offered a high (n = 11) or moderate (n = 7) nutrient intake. Studies were conducted at 130 +/- 0.5 days gestation. Uterine and umbilical blood flows were studied by the steady-state transplacental diffusion technique and glucose fluxes quantified by the Fick principle. To determine the relationship between the transplacental glucose gradient and umbilical (fetal) glucose uptake, studies were conducted with maternal arterial glucose clamped at 5 micromol ml(-1) and fetal glucose at spontaneously occurring and two additional higher levels. Maternal body weight gain during gestation averaged 282 and 57 g day(-1) for high- and moderate-intake dams, respectively. Total placentome weight (209 +/- 23 vs. 386 +/- 34 g) and fetal weight (3072 +/- 266 vs. 4670 +/- 196 g) were lower (P < 0.001) in high- than in moderate-intake groups. The growth-restricted pregnancies in the high-intake dams were associated with reduced uterine (P < 0.05) and umbilical (P < 0.02) blood flows and, in the non-perturbed state, the fetuses were relatively hypoxic (2.1 vs. 3.0 micromol ml(-1), P < 0.05) and hypoglycaemic (0.90 vs. 1.31 micromol ml(-1), P < 0.002). Linear regression analysis of umbilical glucose uptake at three steady-state uterine-umbilical arterial transplacental plasma glucose concentration gradients revealed that absolute placental glucose transport capacity was lower in high- than in moderate-intake dams (mean slope, 0.8 vs. 1.5 dl min(-1), P < 0.05; and mean intercept, 1.84 vs. 3.40 micromol ml(-1)). However, glucose transfer capacity was not different between the two groups when expressed on a placental weight-specific basis. This confirms that the small size of the placenta per se is the major limitation to placental glucose transfer in the overnourished adolescent pregnant sheep.

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Year:  2002        PMID: 12562948      PMCID: PMC2342623          DOI: 10.1113/jphysiol.2002.023333

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  27 in total

1.  Switching maternal dietary intake at the end of the first trimester has profound effects on placental development and fetal growth in adolescent ewes carrying singleton fetuses.

Authors:  J M Wallace; D A Bourke; R P Aitken; M A Cruickshank
Journal:  Biol Reprod       Date:  1999-07       Impact factor: 4.285

2.  Uterine blood flow, oxygen and glucose uptakes at mid-gestation in the sheep.

Authors:  R D Molina; G Meschia; R B Wilkening
Journal:  Proc Soc Exp Biol Med       Date:  1990-12

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Authors:  W W Hay; H K Meznarich
Journal:  Q J Exp Physiol       Date:  1986-10

4.  Nutrient partitioning and fetal growth in rapidly growing adolescent ewes.

Authors:  J M Wallace; R P Aitken; M A Cheyne
Journal:  J Reprod Fertil       Date:  1996-07

5.  Effect of restriction of placental growth on fetal and utero-placental metabolism.

Authors:  J A Owens; J Falconer; J S Robinson
Journal:  J Dev Physiol       Date:  1987-06

6.  Effect of restriction of placental growth on umbilical and uterine blood flows.

Authors:  J A Owens; J Falconer; J S Robinson
Journal:  Am J Physiol       Date:  1986-03

7.  Effect of high levels of insulin on glucose utilization and glucose production in pregnant and nonpregnant sheep.

Authors:  W W Hay; C C Lin; H K Meznarich
Journal:  Proc Soc Exp Biol Med       Date:  1988-12

Review 8.  Nutrient partitioning during adolescent pregnancy.

Authors:  J Wallace; D Bourke; P Da Silva; R Aitken
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9.  Glucose metabolism in pregnant sheep when placental growth is restricted.

Authors:  J A Owens; J Falconer; J S Robinson
Journal:  Am J Physiol       Date:  1989-08

10.  Fetal CO2 kinetics.

Authors:  L C Van Veen; W W Hay; F C Battaglia; G Meschia
Journal:  J Dev Physiol       Date:  1984-08
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  22 in total

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Review 5.  The intrauterine growth restriction phenotype: fetal adaptations and potential implications for later life insulin resistance and diabetes.

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8.  Effect of timing of iron supplementation on maternal and neonatal growth and iron status of iron-deficient pregnant rats.

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9.  Placental transport in response to altered maternal nutrition.

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Review 10.  Placental-fetal glucose exchange and fetal glucose metabolism.

Authors:  William W Hay
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