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Am J Physiol Endocrinol Metab 295: E170-E178, 2008. First published May 20, 2008; doi:10.1152/ajpendo.00047.2008
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Repeated betamethasone treatment of pregnant sheep programs persistent reductions in circulating IGF-I and IGF-binding proteins in progeny

Kathryn L. Gatford,1 Julie A. Owens,1 Shaofu Li,2 Timothy J. M. Moss,2,3 John P. Newnham,2,3 John R. G. Challis,4 and Deborah M. Sloboda2,3

1Research Centre for Early Origins of Adult Disease, Discipline of Obstetrics and Gynecology, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide; 2School of Women's and Infant's Health, The University of Western Australia, Perth; 3Women and Infants Research Foundation of Western Australia, Subiaco, Perth, Australia; and 4Canadian Institutes of Health Research Group in Fetal and Neonatal Health and Development, Departments of Physiology and Obstetrics and Gynecology, University of Toronto, Ontario, Canada

Submitted 24 January 2008 ; accepted in final form 15 May 2008


   ABSTRACT
TOP
 ABSTRACT
MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
Exposure to synthetic glucocorticoids in utero markedly improves survival after preterm birth, but repeated exposures impair fetal and postnatal growth and are associated with evidence of insulin resistance in later life. The insulin-like growth factor (IGF) axis is an important regulator of growth and metabolism before and after birth. We have therefore investigated the effects of repeated maternal betamethasone injections on plasma IGF-I, IGF-II, and IGF-binding proteins (IGFBP) in fetal and postnatal progeny in the sheep. Pregnant sheep carrying male fetuses were injected with saline or betamethasone at 104, 111, and 118 days of gestation (dG, term ~150 dG). Plasma samples were collected postmortem from fetuses before (75, 84, 101 dG) or after one (109 dG), two (116 dG), or three (121–122, 132–133, 145–147 dG) doses of saline or betamethasone and from progeny at 42 and 84 days of age. Fetal weight was reduced after two or more maternal betamethasone injections, and this effect persisted to term. Repeated betamethasone exposures reduced plasma IGF-I and total IGFBP in fetuses at 133 dG and progeny at 84 days, and reduced plasma IGFBP-3 at 84 days. Fetal plasma IGF-II tended to increase transiently at 109 dG following the first betamethasone injection. Fetal, placental, and/or postnatal weights correlated positively with concomitant plasma IGF-I, IGF-II, and total IGFBP. We conclude that repeated exposure to synthetic glucocorticoids in utero programs the IGF axis before and after birth, which may contribute to the adverse effects of betamethasone exposure on growth and metabolism.

antenatal glucocorticoids; pregnancy; programming; insulin-like growth factor-binding protein

INJECTION OF WOMEN in preterm labor with synthetic corticosteroids accelerates fetal lung maturation and consequently markedly reduces mortality and morbidity in their premature infants (47). Follow-up of infants born to mothers enrolled in the first randomized control trial (RCT) of a single betamethasone course given to women in preterm labor showed improved neonatal and childhood outcomes (47). Although blood pressure and health-related quality of life scores were similar in 31-yr-old adults whose mothers had betamethasone or saline before preterm delivery, those who were exposed to synthetic corticosteroids in utero had larger insulin responses to an oral glucose challenge, suggestive of insulin resistance (12, 47). In Australia, over 90% of obstetricians choose betamethasone as the synthetic corticosteroid for use in cases of threatened preterm labor, with smaller numbers using alternates, including dexamethasone (46). Although dexamethasone has cost advantages over betamethasone, recent data from the United States National Institute of Child Health and Human Development Neonatal Research Network support use of betamethasone in preference to dexamethasone, due to better long-term neurodevelopmental outcomes, as well as higher neonatal survival rates following preterm birth (31).

Clinically, use of repeated glucocorticoid administration to mothers at continued risk of preterm labor appears widespread, although it is not recommended (42, 46). An initial report from a large RCT concluded that repeated courses of synthetic corticosteroid were more effective than single doses in decreasing respiratory distress syndrome and severe lung disease in infants (11), and single doses did not reduce the risk of respiratory distress syndrome in infants born >7 days after exposure to corticosteroids (36). Nevertheless, repeated, but not single, exposure to synthetic corticosteroids reduced size at birth (9, 11) and increased neonatal blood pressure of infants (37).

In sheep, like humans, repeated maternal injections of betamethasone at doses similar to those used clinically in women impair fetal growth, whereas in most studies (6, 40, 41, 51), although not all (27), a single injection did not impair fetal growth. Sheep whose mothers were injected with four doses of betamethasone at 7-day intervals from 104 days gestational age [104 days gestation (dG), term ~150 dG] also had greater insulin responses to a glucose challenge as young adults and higher fasting plasma insulin-to-glucose ratio in adulthood than those whose mothers received saline (41, 50). This suggests insulin resistance also occurs in the sheep following repeated fetal exposure to synthetic corticosteroid.

A mechanistic link between in utero exposure to synthetic corticosteroids and these later adverse outcomes may be programming of the insulin-like growth factor (IGF) axis, which is important for growth and metabolism before and after birth. Gene deletion studies in mice have shown that IGF-I is the most critical IGF for fetal and postnatal growth, whereas IGF-II regulates placental and fetal, but not postnatal, growth (3, 15). Consistent with their roles in growth regulation, fetal and neonatal plasma IGF-I and IGF-II concentrations are usually reduced in human intrauterine growth restriction (IUGR) (30, 32, 33), as well as in experimental IUGR in rats and sheep (5, 43, 56). The IGF axis is also an important regulator of glucose homeostasis. IGF-I can directly stimulate glucose uptake, and low plasma IGF-I predicts poor insulin secretion in children and later development of impaired glucose tolerance in adults (17, 57).

Evidence from human and animal studies has shown that exposure to synthetic glucocorticoids in utero changes the circulating abundance of IGF and IGF-binding proteins (IGFBPs) in the fetus and that this persists at least up to birth. In humans, the impact of administration of synthetic corticosteroids on the IGF axis has been studied only in premature neonates at or shortly after delivery. Treatment with a single course of betamethasone did not change IGF-I or IGFBP-3 but decreased IGF-II and IGFBP-1 in umbilical cord serum or umbilical vein plasma of infants <37 wk gestational age, even when betamethasone exposure occurred >2 wk before delivery (1, 55). Repeated exposure to synthetic corticosteroids may have more profound effects on the neonatal IGF axis. Kajantie et al. (29) reported that exposure to increasing courses of betamethasone increased cord plasma IGF-I and IGFBP-3 concentrations and decreased those of IGF-II and IGFBP-1. In contrast to the effects reported in humans, maternal treatment with betamethasone or dexamethasone in rats on days 12 and 13 of pregnancy (term 21–22 days) reduced plasma IGF-I and increased plasma IGFBP-1 concentrations in the fetus at term (38). In the rat, longer courses of maternal dexamethasone treatment (days 13 to 20 or 15 to 19) also increased IGF-II, type 1 IGF-receptor, IGFBP-1, and IGFBP-2 gene expression and decreased IGFBP-3 gene expression in fetal tissues, without altering IGF-I expression, while reducing IGF-II expression in placenta (2, 45). The fetal IGF-I response to glucocorticoid exposure in rabbits resembles that in humans, with increased plasma IGF-I and tissue IGF-I expression, particularly in naturally growth-restricted fetuses (53). Whether any effects of prenatal exposure to synthetic glucocorticoids on the IGF axis extend beyond the perinatal period has not been reported for any species.

We have therefore investigated the effect of repeated betamethasone injections of the pregnant sheep on development of the IGF axis in fetal and postnatal progeny, and the relationships between fetal and postnatal growth and IGF abundance, to determine whether programming of the IGF axis is associated with impaired fetal and postnatal growth following repeated exposure to synthetic glucocorticoid in utero.


   MATERIALS AND METHODS
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 ABSTRACT
 MATERIALS AND METHODS
RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 
All experimental procedures were approved by the Animal Experimentation Ethics Committee of the Western Australian Department of Agriculture and were performed according to the National Health and Medical Research Council Australian Code of Practice for the Care and Use of Animals for Scientific Purposes, 7th edition, 2004. Betamethasone treatment, management of pregnant ewes, and collection of fetal samples were reported previously for this cohort (6).

Animals and prenatal treatments. Ewes bearing singleton male fetuses of known gestation were used in the study. Fetal sex was determined either by ultrasound at 50 dG or by DNA extraction of fetal cells from amniotic fluid samples collected by amniocentesis at 60 dG. Sex was determined using nested allele-specific PCR amplification of zfx and zfy gene fragments, as previously reported (16). All progeny in this study were intact males (i.e., not castrated).

All ewes received an intramuscular injection of 150 mg medroxyprogesterone acetate (Depo Provera; Upjohn) at 100 dG to reduce pregnancy losses due to subsequent glucocorticoid treatment (41, 52). Ewes were then randomly allocated to control or betamethasone groups. Animals in the betamethasone group received intramuscular injections of 0.5 mg/kg body wt betamethasone (Celestone Chronodose; Schering Plough) at 104, 111, and 118 dG. Animals in the control group received saline injections of a comparable volume (5–6 ml) at the same gestational ages. Betamethasone was chosen for its clinical relevance, since it is the main synthetic corticosteroid used in cases of threatened preterm labor within Australia (46).

Plasma samples were collected at postmortem before (75, 84, 101 dG), during (109, 116 dG), or after (121, 132, 146 dG and at 42 and 84 postnatal days of age) either saline or betamethasone injections. For fetal collections, pregnant ewes were killed with captive bolt, fetuses were delivered by Caesarean section, umbilical arterial blood was collected, and fetuses were weighed and then killed by decapitation. For collection from postnatal progeny, pregnant ewes that had received three injections of betamethasone or saline during pregnancy were permitted to deliver spontaneously, and lambs were kept with ewes until the time of death. At postmortem, blood samples were collected by jugular venipuncture; lambs were sedated with ketamine (15 mg/kg) and xylazine (0.1 mg/kg; Troy Laboratories, Smithfield, NSW, Australia) and then killed by decapitation.

Measurement of plasma IGF-I, IGF-II, and total IGFBP. Plasma IGF-I and -II were measured by RIA after separation of IGF and IGFBP by size-exclusion HPLC under acidic conditions (44). Maternal and fetal plasma samples were injected onto separate HPLC columns, dedicated to ovine postnatal or fetal samples, respectively. Four fractions of eluate (fraction 1, containing IGFBP; fraction 2, interpeak; fraction 3, containing IGF, and fraction 4, postpeak) were routinely collected for each acidified plasma specimen, using times determined for each column based on elution times of 125I-labeled IGF-I and IGF immunoreactivity. Recovery of 125I-IGF-I was 100.0 ± 0.9% for seven HPLC runs of fetal plasma and was 103.6% for a single HPLC run containing all postnatal samples for the study.

Plasma IGF-I concentrations were measured by analysis of neutralized HPLC fraction 3, in a RIA specific for IGF-I (20), using a rabbit polyclonal antibody to human IGF-I (GroPep Australia). Total IGFBP concentrations were measured by analysis of neutralized HPLC fraction 1 in the same assay. Because IGFBP bind to and sequester 125I-IGF-I in this assay, they can be measured due to their effect of reducing the amount of 125I-IGF-I in the immunoprecipated pellet, giving an apparent IGF concentration that reflects the total amount and binding affinity of IGFBP present in plasma. Samples were assayed in triplicate. Inter- and intra-assay covariances for an HPLC eluate fraction 3 pool prepared from ovine plasma containing 124.5 ng/ml IGF-I were 9.8 and 7.3% respectively (n = 5 assays). Covariance for extraction and assay of a fetal plasma quality control pool containing 235 ng/ml IGF-I, and included in each HPLC run of fetal samples, was 17.2% (n = 7 HPLC runs).

Plasma IGF-II concentrations were measured by analysis of HPLC fraction 3 in a RIA specific for IGF-II (8), using a rabbit polyclonal antibody against human IGF-II (GroPep). Samples were assayed in triplicate. Inter- and intra-assay coefficients of variation for an HPLC eluate fraction 3 pool prepared from ovine plasma containing 167 ng/ml IGF-II were 3.4 and 9.0%, respectively (n = 3 assays). Covariance for extraction and assay of a fetal plasma QC containing 396 ng/ml IGF-II, and included in each HPLC run of fetal samples, was 16.4% (n = 7 HPLC runs).

Ligand blotting of IGFBPs. Ligand blots for individual IGFBP were performed using all individual plasma samples available for saline- and betamethasone-treated fetuses at 121–122 and 132–133 dG, and saline- and betamethasone-treated postnatal progeny at 42 and 84 days of age. A similar ligand blot was performed using plasma pooled within groups and ages, for saline and betamethasone-exposed fetuses at 109, 116, 122–3, 132–3, and 145–7 dG and lambs at 42 and 84 days postnatal age. Plasma samples (20 µl of a 1:10 dilution) were heated to 65°C for 20 min and then subjected to nonreducing discontinuous SDS-PAGE on a 4.4% stacking gel and 10% separating gel. Proteins were electrotransferred to 0.2 µm nitrocellulose and air-dried overnight, and IGFBP was detected by Western blotting with 125I-IGF-II (25). IGFBP bands were visualized by exposing membranes to phosphorimager screens at room temperature for ~21 days. 14C protein molecular weight markers (Rainbow 14C methylated protein markers; Amersham Life Science) and a nonpregnant sheep QC plasma, prepared as above, were included in each gel. Phosphorimager screens were scanned (Typhoon Trio+ scanner; GE Healthcare) and analyzed densitometrically using Quantity One software (Bio-Rad), and the density of each band was expressed relative to the mean density of the two IGFBP-3 bands in the nonpregnant ewe QC plasma. IGFBP bands present in ovine plasma have been previously identified as IGFBP-3 (42- to 50-kDa doublet), IGFBP-2 (33 kDa), IGFBP-1 (~28 kDa), and IGFBP-4 (24 kDa) (7, 8, 24).

Statistical analyses. Effects of gestational and postnatal age on circulating IGF and total IGFBP in control animals were analyzed by one-way ANOVA. Effects of betamethasone on fetal weight, plasma IGF, total IGFBP abundance, and IGFBP concentrations were analyzed by one-way ANOVA after one, two, and three doses of betamethasone. Effects of age and betamethasone exposure on body weight and circulating IGF and total IGFBP abundance were also analyzed separately in all fetuses after three betamethasone exposures (i.e., at 121–122, 132–133, and 146–147 dG) and in all postnatal animals (at 42 and 84 days postnatal age) by two-way ANOVA. Differences in total IGFBP abundance were observed at 132–133 dG and 84 days postnatal age, but not at 121–122 dG or 42 days postnatal age. The effects of betamethasone exposure on abundances of individual IGFBP were therefore analyzed separately at each age in fetuses and postnatal progeny at 121–122 and 132–133 dG and 42 and 84 days postnatal age, by one-way ANOVA. Linear regression analysis was used to test the a priori hypothesis that plasma IGF-I and IGFBP concentrations would positively predict fetal and placental weights. Analyses were performed using SPSS for Windows version 13.0 (SPSS, Chicago, IL), and data are presented as means ± SE unless indicated otherwise. Differences of P < 0.05 were accepted as statistically significant, with P < 0.1 as a trend.


   RESULTS
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 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
DISCUSSION
 GRANTS
 REFERENCES
 
Fetal and postnatal weight. Fetal weight at 109 dG was not reduced after one injection of betamethasone to the mother (P = 0.9), compared with fetuses of saline-injected ewes (Fig. 1A). At 116 dG, however, fetuses whose mothers had received two betamethasone injections were lighter (P = 0.022) than those whose mothers had received two injections of saline (Fig. 1A). Similarly, three maternal injections with betamethasone reduced fetal weight at 122–123 dG (P = 0.006), and this persisted to 132–133 dG (P = 0.028), and tended to at 145–147 dG (P = 0.059, Fig. 1A). Between 122–123 dG and 145–147 dG, after three maternal doses of betamethasone or saline, fetal weight increased with increasing gestational age (P < 0.001) but was reduced by maternal betamethasone treatment (P < 0.001). A maternal course of three betamethasone injections did not change progeny weight at 42 days (P = 0.33) or 84 days (P = 0.17) of postnatal age (Fig. 1B).


Figure 1
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  		Fig. 1. Body weight of fetuses (A) and progeny (B) of ewes treated with saline (control, unfilled circles) or one (filled circles), two (filled squares), or three (filled triangle) doses of betamethasone during pregnancy. Gestational time points of betamethasone administration are indicated by shaded arrows. Data are means ± SE, and the effect of treatment at each age is indicated as follows: #P < 0.1, *P < 0.05, and **P < 0.01.

 
Fetal and postnatal plasma IGF-I and -II. Plasma IGF-I concentrations increased with gestational age in control fetuses between 75 and 146 dG (P < 0.001, Fig. 2A). Fetal plasma IGF-I was not reduced after one or two maternal betamethasone injections (109 dG: P = 0.95; d116: P = 0.27, Fig. 2A). Exposure to three maternal betamethasone injections did not alter fetal plasma IGF-I at 122–123 dG (P = 0.204) or near term at 145–147 dG (P = 0.226) but reduced fetal plasma IGF-I at 132–133 dG (P = 0.008, Fig. 2A). Between 122–123 dG and 145–147 dG, two-way ANOVA indicated that fetal plasma IGF-I did not change with gestational age but was reduced by maternal betamethasone treatment (P = 0.004, Fig. 2A). Maternal betamethasone treatment did not affect plasma IGF-I in 42-day-old progeny (P = 0.93) but reduced plasma IGF-I in 84-day-old progeny (P = 0.012, Fig. 2B).


Figure 2
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  		Fig. 2. Plasma insulin-like growth factor (IGF)-I (A and B), IGF-II (C and D), and total IGF-binding protein (IGFBP; E and F) concentrations in fetuses (A, C, and E) and progeny (B, D, and F) of ewes treated with saline (control, unfilled circles) or one (filled circles), two (filled squares), or three (filled triangle) doses of betamethasone during pregnancy. Gestational time points of betamethasone administration are indicated by shaded arrows. Data are means ± SE, and the effect of treatment at each age is indicated as follows: #P < 0.1, *P < 0.05, and **P < 0.01.

 
Plasma IGF-II concentrations changed with gestational age in control fetuses (P < 0.001), increasing up to 121–122 dG and then decreasing to term (Fig. 2C). Fetal plasma IGF-II tended to increase at 109 dG after one maternal betamethasone injection (P = 0.069), but exposure to two or three maternal betamethasone injections did not alter fetal plasma IGF-II later in gestation (P > 0.5 for each, Fig. 2C). Between 122–123 dG and 145–147 dG, two-way ANOVA indicated that fetal plasma IGF-II decreased with increasing gestational age (P = 0.006) and was not changed by maternal betamethasone treatment (P > 0.5, Fig. 2C). Maternal betamethasone treatment did not alter plasma IGF-II in 42-day-old (P = 0.998, Fig. 2D) or 84-day-old progeny (P = 0.210, Fig. 2D).

Fetal and postnatal plasma IGFBPs. Plasma total IGFBP concentrations increased with gestational age in control fetuses (P = 0.021, Fig. 2E). Fetal plasma total IGFBP was not reduced after one or two maternal betamethasone injections (109 dG: P = 0.59; d116: P = 0.51, Fig. 2E). Exposure to three maternal betamethasone injections did not alter fetal plasma total IGFBP at 122–123 dG (P = 0.637) or near term at 145–147 dG (P = 0.355) but reduced fetal plasma total IGFBP at 132–133 dG (P = 0.015, Fig. 2E). Between 122–123 dG and 145–147 dG, two-way ANOVA indicated that fetal plasma total IGFBP decreased with increasing gestational age (P = 0.049) and was reduced by maternal betamethasone treatment (P = 0.026, Fig. 2E). Maternal betamethasone treatment did not alter plasma total IGFBP in 42-day-old progeny (P = 0.87) but tended to reduce plasma total IGFBP in 84-day-old progeny (P = 0.088, Fig. 2F).

Western ligand blots of fetal and postnatal plasma using 125I-IGF-II as ligand exhibited five bands (Fig. 3) : from top, a doublet of two bands at 42–50 kDa (IGFBP-3), a single band at 33 kDa (IGFBP-2), and fainter bands at ~28 (IGFBP-1) and ~24 (IGFBP-4) kDa. On the basis of apparent differences in IGFBP-3 and IGFBP-2 abundances apparent in plasma pools at each age (Fig. 3), we then analyzed IGFBP abundance in individual plasma samples from fetuses at 121–122 dG and 132–133 dG and in postnatal progeny at 42 and 84 days age. Limited sample volumes precluded further analysis in fetuses at 146 dG. As expected, the relative abundance of IGFBP-2 in plasma was higher in the fetus than postnatally (Fig. 4). The abundance of plasma IGFBP-3 at 84 d postnatal age was reduced (P = 0.016) in progeny whose mothers had received three doses of betamethasone during pregnancy, compared with progeny of saline-treated ewes (Fig. 4). Maternal betamethasone treatment did not alter plasma abundance of individual IGFBPs in fetuses, or at 42 d postnatal age (Fig. 4).


Figure 3
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  		Fig. 3. Western ligand blot of IGFBP in plasma pools from fetuses and progeny of ewes treated with saline (control, C) or betamethasone (B). Age of fetuses is shown in days of gestation (dG), and age of postnatal progeny is shown in days (d). Plasma from a nonpregnant ewe (NPE QC) was run as a quality control sample in each gel.

 

Figure 4
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  		Fig. 4. Plasma abundance of individual IGFBPs in fetuses at 121–122 (A) and 132–133 (B) dG and at 42 (C) and 84 (D) days postnatal age in fetuses and progeny of ewes treated with saline (control, open bars) or three (filled bars) doses of betamethasone during pregnancy. Data are means ± SE, and the effect of treatment at each age is indicated as follows: *P < 0.05.

 
Relationships between growth and the IGF axis. Fetal and placental weights did not correlate with plasma IGF-I, IGF-II, or total IGFBP concentrations at 109 dG after administration of one dose of saline or betamethasone to the mother (P > 0.26 for all). At 116 dG, after administration of two doses of saline or betamethasone to the mother, fetal weight tended to correlate positively with fetal plasma total IGFBP, and placental weight correlated positively with fetal plasma IGF-I (Fig. 5). At 121–122 dG, after administration of three doses of saline or betamethasone to the mother, fetal weight correlated positively with fetal plasma IGF-I (Fig. 5). Placental weight at 121 dG correlated positively with fetal plasma IGF-I, IGF-II, and IGFBP (Fig. 5). At 132–133 dG, fetal weight correlated positively with fetal plasma IGF-I and total IGFBP (Fig. 5). At 145–147 dG, fetal weight correlated positively with fetal plasma IGF-II. Placental weights at 132–133 and 145–147 dG did not correlate with fetal plasma IGF or IGFBP concentrations (Fig. 5). Postnatally, progeny body weight at 42 days of age correlated positively with plasma IGF-I, IGF-II, and total IGFBP, whereas body weight at 84 days of age correlated positively with plasma IGF-II (Fig. 6).


Figure 5
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  		Fig. 5. Plasma IGF and IGFBP abundances predict fetal and placental weights. Relationships between fetal plasma IGF-I (A, D, G, and K), IGF-II (B, E, H, and L), and total IGFBP (C, F, I, and M), and fetal (circles) and placental (squares) weights at 116 dG (A–C), 121–122 dG (D–F), 132–133 dG (G–I), and 145–147 dG (K–M). Fetuses from saline-treated ewes are shown by open symbols, and fetuses from betamethasone-treated ewes are shown by filled symbols. Significant correlations (P < 0.05) are indicated by solid lines, and trends (P < 0.1) are indicated by dashed lines.

 

Figure 6
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  		Fig. 6. Plasma IGF and IGFBP abundances predict progeny body weight after birth. Relationships between progeny plasma IGF-I (A), IGF-II (B), and total IGFBP (C), and progeny body weight at 42 days postnatal age (circles) and 84 days postnatal age (squares). Progeny of saline-treated ewes are shown by open symbols, and progeny of betamethasone-treated ewes are shown by filled symbols. Significant correlations (P < 0.05) are indicated by solid lines, and trends (P < 0.1) are indicated by dashed lines.

 

   DISCUSSION
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
GRANTS
 REFERENCES
 
Repeated administration of betamethasone to the mother programs the IGF axis in the fetus and progeny. We have shown, for the first time in any species, that exposure to synthetic glucocorticoids before birth programs or causes persistent changes in the IGF axis before and after birth. Injecting the pregnant ewe with betamethasone once per week for 3 wk from ~0.7 of term to 0.8 of term decreased plasma IGF-I and total IGFBP concentrations in fetuses after the third injection. Plasma IGF-I and total IGFBP were not decreased in plasma collected from fetuses shortly after the first or second maternal injections with betamethasone, although longer-term responses cannot be excluded. The present study was designed to compare long-term effects of three repeated betamethasone exposures, rather than fewer exposures, since we have previously shown that this treatment regimen suppresses fetal and progeny growth in sheep, whereas single doses do not (6, 39–41, 51). Betamethasone did not alter circulating concentrations of IGF or IGFBP at 42 days postnatal age, when any effects of glucocorticoid exposure were hidden by the large interanimal variation in circulating IGF-I and IGFBP. Importantly, however, suppression of IGF-I and total IGFBP abundance after three maternal doses of betamethasone was apparent at 84 days of postnatal age in the present study. The suppression of fetal plasma IGF-I and IGFBP after exposure to repeated glucocorticoids contrasts with the changes reported by Kajantie et al. (29) in cord blood collected from preterm human infants, who reported increasing IGF-I and IGFBP-3 with increasing number of antenatal betamethasone treatments. Whether this reflects additional stresses associated with preterm birth or species differences is not clear. In addition, pregnant ewes in the present study were treated with progesterone to prevent preterm labor, although this cotreatment is not routine in women treated with betamethasone, and it is possible that progesterone might modify effects of subsequent repeated betamethasone exposure. The effects of repeated exposure to synthetic glucocorticoids on fetal plasma IGF-I contrast with known effects of chronically elevated endogenous glucocorticoid (cortisol), which increases hepatic IGF-I mRNA expression but does not alter plasma IGF-I (34). Given the lack of IGF-I suppression in response to cortisol, we suggest that effects of repeated betamethasone on fetal plasma IGF-I abundance may be indirect and may be a consequence of betamethasone-induced reductions in placental growth and function (6), and possibly nutrient transport, and that this may contribute to persistence of reduced plasma IGF-I abundance to term. Reduced fetal plasma IGF-I concentrations are thus a common feature of several models of fetal growth restriction in the sheep, including surgical restriction of placental growth (43), acute maternal alcohol consumption (22), severe maternal undernutrition (5), and in the present study, repeated in utero exposure to the synthetic glucocorticoid betamethasone.

The most important finding of this study is that suppression of circulating IGF-I and total IGFBP abundance following in utero exposure to repeated courses of betamethasone persisted postnatally at 84 days of age, ~110 days after the final betamethasone injection. Suppression of plasma total IGFBP concentrations in the postnatal lambs paralleled that of IGFBP-3 specifically. Circulating IGFBPs prolong the half-life of IGFs in circulation but appear to decrease their bioavailability to receptors (19). In the present study, the magnitude of betamethasone-induced decreases in plasma IGF-I and total IGFBP or IGFBP-3 in 84-day-old progeny were similar, however, implying that the ratio of IGF to IGFBP in circulation, and thus its bioavailability, would not be changed. Decreased circulating IGFBP might, however, contribute to decreased circulating IGF-I by decreasing its half-life in circulation. To our knowledge, this is the first study to report that prenatal glucocorticoid exposure programs the IGF axis beyond the neonatal period. It is possible that glucocorticoid exposure has caused epigenetic changes in the IGF-I and IGFBP genes or their upstream promotors in a manner that persistently downregulated their expression. Effects of glucocorticoids on DNA methylation or on covalent modifications of histones on IGF and IGFBP gene loci have not been reported, but histones of the hepatic IGF-I locus are epigenetically modified in a rat model of IUGR, a model that is characterized by elevated endogenous glucocorticoids (4, 21). Indeed, glucocorticoid exposure of rat heptocytes in vivo induces differential demethylation of glucocorticoid responsive units within the promoter region of the tyrosine aminotransferase gene (54). Furthermore, demethylation of the Tat promoter persisted for at least 3 mo following glucocorticoid removal and increased subsequent glucocorticoid induction of the gene (54), demonstrating that glucocorticoids can induce persistent changes in gene expression through epigenetic mechanisms.

Plasma IGF-II tended to be increased transiently after the first betamethasone injection but was not altered following repeated maternal treatment with betamethasone, and postnatal plasma IGF-II abundance was not altered by prenatal betamethasone exposure. IGF-II expression in liver and muscle of late-gestation fetal sheep is downregulated by chronic exposure to cortisol (35), but our results imply that the synthetic glucocorticoid betamethasone does not downregulate expression of this gene.

Repeated glucocorticoid exposure: Consequences for prenatal and postnatal growth. Fetal growth was reduced after administration of repeated doses of betamethasone to the mother, and this persisted to term, as previously reported for this cohort (6). Effects on postnatal growth were not significant in the present cohort, most likely due to the limited animal numbers. In previous studies, however, weight of postnatal sheep progeny was reduced at 2–3 mo of age and normalized by 6 mo of age and in adults (39, 41). In humans, exposure to repeated glucocorticoids in utero reduces size at birth or increases risk of SGA (small for gestational age), particularly with increasing numbers of repeated courses (9, 11). In a recent RCT, repeat glucocorticoids did not affect growth up to two years of age, although at the doses used, birth weight was also not affected (10). Further follow-up studies of infants from existing randomized trials of repeat glucocorticoids, especially where higher doses have been used, may be warranted.

Consequences of glucocorticoid programming of the IGF axis. We have now shown that repeated in utero exposure to synthetic glucocorticoids at ~0.7 to 0.8 of gestation in normally grown fetuses suppresses fetal, placental, and early postnatal growth (6, 26, 39, 41) and is associated with markers of insulin resistance and with altered capacity for hepatic glucose metabolism up to adulthood (41, 50). It also increases fetal plasma ACTH levels up to term (51), induces pituitary-adrenal hyperresponsiveness in young adult sheep at 1 yr of age, followed by adrenal hyporesposiveness at 3 yr of age (49), and, as reported here, programs the IGF axis before and after birth in the sheep. In the present study, fetal and placental weights correlated positively with plasma IGF-I and total IGFBP, at some, but not all, ages; however, in all cases the direction of the relationship was positive, and programming of decreased IGF abundance may contribute to suppression of fetal growth following repeated exposure to maternal betamethasone. Positive correlations between IGF and IGFBP abundance and weights were far more consistent in postnatal progeny, providing stronger evidence that betamethasone exposure impairs postnatal growth through its actions on this axis. Insulin action may be particularly susceptible to programming by glucocorticoids; we have shown that a brief exposure to dexamethasone in early gestation programs increased insulin sensitivity of lipid metabolism in adult female offspring (23), and improved glucose tolerance in conjunction with increased first-phase glucose-stimulated insulin secretion in adult male offspring (13). It is possible that in utero programming of insulin action may occur at least in part via programming of the IGF axis, since low plasma IGF-I predicts later development of impaired glucose tolerance, type 2 diabetes, and cardiovascular disease in adults (17). The role of the IGF axis in mediating programming of postnatal metabolism by endogenous glucocorticoids merits further investigation.

Glucocorticoid programming of the IGF axis may also contribute to growth restriction during and after IUGR. The IUGR fetus is exposed to elevated glucocorticoids of maternal and fetal origin and has reduced protection from maternal glucocorticoids due to decreased placental expression of the glucocorticoid-inactivating enzyme 11β-hydroxysteroid dehydrogenase-2 (28, 48). Consistent with the current findings that repeated glucocorticoid exposure reduces circulating IGF abundance before and after birth, the IUGR fetus is characterized by reduced circulating IGFs before and after birth (14, 18, 30, 32, 33). The degree of comorbidity between premature delivery and fetal growth restriction means that many babies who are delivered prematurely and exposed to glucocorticoids are also growth restricted (11). The effects of increased exposure to endogenous glucocorticoids on the IGF axis in IUGR, and hence on the long-term growth and metabolic consequences, may be exacerbated by exposure to betamethasone.

Conclusions

We conclude that repeated maternal betamethasone treatment reduces the abundance of circulating IGF-I and IGFBP in fetal plasma, which persists into early postnatal life. This reduction in plasma IGF-I may contribute to the previously reported reductions in fetal and early postnatal growth and impairment of metabolic function following repeated exposure to elevated synthetic glucocorticoids in the sheep, and possibly in other species.


   GRANTS
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 GRANTS
REFERENCES
 
This study was supported by the Raine Medical Foundation of Western Australia, The Child Health Research Foundation of WA, and the National Health and Medical Research Council (NHMRC) of Australia. K. L. Gatford held the Hilda Farmer Medical Research Associateship of the University of Adelaide. T. J. M. Moss held a Biomedical Career Development Award (303261) from the NHMRC. D. M. Sloboda was the Forrest Fetal Research Scientist of the Women and Infants Research Foundation, Western Australia.


   ACKNOWLEDGMENTS
 
We thank Dr. Ilias Nitsos and Adrian Jonker for assistance in the postmortems.

Current addresses of D. M. Sloboda: The Liggins Institute, University of Auckland, Private Bag 92019, Auckland, New Zealand; and T. J. M. Moss: Dept. of Physiology, Monash University, Clayton Vic 3800, Australia.


   FOOTNOTES
 

Address for reprint requests and other correspondence: K. L. Gatford, Research Centre for Early Origins of Adult Disease, Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, Univ. of Adelaide SA 5005, Australia (e-mail: kathy.gatford{at}adelaide.edu.au)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


   REFERENCES
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 GRANTS
 REFERENCES
 

  1. Ahmad I, Beharry KDA, Valencia AM, Cho S, Guajardo L, Nageotte MP, Modanlou HD. Influence of a single course of antenatal betamethasone on the maternal-fetal insulin-IGF-GH axis in singleton pregnancies. Growth Horm IGF Res 16: 267–275, 2006.[CrossRef][Web of Science][Medline]
  2. Ain R, Canham LN, Soares MJ. Dexamethasone-induced intrauterine growth restriction impacts the placental prolactin family, insulin-like growth factor-II and the Akt signaling pathway. J Endocrinol 185: 253–263, 2005.[Abstract/Free Full Text]
  3. Baker J, Liu JP, Robertson EJ, Efstratiadis A. Role of insulin-like growth factors in embryonic and postnatal growth. Cell 75: 73–82, 1993.[CrossRef][Web of Science][Medline]
  4. Baserga M, Hale MA, McKnight RA, Yu X, Callaway CW, Lane RH. Uteroplacental insufficiency alters hepatic expression, phosphorylation, and activity of the glucocorticoid receptor in fetal IUGR rats. Am J Physiol Regul Integr Comp Physiol 289: R1348–R1353, 2005.[Abstract/Free Full Text]
  5. Bauer MK, Breier BH, Harding JE, Veldhuis JD, Gluckman PD. The fetal somatotropic axis during long-term maternal undernutrition in sheep: evidence for nutritional regulation in utero. Endocrinology 136: 1250–1257, 1995.[Abstract]
  6. Braun T, Li S, Moss TJM, Newnham JP, Challis JRG, Gluckman PD, Sloboda DM. Maternal betamethasone administration reduces binucleate cell number and placental lactogen in sheep. J Endocrinol 194: 337–347, 2007.[Abstract/Free Full Text]
  7. Carr JM, Grant PA, Francis GL, Owens JA, Wallace JC, Walton PE. Isolation and characterization of ovine IGFBP-4: protein purification and cDNA sequence. J Mol Endocrinol 13: 219–236, 1994.[Abstract/Free Full Text]
  8. Carr JM, Owens JA, Grant PA, Walton PE, Owens PC, Wallace JC. Circulating insulin-like growth factors (IGFs), IGF-binding proteins (IGFBPs) and tissue mRNA levels of IGFBP-2 and IGFBP-4 in the ovine fetus. J Endocrinol 145: 545–557, 1995.[Abstract/Free Full Text]
  9. Crowther C, Harding J. Repeat doses of prenatal corticosteroids for women at risk of preterm birth for preventing neonatal respiratory disease. Cochr Database Syst Rev 3: CD003935, 2007.
  10. Crowther CA, Doyle LW, Haslam RR, Hiller JE, Harding JE, Robinson JS, the ASG. Outcomes at 2 years of age after repeat doses of antenatal corticosteroids. N Engl J Med 357: 1179–1189, 2007.[Abstract/Free Full Text]
  11. Crowther CA, Haslam RR, Hiller JE, Doyle LW, Robinson JS. Neonatal respiratory distress syndrome after repeat exposure to antenatal corticosteroids: a randomised controlled trial. Lancet 367: 1913–1919, 2006.[CrossRef][Web of Science][Medline]
  12. Dalziel SR, Walker NK, Parag V, Mantell C, Rea HH, Rodgers A, Harding JE. Cardiovascular risk factors after antenatal exposure to betamethasone: 30-year follow-up of a randomised controlled trial. Lancet 365: 1856–1862, 2005.[CrossRef][Web of Science][Medline]
  13. De Blasio MJ, Dodic M, Jefferies AJ, Moritz KM, Wintour EM, Owens JA. Maternal exposure to dexamethasone or cortisol in early pregnancy differentially alters insulin secretion and glucose homeostasis in adult male sheep offspring. Am J Physiol Endocrinol Metab 293: E75–E82, 2007.[Abstract/Free Full Text]
  14. de Waal WJ, Hokken-Koelega ACS, Stijnen T, de Muinck Keizer-Schrama SMPF. Endogenous and stimulated GH secretion, urinary GH excretion, and plasma IGF-I and IGF-II levels in prepubertal children with short stature after intrauterine growth retardation. Clin Endocrinol (Oxf) 41: 621–630, 1994.[Medline]
  15. DeChiara TM, Efstratiadis A, Robertson EJ. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345: 78–80, 1990.[CrossRef][Medline]
  16. Duncombe GJ, Barker AP, Moss TJM, Gurrin LC, Charles AK, Smith NM, Newnham JP. The effects of overcoming experimental bladder outflow obstruction in fetal sheep. J Mater-Fetal Neonat Med 11: 130–137, 2002.
  17. Dunger D, Yuen K, Ong K. Insulin-like growth factor I and impaired glucose tolerance. Horm Res 62, Suppl 1: 101–107, 2004.[CrossRef][Web of Science][Medline]
  18. Fall CHD, Pandit AN, Law CM, Yajnik CS, Clark PM, Breier B, Osmond C, Shiell AW, Gluckman PD, Barker DJP. Size at birth and plasma insulin-like growth factor-1 concentrations. Arch Dis Childhood 73: 287–293, 1995.[Abstract/Free Full Text]
  19. Firth SM, Baxter RC. Cellular actions of the insulin-like growth factor binding proteins. Endocr Rev 23: 824–854, 2002.[Abstract/Free Full Text]
  20. Francis GL, Owens PC, McNeil KA, Wallace JC, Ballard FJ. Purification, amino acid sequences and assay cross-reactivities of porcine insulin-like growth factor-I and -II. J Endocrinol 122: 681–687, 1989.[Abstract/Free Full Text]
  21. Fu Q, McKnight RA, Yu X, Men P, Lane RH. Intrauterine growth restriction alters histone code along the rat hepatic insulin-like growth factor 1 locus. J Investig Med 55: S89–S89, 2007.[CrossRef]
  22. Gatford KL, Dalitz PA, Cock ML, Harding R, Owens JA. Acute ethanol exposure in pregnancy alters the insulin-like growth factor axis of fetal and maternal sheep. Am J Physiol Endocrinol Metab 292: E494–E500, 2007.[Abstract/Free Full Text]
  23. Gatford KL, Wintour EM, De Blasio MJ, Owens JA, Dodic M. Differential timing for programming of glucose homeostasis, metabolic sensitivity to insulin and blood pressure by in utero exposure to dexamethasone in sheep. Clin Sci 98: 553–560, 2000.[CrossRef][Web of Science][Medline]
  24. Hooper SB, Bocking AD, White SE, Fraher LJ, McDonald TJ, Han VK. Catecholamines stimulate the synthesis and release of insulin-like growth factor binding protein-1 (IGFBP-1) by fetal sheep liver in vivo. Endocrinology 134: 1104–1112, 1994.[Abstract/Free Full Text]
  25. Hossenlopp P, Seurin D, Segovia-Quinson B, Hardouin S, Binoux M. Analysis of serum insulin-like growth factor binding proteins using western blotting: use of the method for titration of the binding proteins and competitive binding studies. Anal Biochem 154: 138–143, 1986.[CrossRef][Web of Science][Medline]
  26. Ikegami M, Jobe Alan H, Newnham J, Polk Daniel H, Willet Karen E, Sly P. Repetitive prenatal glucocorticoids improve lung function and decrease growth in preterm lambs. Am J Respir Crit Care Med 156: 178–184, 1997.[Abstract/Free Full Text]
  27. Jobe AH, Wada N, Berry LM, Ikegami M, Ervin MG. Single and repetitive maternal glucocorticoid exposures reduce fetal growth in sheep. Am J Obstet Gynecol 178: 880–885, 1998.[CrossRef][Web of Science][Medline]
  28. Kajantie E, Dunkel L, Turpeinen U, Stenman UH, Wood PJ, Nuutila M, Andersson S. Placental 11β-hydroxysteroid dehydrogenase-2 and fetal cortisol/cortisone shuttle in small preterm infants. J Clin Endocrinol Metab 88: 493–500, 2003.[Abstract/Free Full Text]
  29. Kajantie E, Hytinnanti T, Koistinen R, Risteli J, Rutanen EM, Seppala M, Andersson S. Markers of type I and type III collagen turnover, insulin-like growth factors, and their binding proteins in cord plasma of small premature infants: relationships with fetal growth, gestational age, preeclampsia, and antenatal glucocorticoid treatment. Pediatr Res 49: 481–489, 2001.[Web of Science][Medline]
  30. Lassarre C, Hardouin S, Daffos F, Forestier F, Frankenne F, Binoux M. Serum insulin-like growth factors and insulin-like growth factor binding proteins in the human fetus. Relationships with growth in normal subjects and in subjects with intrauterine growth retardation. Pediatr Res 29: 219–225, 1991.[Web of Science][Medline]
  31. Lee BH, Stoll BJ, McDonald SA, Higgins RD, National Institute of Child Health, and Human Development Neonatal Research Network. Neurodevelopmental outcomes of extremely low birth weight infants exposed prenatally to dexamethasone versus betamethasone. Pediatrics 121: 289–296, 2008.[Abstract/Free Full Text]
  32. Leger J, Noel M, Limal JM, Czernichow P. Growth factors and intrauterine growth retardation. II. Serum growth hormone, insulin-like growth factor (IGF) I, and IGF-binding protein 3 levels in children with intrauterine growth retardation compared with normal control subjects: Prospective study from birth to two years of age. Pediatr Res 40: 101–107, 1996.[Web of Science][Medline]
  33. Leger J, Oury JF, Noel M, Baron S, Benali K, Blot P, Czernichow P. Growth factors and intrauterine growth retardation. I. Serum growth hormone, insulin-like growth factor (IGF)-I, IGF-II, and IGF binding protein 3 levels in normally grown and growth-retarded human fetuses during the second half of gestation. Pediatr Res 40: 94–100, 1996.[Web of Science][Medline]
  34. Li J, Owens JA, Owens PC, Saunders JC, Fowden AL, Gilmour RS. The ontogeny of hepatic growth hormone receptor and insulin-like growth factor I gene expression in the sheep fetus during late gestation: developmental regulation by cortisol. Endocrinology 137: 1650–1657, 1996.[Abstract]
  35. Li J, Saunders JC, Gilmour RS, Silver M, Fowden AL. Insulin-like growth factor-II messenger ribonucleic acid expression in fetal tissues of the sheep during late gestation: effects of cortisol. Endocrinology 132: 2083–2089, 1993.[Abstract/Free Full Text]
  36. McLaughlin KJ, Crowther CA, Walker N, Harding JE. Effects of a single course of corticosteroids given more than 7 days before birth: a systematic review. Austr NZ J Obstet Gynaecol 43: 101–106, 2003.[CrossRef]
  37. Mildenhall LFJ, Battin MR, Morton SMB, Bevan C, Kuschel CA, Harding JE. Exposure to repeat doses of antenatal glucocorticoids is associated with altered cardiovascular status after birth. Arch Dis Child Fetal Neonatal Ed 91: F56–F60, 2006.[Abstract/Free Full Text]
  38. Mosier HDJ, Spencer EM, Dearden LC, Jansons RA. The effect of glucocorticoids on plasma insulin-like growth factor I concentration in the rat fetus. Pediatr Res 22: 92–95, 1987.[Web of Science][Medline]
  39. Moss TJM, Doherty DA, Nitsos I, Sloboda DM, Harding R, Newnham JP. Effects into adulthood of single or repeated antenatal corticosteroids in sheep. Am J Obstet Gynecol 192: 146–152, 2005.[CrossRef][Web of Science][Medline]
  40. Moss TJM, Nitsos I, Harding R, Newnham JP. Differential effects of maternal and fetal betamethasone injections in late-gestation fetal sheep. J Soc Gynecol Investig 10: 474–479, 2003.[CrossRef][Web of Science][Medline]
  41. Moss TJM, Sloboda DM, Gurrin LC, Harding R, Challis JRG, Newnham JP. Programming effects in sheep of prenatal growth restriction and glucocorticoid exposure. Am J Physiol Regul Integr Comp Physiol 281: R960–R970, 2001.[Abstract/Free Full Text]
  42. National Institutes of Health Consensus Development Panel. Antenatal corticosteroids revisited: repeat courses-National Institutes of Health Consensus Development Conference Statement, August 17–18, 2000. Obstet Gynecol 98: 144–150, 2001.[CrossRef][Web of Science][Medline]
  43. Owens JA, Kind KL, Carbone F, Robinson JS, Owens PC. Circulating insulin-like growth factors-I and -II and substrates in fetal sheep following restriction of placental growth. J Endocrinol 140: 5–13, 1994.[Abstract/Free Full Text]
  44. Owens PC, Johnson RJ, Campbell RG, Ballard FJ. Growth hormone increases insulin-like growth factor (IGF-I) and decreases IGF-II in plasma of growing pigs. J Endocrinol 124: 269–275, 1990.[Abstract/Free Full Text]
  45. Price WA, Stiles AD, Moats-Staats BM, D'Ercole AJ. Gene expression of insulin-like growth factors (IGFs), the type 1 IGF receptor, and IGF-binding proteins in dexamethasone-induced fetal growth retardation. Endocrinology 130: 1424–1432, 1992.[Abstract/Free Full Text]
  46. Quinlivan JA, Evans SF, Dunlop SA, Beazley LD, Newnham JP. Use of corticosteroids by Australian obstetricians: a survey of clinical practice. Aust NZ J Obstet Gynaecol 38: 1–7, 1998.[Web of Science][Medline]
  47. Roberts D, Dalziel S. Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Cochr Database Syst Rev 3: CD004454, 2006.
  48. Shams M, Kilby MD, Somerset DA, Howie AJ, Gupta A, Wood PJ, Afnan M, Stewart PM. 11β-Hydroxysteroid dehydrogenase type 2 in human pregnancy and reduced expression in intrauterine growth restriction. Hum Reprod 13: 799–804, 1998.[Abstract/Free Full Text]
  49. Sloboda DM, Moss TJM, Li S, Doherty D, Nitsos I, Challis JRG, Newnham JP. Prenatal betamethasone exposure results in pituitary-adrenal hyporesponsiveness in adult sheep. Am J Physiol Endocrinol Metab 292: E61–E70, 2007.[Abstract/Free Full Text]
  50. Sloboda DM, Moss TJM, Li S, Doherty DA, Nitsos I, Challis JRG, Newnham JP. Hepatic glucose regulation and metabolism in adult sheep: effects of prenatal betamethasone. Am J Physiol Endocrinol Metab 289: E721–E728, 2005.[Abstract/Free Full Text]
  51. Sloboda DM, Newnham JP, Challis JR. Effects of repeated maternal betamethasone administration on growth and hypothalamic-pituitary-adrenal function of the ovine fetus at term. J Endocrinol 165: 79–91, 2000.[Abstract]
  52. Sloboda DM, Newnham JP, Challis JR. Repeated maternal glucocorticoid administration and the developing liver in fetal sheep. J Endocrinol 175: 535–543, 2002.[Abstract]
  53. Thakur A, Sase M, Lee JJ, Thakur V, Buchmiller TL. Effect of dexamethasone on insulin-like growth factor-1 expression in a rabbit model of growth retardation. J Pediatr Surg 35: 898–905, 2000.[CrossRef][Web of Science][Medline]
  54. Thomassin H, Flavin M, Espinás ML, Grange T. Glucocorticoid-induced DNA demethylation and gene memory during development. EMBO J 20: 1974–1983, 2001.[CrossRef][Web of Science][Medline]
  55. Verhaeghe J, Van Herck E, Billen J, Moerman P, Van Assche FA, Giudice LC. Regulation of insulin-like growth factor-I and insulin-like growth factor binding protein-1 concentrations in preterm fetuses. Am J Obstet Gynecol 188: 485–491, 2003.[CrossRef][Web of Science][Medline]
  56. Woodall SM, Breier BH, Johnston BM, Gluckman PD. A model of intrauterine growth retardation caused by chronic maternal undernutrition in the rat: effects on the somatotrophic axis and postnatal growth. J Endocrinol 150: 231–242, 1996.[Abstract/Free Full Text]
  57. Yuen KCJ, Dunger DB. Impact of treatment with recombinant human GH and IGF-I on visceral adipose tissue and glucose homeostasis in adults. Growth Horm IGF Res 16: 55–61, 2006.[CrossRef]



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