Placental Amino Acids Transport in Intrauterine Growth Restriction

Avagliano, Laura; Garò, Chiara; Marconi, Anna Maria

doi:https://doi.org/10.1155/2012/972562

Journal of Pregnancy

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Volume 2012 | Article ID 972562 | https://doi.org/10.1155/2012/972562

Placental Amino Acids Transport in Intrauterine Growth Restriction

Laura Avagliano,¹Chiara Garò,¹and Anna Maria Marconi¹

Academic Editor: Timothy Regnault

Received15 Mar 2012

Accepted19 Apr 2012

Published11 Jul 2012

Abstract

The placenta represents a key organ for fetal growth as it acts as an interface between mother and fetus, regulating the fetal-maternal exchange of nutrients, gases, and waste products. During pregnancy, amino acids represent one of the major nutrients for fetal life, and both maternal and fetal concentrations are significantly different in pregnancies with intrauterine growth restriction when compared to uncomplicated pregnancies. The transport of amino acids across the placenta is a complex process that includes the influx of neutral, anionic, and cationic amino acids across the microvilluos plasma membrane of the syncytiotrophoblast, the passage through the cytoplasm of the trophoblasts, and the transfer outside the trophoblasts across the basal membrane into the fetal circulation. In this paper, we review the transport mechanisms of amino acids across the placenta in normal pregnancies and in pregnancies complicated by intrauterine growth restriction.

1. Introduction

The placenta represents a key organ for fetal growth as it acts as an interface between mother and fetus regulating the fetal-maternal exchange of nutrients, gases, water, ions, and waste products; moreover, it is capable of metabolic, immunologic, and endocrine functions.

In humans, the hemochorial placenta includes the syncytiotrophoblast (a continuous, uninterrupted, multinucleated surface that covers the villous tree), the cytotrophoblast (a second layer of mononucleated trophoblasts that become discontinuous as pregnancy progresses), the connective tissue of the villous tree, and the endothelium of the fetal capillaries. During pregnancy, the placenta grows in volume, weight, and in terms of development and maturation of the type of villi, to allow the optimal fetal-maternal exchange [1]. Terminal villi are the final ramifications of the villous tree, characterized by a very thin syncytiotrophoblastic layer facing the fetal capillaries with the least maternal-fetal distance. The syncytiotrophoblast, therefore, is the key structure in regulating transplacental exchange across its maternal and fetal facing: the microvillous plasma membrane (MVM) and the basal membrane, respectively (BM).

During pregnancy, amino acids represent one of the major nutrients for fetal life; they are important precursors for fetal development and growth, for the biosynthesis of proteins, nucleotides (purine and pyrimidine), neurotransmitters, and so forth. The transport of amino acids across the placenta is a complex process mediated by transporters located on the MVM and BM of the syncytiotrophoblast.

The purpose of this paper is to review the transport mechanisms of amino acids across the placenta in normal pregnancies and in pregnancies complicated by intrauterine growth restriction (IUGR).

2. Maternal and Fetal Concentrations

The fetal plasma concentration of most amino acids does not change during pregnancy and is significantly higher than maternal concentration [2–5], indicating an active transport across the placenta, from the maternal to the fetal circulation. In addition, in normal pregnancies, between maternal and fetal concentrations, there is a significant linear relationship for most amino acids leading to an increase in the umbilical venous concentration as maternal concentration increases [5, 6].

3. Placental Amino Acid Transport and Metabolism

The concentration of free amino acids in the placental tissue is higher than the concentration both in fetal and maternal plasma [2]; the placenta not only transports amino acids to the fetus, but its production and/or utilization of an amino acid plays an active role in determining its flux into the fetal circulation. In vivo animal studies have shown that the placenta is an extremely active organ metabolically with a very high rate of protein turnover and with some amino acids produced/utilized at very high rate. In addition, the presence of interorgan cycles of some nonessential amino acids between the placenta and fetal liver has been demonstrated: fetal glutamine and glycine are metabolized in the fetal liver and released to the placenta as glutamate and serine, respectively [7–11]. Studies performed in pregnant women with stable isotopes suggest that a similar interaction is present also in human pregnancies [12].

Many types of amino acid transport systems have been identified in the placenta [13] (Table 1). Each transporter is highly stereospecific, but different transporters have overlapping substrate specificity, with the possible compensation of one transporter activity by another [14].

Two major classes of amino acids transporters have been described: Na⁺-dependent transport systems (that mediate amino acids influx and lead to increased concentration of amino acids within the cell) and Na⁺-independent systems [19–21] (Table 1, Figure 1).

Figure 1

Mechanisms of amino acid transport. Na⁺-dependent transporters (T) permit the uptake of amino acids (aa) into the cell; amino acids are actively transported against a concentration gradient, using a Na⁺ gradient maintained by the Na⁺/K⁺ ATPasi. Amino acid exchangers (Ex) mediate the passage of amino acids by switching the position of one amino acid (aa1) from outside the cell and with one other (aa2) inside the cell. The transport across the basal membrane is poorly understood: may be mediate by amino acid exchangers (swapping one amino acid within the syncytiotrophoblast for one in the fetal capillary) or a nonexchanger passage may exist ( 972562.fig.002

) such as facilitate diffusion. (electron microscopy image: courtesy of GP Bulfamante; Diagram of amino acids transport modified from [15]).

As mentioned earlier, the syncytiotrophoblast is the key structure in regulating transplacental amino acids passage. The transport through the syncytiotrophoblast includes the influx of neutral, anionic, and cationic amino acids across the MVM, the passage through the cytoplasm of the trophoblasts, and the transfer outside the trophoblasts across the basal membrane into the fetal circulation. Placental amino acids transporters are present both at the microvillous and basal membrane levels. Whereas the transport across the MVM has been well studied, that across the BM is less understood: the transport into the MVM of the syncytiotrophoblast almost always requires energy to act against the concentration gradient (Na⁺-dependent transport systems); on the contrary, in the outflux of amino acid across the BM, Na⁺-independent systems have an important role [21]. The transport across the BM may be mediated by amino acid exchangers (that take one amino acid molecule from outside the cell and one from inside the cell and switch their position); moreover, recently, the presence and efficacy of some efflux transporters (TAT1, LAT3, LAT4) in the human BM have been reported in isolated perfused human placental cotyledons [22] suggesting that facilitate diffusion is possible across the syncytiotrophoblast basal membrane.

Furthermore, during pregnancy, an adaptive response to different fetal nutrient demands seems possible [23], based on the evidence of changes in placental transporters expression and activity during the course of gestation: it has been shown that the activity of system A increases [24]. In addition, it has been shown that, during pregnancy, the same amino acid may be transported through different systems, contingent to which membrane is being crossed: in term placentas, L-arginine transport across the microvillous membrane preparations seems to occur through both the y⁺ and y⁺L systems, while, in the basal membrane, transport may be restricted to the y⁺L system [25]. Altogether, these observations point to the complex interactions between the developing microvillous and basal membrane within the trophoblast and between the maternal and fetal circulations, to facilitate an increase in nutrient delivery to warrant the demand of the growing fetus [26]. In other words, the placenta acts as a “nutrient sensor” regulating its transporter function [18].

4. Intrauterine Growth Restriction

Intrauterine fetal growth is determined by a balance between fetal genetically determined growth potential and maternal-placental nutrients supply [27]. Some factors influence fetal nutrition: maternal nutrition and metabolism, utero-placental blood flow, placental size, and placental transfer capacity [28]. In pregnancies complicated by intrauterine growth restriction (IUGR), all these factors can be affected [29].

4.1. Maternal and Fetal Concentrations

The concentration of most amino acids is significantly decreased both in the umbilical artery and vein of IUGR pregnancies when compared to normally grown babies [5, 6, 30, 31]: in particular, small for gestational age fetuses have significantly lower concentrations of the essential branched chain amino acids valine, leucine, and isoleucine [5]. Furthermore, in IUGR, the maternal concentration of most essential amino acids is significantly higher than in pregnancies with appropriate for gestational age (AGA) fetuses, likely as a result of a maladaptation to pregnancy with a deficient hormone production: this observation, together with the presence of lower fetal amino acid concentrations in intrauterine growth restriction, leads to significantly lower fetal-maternal differences in these pregnancies [6, 30].

Moreover, in IUGR pregnancies, increasing the maternal concentration of amino acids leads to an increased umbilical uptake of some of the amino acids to the fetus but with no evidence of a change in the uptake of the essential amino acids valine, phenylalanine, lysine, histidine, and threonine suggesting the presence of competition for the same transporter across the placenta that might block transport [32].

Recently, we have also shown that the maternal concentration of most amino acids is significantly increased within 48 hours after the administration of antenatal corticosteroids, and this determines that the concentrations of phenylalanine, methionine, threonine, valine, leucine, serine, glycine, alanine, glutamine, and proline are also significantly increased both in the umbilical vein and artery when compared to controls. However, the umbilical venoarterial difference of total amino nitrogen was not significantly different from zero: overall, the results of this study suggest that, in IUGR pregnancies, corticosteroids not only increase maternal protein catabolism but increase fetal protein catabolism as well. In addition, despite an increase in protein catabolism, those amino acids with relatively large bidirectional flux across the placenta, such as leucine and phenylalanine, do not exhibit large increases in fetal concentration; on the contrary, other amino acids, with very little bidirectional flux, such as alanine and threonine, are trapped within the fetal circulation leading to the large increase in their concentrations [33]. Whether corticosteroids have a direct effect on the human placental amino acid transport systems, as it has been shown in the mouse placenta [34], needs to be determined.

4.2. Placental Amino Acid Transport and Metabolism

Studies we have performed in human pregnancies at the time of fetal blood sampling, during a constant infusion of L-[1-13]-leucine, have also shown that the fetomaternal leucine enrichment ratio progressively decreases in IUGR based on clinical severity [35]: this suggests not only that the transplacental flux of leucine is impaired but also a possible increased protein catabolism in these pregnancies [35]. In addition, if injected as a bolus into the maternal circulation of IUGR pregnancies, the fetomaternal enrichment ratio of two essential amino acids, leucine and phenylalanine, is significantly lower than in AGA pregnancies, again suggesting an impaired placental flux, whereas no differences are present for the nonessential amino acids, glycine, and proline [36].

However, as recently reviewed [21], some external factors may regulate the activity of amino acid transporters such as oxygen level [37], reactive oxygen species [38], insulin [37], leptin [39], and angiotensin II [40]. Therefore, it remains to be established whether the impairment of the amino acid transport system is the cause or the consequence of IUGR: we have shown that placental MVM system A activity not only is lower in IUGR compared with normal pregnancies but is also related to the severity of IUGR [41].

In vivo studies of placental amino acid transport and metabolism in the ovine heat-stress model of IUGR have shown a reduced flux of maternal leucine into the placenta and fetus [42]: this reduction is due to the reduction in placental and fetal mass and is accompanied by a decreased uteroplacental utilization of leucine. In addition, since uteroplacental oxygen and glucose consumption rates per gram of tissue remain within normal limits, the decrease in leucine utilization is not due to the general decline in metabolic rate [42]. In the same model, decreased fetoplacental threonine flux into the fetus and decreased fetoplacental threonine oxidation rate have been demonstrated indicating a downregulation of placental amino acids transport [43].

In severe IUGR fetal lambs (placental and fetal weights reduced by 40–60%), it has been shown that umbilical oxygen, glucose, and essential amino acid uptakes are significantly reduced compared to control animals whereas there are no differences in moderate IUGR (placental and fetal weights reduced by 25%) [44]. Two possible explanations have been proposed for these difference: first, since the placental diffusional exchange capacity of the severe IUGR fetus is significantly reduced, compared to AGA and moderate IUGR, changes in placental permeability and surface area might act as an impediment to control value uptakes per unit fetal weight; second, an upregulation of specific placental transport systems might be present since the mRNA expression of system L light chain components, LAT-1 and LAT-2, in severe IUGR is not different from control placentas, whereas it is significantly elevated in moderate IUGR [44].

In vitro studies of the human transport of amino acids have been performed [26]: in vesicle obtained from IUGR placentas, a reduced uptake of leucine and lysine has been reported, indicating a reduction of number or activity of the neutral and cationic amino acids transporters [45]; a decreased transport of taurine in isolated MVM has also been observed [46], suggesting a reduced activity of amino acid transporters. Furthermore, in MVM and BM vesicles from IUGR placentas, a decreased activity of system A (a sodium-dependent neutral amino acid transporter) has been shown [47–49], and the decreased activity of system A in MVM has been also related to the severity of IUGR [41]. Table 2 summarizes the alteration of amino acid transporters in the human placenta in IUGR pregnancies.

5. Fetal Programming

Evidence suggests that intrauterine fetal life is the mirror of what happens to human health in adult life [50]: abnormal intrauterine fetal growth (in excess or defect) is associated with the development of metabolic syndrome in adult life [50].

Epigenetic dysregulation may be the link between intrauterine events and adult disease; data from animal models suggest that nutrition in pregnancy could result in epigenetic modification [51]: a low-protein diet during pregnancy activates the placental amino acid response pathway in rats and programs the growth capacity of offspring [52]; moreover, in mice, maternal undernutrition alters the placental phenotype by adapting the expression of glucose and amino acids transporters to support fetal growth [53].

The metabolism of the fetus is adaptive and programmed to respond as expected to postnatal life [54]. Furthermore, as mentioned earlier, the placenta is a nutrient sensor [18]: if it senses an environment with low nutrient levels (deficit of maternal supply, such as in maternal undernutrition, alteration in substrate and oxygen level in maternal blood, alteration of placental blood flow), it increases its transport activity to allow normal fetal growth, by increasing the passage of nutrients from the maternal to fetal circulation; on the other hand, if there is an insufficient nutrient supply at the maternal side, the placenta may decrease its transport capacity, adapting fetal growth to a lower level, in order to reduce fetal (and postnatal) demand [55]. In addition, the placenta may modulate its transport activity even when it perceives an environment with a high nutritional content, as in gestational diabetic pregnancies. In these cases, an upregulation of glucose and amino acids transporters has been observed [55].

If the intrauterine environment may influence the epigenetic regulation, it is theoretically conceivable that impaired placental transport function could affect epigenetic regulation. In other word, the placenta may adapt fetal metabolism, and, therefore, the transport function of the placenta could be considered a “programming agent.”

References

C. J. P. Jones and H. Fox, “Ultrastructure of the normal human placenta,” Electron Microscopy Reviews, vol. 4, no. 1, pp. 129–178, 1991.
View at: Google Scholar
A. F. Philipps, I. R. Holzman, C. Teng, and F. C. Battaglia, “Tissue concentrations of free amino acids in term human placentas,” American Journal of Obstetrics and Gynecology, vol. 131, no. 8, pp. 881–887, 1978.
View at: Google Scholar
D. Montgomery and M. Young, “The uptake of naturally occurring amino acids by the plasma membrane of the human placenta,” Placenta, vol. 3, no. 1, pp. 13–19, 1982.
View at: Google Scholar
G. Soltesz, D. Harris, I. Z. Mackenzie, and A. Aynsley-Green, “The metabolic and endocrine milieu of the human fetus and mother at 18–21 weeks of gestation—I. Plasma amino acid concentrations,” Pediatric Research, vol. 19, no. 1, pp. 91–93, 1985.
View at: Google Scholar
I. Cetin, A. M. Marconi, P. Bozzetti et al., “Umbilical amino acid concentrations in appropriate and small for gestational age infants: a biochemical difference present in utero,” American Journal of Obstetrics and Gynecology, vol. 158, no. 1, pp. 120–126, 1988.
View at: Google Scholar
I. Cetin, S. Ronzoni, A. M. Marconi et al., “Maternal concentrations and fetal-maternal concentration differences of plasma amino acids in normal and intrauterine growth-restricted pregnancies,” American Journal of Obstetrics and Gynecology, vol. 174, no. 5, pp. 1575–1583, 1996.
View at: Publisher Site | Google Scholar
A. M. Marconi, F. C. Battaglia, G. Meschia, and J. W. Sparks, “A comparison of amino acid arteriovenous differences across the liver and placenta of the fetal lamb,” American Journal of Physiology: Endocrinology and Metabolism, vol. 257, no. 6, pp. E909–E915, 1989.
View at: Google Scholar
I. Cetin, P. V. Fennessey, A. N. Quick et al., “Glycine turnover and oxidation and hepatic serine synthesis from glycine in fetal lambs,” American Journal of Physiology: Endocrinology and Metabolism, vol. 260, no. 3, pp. E371–E378, 1991.
View at: Google Scholar
P. R. Vaughn, C. Lobo, F. C. Battaglia, P. V. Fennessey, R. B. Wilkening, and G. Meschia, “Glutamine-glutamate exchange between placenta and fetal liver,” American Journal of Physiology: Endocrinology and Metabolism, vol. 268, no. 4, pp. E705–E711, 1995.
View at: Google Scholar
F. C. Battaglia, “Glutamine and glutamate exchange between the fetal liver and the placenta,” Journal of Nutrition, vol. 130, no. 4, pp. 974S–977S, 2000.
View at: Google Scholar
C. L. Paolini, G. Meschia, P. V. Fennessey et al., “An in vivo study of ovine placental transport of essential amino acids,” American Journal of Physiology: Endocrinology and Metabolism, vol. 280, no. 1, pp. E31–E39, 2001.
View at: Google Scholar
I. Cetin, A. M. Marconi, A. M. Baggiani et al., “In vivo placental transport of glycine and leucine in human pregnancies,” Pediatric Research, vol. 37, no. 5, pp. 571–575, 1995.
View at: Google Scholar
F. C. Battaglia and T. R. H. Regnault, “Placental transport and metabolism of amino acids,” Placenta, vol. 22, no. 2-3, pp. 145–161, 2001.
View at: Publisher Site | Google Scholar
F. C. Battaglia, “Placental transport and utilization of amino acids and carbohydrates,” Federation Proceedings, vol. 45, no. 10, pp. 2508–2512, 1986.
View at: Google Scholar
J. K. Cleal and R. M. Lewis, “The mechanisms and regulation of placental amino acid transport to the human foetus,” Journal of Neuroendocrinology, vol. 20, no. 4, pp. 419–426, 2008.
View at: Publisher Site | Google Scholar
M. A. Grillo, A. Lanza, and S. Colombatto, “Transport of amino acids through the placenta and their role,” Amino Acids, vol. 34, no. 4, pp. 517–523, 2008.
View at: Publisher Site | Google Scholar
T. Jansson, “Amino acid transporters in the human placenta,” Pediatric Research, vol. 49, no. 2, pp. 141–147, 2001.
View at: Google Scholar
T. Jansson and T. L. Powell, “Human placental transport in altered fetal growth: does the placenta function as a nutrient sensor? A review,” Placenta, vol. 27, pp. 91–97, 2006.
View at: Publisher Site | Google Scholar
M. A. Grillo, A. Lanza, and S. Colombatto, “Transport of amino acids through the placenta and their role,” Amino Acids, vol. 34, no. 4, pp. 517–523, 2008.
View at: Publisher Site | Google Scholar
T. Jansson, “Amino acid transporters in the human placenta,” Pediatric Research, vol. 49, no. 2, pp. 141–147, 2001.
View at: Google Scholar
M. Desforges and C. P. Sibley, “Placental nutrient supply and fetal growth,” International Journal of Developmental Biology, vol. 54, no. 2-3, pp. 377–390, 2010.
View at: Publisher Site | Google Scholar
J. K. Cleal, J. D. Glazier, G. Ntani et al., “Facilitated transporters mediate net efflux of amino acids to the fetus across the basal membrane of the placental syncytiotrophoblast,” Journal of Physiology, vol. 589, no. 4, pp. 987–997, 2011.
View at: Publisher Site | Google Scholar
C. P. Sibley, P. Brownbill, M. Dilworth, and J. D. Glazier, “Adaptation in placental nutrient supply to meet fetal growth demand: implications for programming,” Placenta, vol. 31, pp. S70–S74, 2010.
View at: Publisher Site | Google Scholar
D. Mahendran, S. Byrne, P. Donnai et al., “Na+ transport, H+ concentration gradient dissipation, and system A amino acid transporter activity in purified microvillous plasma membrane isolated from first-trimester human placenta: comparison with the term microvillous membrane,” American Journal of Obstetrics and Gynecology, vol. 171, no. 6, pp. 1534–1540, 1994.
View at: Google Scholar
P. T. Y. Ayuk, C. P. Sibley, P. Donnai, S. D'Souza, and J. D. Glazier, “Development and polarization of cationic amino acid transporters and regulators in the human placenta,” American Journal of Physiology, vol. 278, no. 6, pp. C1162–C1171, 2000.
View at: Google Scholar
T. R. H. Regnault, J. E. Friedmann, R. B. Wilkening, R. V. Anthony, and W. W. Hay, “Fetoplacental transport and utilization of amino acids in IUGR—a review,” Placenta, vol. 26, pp. S52–S62, 2005.
View at: Publisher Site | Google Scholar
F. C. Battaglia and G. Meschia, An Introduction to Fetal Physiology, Academic Press, Orlando, Fla, USA, 1986.
T. Jansson, K. Ylvén, M. Wennergren, and T. L. Powell, “Glucose transport and system A activity in syncytiotrophoblast microvillous and basal plasma membranes in intrauterine growth restriction,” Placenta, vol. 23, no. 5, pp. 392–399, 2002.
View at: Publisher Site | Google Scholar
A. M. Marconi and C. L. Paolini, “Nutrient transport across the intrauterine growth-restricted placenta,” Seminars in Perinatology, vol. 32, no. 3, pp. 178–181, 2008.
View at: Publisher Site | Google Scholar
D. L. Economides, K. H. Nicolaides, W. A. Gahl, I. Bernardini, and M. I. Evans, “Plasma amino acids in appropriate- and small-for-gestational-age fetuses,” American Journal of Obstetrics and Gynecology, vol. 161, no. 5, pp. 1219–1227, 1989.
View at: Google Scholar
I. Cetin, C. Corbetta, L. Sereni et al., “Umbilical amino acid concentrations in normal and growth-retarded fetuses sampled in utero by cordocentesis,” American Journal of Obstetrics and Gynecology, vol. 162, no. 1, pp. 253–261, 1990.
View at: Google Scholar
S. Ronzoni, A. M. Marconi, C. L. Paolini, C. Teng, G. Pardi, and F. C. Battaglia, “The effect of a maternal infusion of amino acids on umbilical uptake in pregnancies complicated by intrauterine growth restriction,” American Journal of Obstetrics and Gynecology, vol. 187, no. 3, pp. 741–746, 2002.
View at: Publisher Site | Google Scholar
A. M. Marconi, V. Mariotti, C. Teng et al., “Effect of antenatal betamethasone on maternal and fetal amino acid concentration,” American Journal of Obstetrics and Gynecology, vol. 202, no. 2, pp. 166.e1–166.e6, 2010.
View at: Publisher Site | Google Scholar
O. R. Vaughan, P. M. Coan, and A. L. Fowden, “Maternal dexamethasone treatment retards growth but increases transport capacity of the mouse placenta at day 16 of pregnancy,” Reproductive Sciences, vol. 16, article 347A, 2009.
View at: Google Scholar
A. M. Marconi, C. L. Paolini, L. Stramare et al., “Steady state maternal-fetal leucine enrichments in normal and intrauterine growth-restricted pregnancies,” Pediatric Research, vol. 46, no. 1, pp. 114–119, 1999.
View at: Google Scholar
C. L. Paolini, A. M. Marconi, S. Ronzoni et al., “Placental transport of leucine, phenylalanine, glycine, and proline in intrauterine growth-restricted pregnancies,” Journal of Clinical Endocrinology and Metabolism, vol. 86, no. 11, pp. 5427–5432, 2001.
View at: Publisher Site | Google Scholar
D. M. Nelson, S. D. Smith, T. C. Furesz et al., “Hypoxia reduces expression and function of system A amino acid transporters in cultured term human trophoblasts,” American Journal of Physiology - Cell Physiology, vol. 284, no. 2, pp. C310–C315, 2003.
View at: Google Scholar
S. Khullar, S. L. Greenwood, N. McCord, J. D. Glazier, and P. T. Y. Ayuk, “Nitric oxide and superoxide impair human placental amino acid uptake and increase Na+ permeability: implications for fetal growth,” Free Radical Biology and Medicine, vol. 36, no. 3, pp. 271–277, 2004.
View at: Publisher Site | Google Scholar
N. Jansson, S. L. Greenwood, B. R. Johansson, T. L. Powell, and T. Jansson, “Leptin stimulates the activity of the system A amino acid transporter in human placental villous fragments,” Journal of Clinical Endocrinology and Metabolism, vol. 88, no. 3, pp. 1205–1211, 2003.
View at: Publisher Site | Google Scholar
E. Shibata, R. W. Powers, A. Rajakumar et al., “Angiotensin II decreases system A amino acid transporter activity in human placental villous fragments through AT1 receptor activation,” American Journal of Physiology: Endocrinology and Metabolism, vol. 291, no. 5, pp. E1009–E1016, 2006.
View at: Publisher Site | Google Scholar
J. D. Glazier, I. Cetin, G. Perugino et al., “Association between the activity of the system A amino acid transporter in the microvillous plasma membrane of the human placenta and severity of fetal compromise in intrauterine growth restriction,” Pediatric Research, vol. 42, no. 4, pp. 514–519, 1997.
View at: Google Scholar
J. C. Ross, P. V. Fennessey, R. B. Wilkening, F. C. Battaglia, and G. Meschia, “Placental transport and fetal utilization of leucine in a model of fetal growth retardation,” American Journal of Physiology: Endocrinology and Metabolism, vol. 270, no. 3, pp. E491–E503, 1996.
View at: Google Scholar
A. H. Anderson, P. V. Fennessey, G. Meschia, R. B. Wilkening, and F. C. Battaglia, “Placental transport of threonine and its utilization in the normal and growth-restricted fetus,” American Journal of Physiology: Endocrinology and Metabolism, vol. 272, no. 5, pp. E892–E900, 1997.
View at: Google Scholar
T. R. H. Regnault, A. M. Marconi, C. H. Smith et al., “Placental amino acid transport systems and fetal growth restriction—a workshop report,” Placenta, vol. 26, pp. S76–S80, 2005.
View at: Publisher Site | Google Scholar
T. Jansson, V. Scholtbach, and T. L. Powell, “Placental transport of leucine and lysine is reduced in intrauterine growth restriction,” Pediatric Research, vol. 44, no. 4, pp. 532–537, 1998.
View at: Google Scholar
S. Norberg, T. L. Powell, and T. Jansson, “Intrauterine growth restriction is associated with a reduced activity of placental taurine transporters,” Pediatric Research, vol. 44, no. 2, pp. 233–238, 1998.
View at: Google Scholar
D. Mahendran, P. Donnai, J. D. Glazier, S. W. D'Souza, R. D. H. Boyd, and C. P. Sibley, “Amino acid (system A) transporter activity in microvillous membrane vesicles from the placentas of appropriate and small for gestational age babies,” Pediatric Research, vol. 34, no. 5, pp. 661–665, 1993.
View at: Google Scholar
J. M. Dicke and D. K. Verges, “Neutral amino acid uptake by microvillous and basal plasma membrane vesicles from appropriate- and small-for-gestational age human pregnancies,” Journal of Maternal-Fetal Medicine, vol. 3, no. 6, pp. 246–250, 1994.
View at: Google Scholar
T. Jansson, K. Ylvén, M. Wennergren, and T. L. Powell, “Glucose transport and system A activity in syncytiotrophoblast microvillous and basal plasma membranes in intrauterine growth restriction,” Placenta, vol. 23, no. 5, pp. 392–399, 2002.
View at: Publisher Site | Google Scholar
D. J. P. Barker, “In utero programming of chronic disease,” Clinical Science, vol. 95, no. 2, pp. 115–128, 1998.
View at: Google Scholar
R. A. Waterland and K. B. Michels, “Epigenetic epidemiology of the developmental origins hypothesis,” Annual Review of Nutrition, vol. 27, pp. 363–388, 2007.
View at: Publisher Site | Google Scholar
R. S. Strakovsky, D. Zhou, and Y. X. Pan, “A low-protein diet during gestation in rats activates the placental mammalian amino acid response pathway and programs the growth capacity of offspring,” Journal of Nutrition, vol. 140, no. 12, pp. 2116–2120, 2010.
View at: Publisher Site | Google Scholar
P. M. Coan, O. R. Vaughan, Y. Sekita et al., “Adaptations in placental phenotype support fetal growth during undernutrition of pregnant mice,” Journal of Physiology, vol. 588, no. 3, pp. 527–538, 2010.
View at: Publisher Site | Google Scholar
N. W. Solomons, “Developmental origins of health and disease: concepts, caveats, and consequences for public health nutrition,” Nutrition Reviews, vol. 67, no. 1, supplement, pp. S12–S16, 2009.
View at: Publisher Site | Google Scholar
T. Jansson, K. Ylvén, M. Wennergren, and T. L. Powell, “Glucose transport and system A activity in syncytiotrophoblast microvillous and basal plasma membranes in intrauterine growth restriction,” Placenta, vol. 23, no. 5, pp. 392–399, 2002.
View at: Publisher Site | Google Scholar

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Copyright © 2012 Laura Avagliano et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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