Open Access

Rescue of glucocorticoid-programmed adipocyte inflammation by omega-3 fatty acid supplementation in the rat

  • Peter J Mark1Email author,
  • Caitlin S Wyrwoll1,
  • Intan S Zulkafli1,
  • Trevor A Mori2 and
  • Brendan J Waddell1
Reproductive Biology and Endocrinology201412:39

https://doi.org/10.1186/1477-7827-12-39

Received: 6 December 2013

Accepted: 26 April 2014

Published: 13 May 2014

Abstract

Background

Adverse fetal environments predispose offspring to pathologies associated with the metabolic syndrome. Previously we demonstrated that adult offspring of dexamethasone-treated mothers had elevated plasma insulin and pro-inflammatory cytokines, effects prevented by a postnatal diet enriched with omega (n)-3 fatty acids. Here we tested whether prenatal glucocorticoid excess also programmed the adipose tissue phenotype, and whether this outcome is rescued by dietary n-3 fatty acids.

Methods

Offspring of control and dexamethasone-treated mothers (0.75 μg/ml in drinking water, day 13 to term) were cross-fostered to mothers on a standard (Std) or high n-3 (Hn3) diet at birth. Offspring remained on these diets post-weaning, and serum and retroperitoneal fat were obtained at 6 months of age (n = 5-8 per group). Serum was analysed for blood lipids and fatty acid profiles, adipocyte cross sectional area was measured by unbiased stereological analysis and adipose expression of markers of inflammation, glucocorticoid sensitivity and lipid metabolism were determined by RT-qPCR analysis.

Results

Serum total fatty acid levels were elevated (P < 0.01) in male offspring of dexamethasone-treated mothers, an effect prevented by Hn3 consumption. Prenatal dexamethasone also programmed increased adipose expression of Il6, Il1b (both P < 0.05) and Tnfa (P < 0.001) mRNAs regardless of fetal sex, but again this effect was prevented (for Il6 and Il1b) by Hn3 consumption. Offspring of dexamethasone-treated mothers had increased adipose expression of Gr (P = 0.008) and Ppara (P < 0.05) regardless of sex or postnatal diet, while 11bHsd1 was upregulated in males only. The Hn3 diet increased Ppard expression and reduced adipocyte size in all offspring (both P < 0.05) irrespective of prenatal treatment.

Conclusions

Prenatal glucocorticoid exposure programmed increased expression of inflammatory markers and enhanced glucocorticoid sensitivity of adipose tissue. Partial prevention of this phenotype by high n-3 consumption indicates that postnatal dietary manipulations can limit adverse fetal programming effects on adipose tissue.

Background

The incidence of obesity and related metabolic disorders (hypertension, insulin resistance and dyslipidemia) have risen dramatically in recent decades, with major implications for cardiovascular disease risk [1]. There is growing evidence that a range of insults in early life, including in utero, can developmentally program adverse outcomes for the adult phenotype. Most notably, undernutrition, overnutrition and glucocorticoid excess can all program adverse phenotypic outcomes. Accordingly, offspring born small (a proxy for a poor fetal environment) are predisposed to several adult-onset diseases including diabetes and obesity [2, 3]. We previously demonstrated that offspring of rat mothers treated with dexamethasone during pregnancy were growth retarded at birth and as adults, were hyperleptinemic, hyperinsulinemic and hypertensive [4]. These offspring also exhibited a pro-inflammatory state, with plasma levels of tumor necrosis factor alpha (TNFα), interleukin 6 (IL6) and IL1β all increased by prenatal dexamethasone [5]. Moreover, because this pro-inflammatory state and most other adverse programming outcomes were prevented by postnatal dietary omega (n)-3 fatty acid supplementation, we have proposed that inflammation may be a key driver of the overall programmed phenotype [5]. In particular, adipose tissue inflammation may underlie the programmed pro-inflammatory phenotype, since adipose tissue leptin expression was elevated in offspring that had been exposed prenatally to dexamethasone [4]. To test this hypothesis we characterised the adipose tissue phenotype and serum fatty acid profiles in adult offspring of dexamethasone-treated mothers. Specifically, we measured adipocyte size (by unbiased stereology) and adipose expression of pro-inflammatory cytokines, peroxisome proliferator-activated receptors, and determinants of glucocorticoid sensitivity (i.e., the glucocorticoid receptor (GR; Nr3c1) and 11β-hydroxysteroid dehydrogenase (11bHsd) enzymes). This focus on adipose glucocorticoid sensitivity was considered important given that enhanced glucocorticoid activity in adipocytes appears to be obesogenic (for review see [6]). Moreover, because the programmed phenotype in our model was largely rescued in offspring raised on a diet enriched with n-3 fatty acids [4, 5] we also characterised the adipose phenotype and fatty acid profiles of these offspring.

Methods

Animals and diets

Nulliparous albino Wistar rats aged between 8 and 10 weeks were obtained from the Animal Resources Centre (Murdoch, Australia) and maintained under controlled lighting and temperature as previously described [7]. Two isocaloric, semi-pure diets were used in this study, each formulated with identical ratios of protein, carbohydrate, fat, and salt, but with markedly different n-3 fatty acid contents as previously described [4]. The Hn3 diet contained 34% of total fats as long chain n-3 fatty acids whereas the standard diet contained 0.8% n-3 fatty acids. The semi-pure diets were manufactured by Specialty Feeds (Glen Forrest, Australia) and were sterilized by gamma-irradiation. Ten days before mating, half the females were placed on one of the two semi-pure diets; standard (Std) or high omega-3 fatty acids (Hn3), while the others remained on a normal rat chow (Specialty Feeds, Glen Forrest, Australia). All rats were provided with acidified water and food ad libitum. All procedures involving animals were approved by the Animal Ethics Committee of The University of Western Australia. Rats were mated overnight and the day on which spermatozoa were present in a vaginal smear was designated day 1 of pregnancy. Dexamethasone (Dex) acetate (Sigma Chemical Co., St Louis, MO, USA) was administered in the drinking water (0.75 μg/ml) from day 13 until birth in half of the pregnancies. Previous studies show that dexamethasone acetate administered via maternal drinking water results in consistent, dose-dependent reductions in birth weight [8]. In the current study, birth weight was reduced by 24% and 25% in males and females, respectively, as previously reported [4]. Within 24 h of birth, all pups from control (Con) and Dex-treated mothers were cross-fostered to a mother consuming either a Std diet or Hn3 diet. Cross-fostering resulted in four treatment groups (Con/Std, Con/Hn3, Dex/Std and Dex/Hn3), and pups remained with their foster mothers until weaning, at which point male and female offspring were caged separately and remained on their allocated diets (Std or Hn3).

Tissue collection

At 6 months of age, a male and female were randomly selected from each litter, fasted overnight for 16 h, weighed and anesthetized with 40 mg/kg Nembutal (Rhone Merieux, Pinkenba, Australia). Blood was collected from the dorsal aorta and serum stored at −20°C until subsequent analysis. Retroperitoneal adipose tissue samples were collected and either fixed (Histochoice) or snap frozen in liquid nitrogen and stored at −80°C until analysis.

Measurement of blood lipids

Serum total cholesterol and triacylglycerols were determined enzymatically on a Cobas MIRA analyser (Roche Diagnostics, Basel, Switzerland) with reagents from Trace Scientific (Melbourne, Australia). High density lipoprotein-cholesterol (HDL-C) was determined on a heparin-manganese supernatant [9]. The intra-assay coefficients of variation were 2.2% at 4.2 mM and 1.4% at 10.5 mM for total cholesterol, 1.6% at 4.0 mM and 2.5% at 1.2 mM for triacylglycerols, and 1.9% at 1.1 mM for HDL-C. In each case all samples were measured in a single assay. Serum levels of a range of fatty acids were analysed by gas chromatography as previously described [10]. Briefly, serum (200 μL) was extracted with 2 ml chloroform/methanol (2:1, v/v). Fatty acid methyl esters were prepared by treatment of total lipid extracts with 4% H2SO4 in methanol at 90°C for 20 min and analysed by gas liquid chromatography using a Hewlett-Packard model 5980A gas chromatograph (Hewlett Packard, Rockville, MD). The samples were resolved on a BPX70 column (25 cm × 0.32 mm, 0.25 μm film thickness; SGE, Ringwood, Victoria, Australia) with a temperature program increasing from 150°C to 210°C at 4°C/min and using N2 as the carrier gas at a split ratio of 30:1. Peaks were identified by comparison with a known standard mixture.

Adipose tissue morphometry

Fixed retroperitoneal fat samples (n = 5 per group) from male rats were processed and embedded in paraffin wax. Three sections (3 μm thick) were cut (random starting section and orientation) with a distance between sections of 300 μm. Sections were stained with hematoxylin and eosin before dehydration in graded alcohols and mounting in DPX for morphometrical analysis. Estimation of the mean area of unilocular adipocytes was performed using an unbiased stereological technique which involved a Cavalieri grid overlay (grid size: 20 μm) [11]. Images were observed at x 20 magnification and 100 cells per section in 3 sections were chosen by systematic uniform sampling. Grid points falling onto the region of interest were counted (Stereo Investigator, MBF Bioscience, Williston, VT) and area estimates were calculated by multiplying the number of grid points counted by the area associated per grid point [12]. Results were adjusted for shrinkage during processing as determined by the measurement of 100 erythrocyte diameters and comparison with the standard diameter of erythrocytes in Wistar rats [13].

Measurement of mRNA expression by quantitative RT-PCR analysis

Total RNA was extracted from tissue samples using an RNeasy Lipid Tissue kit (Qiagen, Melbourne, Australia). RNA (1 μg) was reverse transcribed at 42°C for 120 min using murine Moloney Leukemia Virus Reverse Transcriptase (Promega, Madison, WI, USA) according to the manufacturer’s instructions and supplemented with 2.5 mg/mL Ficoll 400 and 7.5 mg/mL Ficoll 70 [14]. The resultant cDNA was purified using the UltraClean PCR Clean-up Kit (MoBio Laboratories Inc., Solana Beach, CA, USA). All primers, other than Il6, Il1b and Rpl19, were designed using Primer3 software [15], and were positioned to span introns to prevent amplification from contaminating genomic DNA; ribosomal Rpl19 was used as an internal control [16]. Quantitect primer sets for Il6 (QT00182896) and Il1b (QT00181657) were obtained from Qiagen (Melbourne, Australia) and amplified in Quantifast SYBR Green PCR mix according to the manufacturer’s instructions. For each of the remaining genes, the PCR primer sequences are shown in the Table 1 along with the presence or absence of 2.5 mg/mL Ficoll 400 and 7.5 mg/mL Ficoll 70 [14], MgCl2 concentrations, annealing temperatures, and PCR product sizes. External standards were generated from regular PCR products and ten-fold serial dilutions of the PCR product were made in RNase-free water (1- to 107 - fold dilutions). Quantitative PCR was performed in 10 μL reaction volumes using the Rotor-Gene 6000 system (Corbett Research, Sydney, Australia) with primer concentrations as specified in the Table 1, Immolase enzyme (0.5 U; Bioline, Alexandria, Australia), and 1/40 000 dilution of stock SYBR Green (Molecular Probes, Eugene, OR, USA) per reaction. The PCR cycling conditions included an initial denaturation at 94°C for 10 min followed by 45 cycles at 94°C for 1 s; an annealing temperature (specified in Table 1) for 15 s; and 72°C for 5 s. In each case, melt-curve analysis from 70 to 99°C showed a single PCR product that was confirmed to be the correct size and sequence by gel electrophoresis and sequence analysis respectively (data not shown). Fluorescence values were analyzed, standard curves constructed using the RotorGene software (Corbett Research, Sydney, Australia), and all samples standardized against a reference control (Rpl19).
Table 1

Primer sequences and conditions for quantitative PCR

Gene

Sequence

Cycling conditions (45 cycles)

Ficoll

MgCl 2 (mM)

Product size (bp)

11bHsd1

F: 5` ctctctgtgtcctcggcttc 3`

95°C/1 sec

No

2.5

131

 

R: 5` ttccatgatcctccttcctg 3`

57°C/15 sec

   
  

72°C/5 sec

   

Adiponectin

F: 5` tggcagagatggcactcc 3`

95°C/1 sec

No

4

101

 

R: 5` cttccgctcctgtcattcc 3`

59°C/15 sec

   
  

72°C/5 sec

   

GR

F: 5` cttgagaaacttacacctcgatgacc 3`

95°C/1 sec

Yes

4.5

461

 

R: 5` agcagtaggtaaggagattctcaacc 3`

62°C/20 sec

   
  

72°C/30 sec

   

Il1b

QT00182896

95°C/1 sec

No

-

-

  

60°C/30 sec

   

Il6

QT00181657

95°C/1 sec

No

-

-

  

60°C/30 sec

   

Pgc1a

F: 5` tctggaactgcaggcctaactc 3`

95°C/1 sec

No

4

96

 

R: 5` gcaagagggcttcagctttg 3`

60°C/15 sec

   
  

72°C/5 sec

   

Ppara

F: 5` aatccacgaagcctacctga 3`

95°C/1 sec

Yes

2.5

132

 

R: 5` gtcttctcagccatgcacaa 3`

60°C/15 sec

   
  

72°C/5 sec

   

Ppard

F: 5` gaggggtgcaagggcttctt 3`

95°C/1 sec

No

2.5

101

 

R: 5` cacttgttgcggttcttctg 3`

60°C/15 sec

   
  

72°C/5 sec

   

Pparg

F: 5` catgcttgtgaaggatgcaag 3`

95°C/1 sec

No

3

131

 

R: 5` ttctgaaaccgacagtactgacat 3`

63°C/15 sec

   
  

72°C/5 sec

   

Tnfa

F: 5` tactgaacttcggggtgattggtcc 3`

95°C/1 sec

No

2

295

 

R: 5` cagccttgtcccttgaagagaacc 3`

60°C/30 sec

   

Rpl19

F: 5`ctgaaggtcaaagggaatgtg 3`

95°C/1 sec

Yes

3

195

 

R: 5`ggacagagtcttgatgatctc 3`

52°C/15 sec

   
  

72°C/5 sec

   

Statistical analysis

All data are expressed as mean ± S.E.M., with each litter representing an ‘n’ of one. Analysis of variance (ANOVA) was used to attribute variation to sex, prenatal treatment, and postnatal diet. Where the F test was statistically significant (P < 0.05), specific differences were assessed by post hoc least significant difference (LSD) tests [17]. When a significant interaction term was observed, further analyses of data subsets were made by ANOVA or unpaired t tests as appropriate.

Results

Blood lipid profiles and adipocyte size

As previously reported male and female offspring of dexamethasone-treated mothers in this cohort were born smaller and had not shown catch-up growth by 6 months of age [4]. Male and female offspring that consumed the Std diet had comparable levels of serum triacylglycerols, cholesterol and HDL-C (Table 2). Postnatal consumption of the Hn3 diet lowered (P < 0.05) serum triacylglycerols (by 40-50% in males; 30-55% in females) and cholesterol (by 25-30% in males; 15-25% in females). Consumption of the Hn3 diet also reduced (by 20%; P = 0.02) adipocyte cross sectional area in male offspring irrespective of prenatal treatment (Figure 1B).
Table 2

Serum triacylglycerols, cholesterol and HDL-C in 6-month old offspring of control (Con) and dexamethasone (Dex)-treated mothers

 

Con/Std

Dex/Std

Con/Hn3

Dex/Hn3

Triaclyglycerols (mM)

    

Male

1.05 ± 0.23

0.75 ± 0.05

0.51 ± 0.03*

0.44 ± 0.04*

Female

0.89 ± 0.12

1.16 ± 0.16

0.62 ± 0.06*

0.53 ± 0.05*

Cholesterol (mM)

    

Male

2.53 ± 0.30

2.20 ± 0.11

1.94 ± 0.14*

1.53 ± 0.14*

Female

2.47 ± 0.16

2.05 ± 0.09

1.88 ± 0.07*

1.73 ± 0.19*

HDL-C (mM)

    

Male

1.93 ± 0.30

1.75 ± 0.11

1.57 ± 0.14

1.29 ± 0.14

Female

1.67 ± 0.16

1.34 ± 0.10

1.41 ± 0.07

1.39 ± 0.19

Offspring were raised on either a standard (Std) or a high omega-3 (Hn3) diet.

Values are the mean + SEM (n = 5–8 per group).

*P < 0.05 compared to corresponding Std diet (three-way ANOVA and LSD test).

Figure 1

Interactive effects of prenatal dexamethasone exposure and postnatal diet on adipose tissue cross-sectional area at 6 months of age in male rats. Histological images of retroperitoneal adipose tissue (A) and stereological quantitation of cross-sectional area of adipocytes (B). Control (Con) group in clear bars, Dex-exposed (Dex) group in black bars. Values are mean ± SEM (n = 5-8). Values without common notation differ significantly (P < 0.05; one-way ANOVA, LSD).

Serum fatty acid profile

Total fatty acid levels in serum were substantially elevated (81%; P < 0.01) in male (Table 3) but not female (data not shown) offspring of dexamethasone-treated mothers raised on the Std diet. In contrast, prenatal dexamethasone had minimal effect on serum fatty acid levels of offspring raised on the Hn3 diet (Table 2) with only C16:0, C18:0 and total fatty acid content increased. As expected, however, offspring raised on the Hn3 diet had elevated levels of all n-3 fatty acids, but lower levels of the n-6 fatty acids C20:4 and C22:4. Dietary effects in female offspring broadly paralleled those in males (results not shown).
Table 3

Serum concentrations of fatty acids (μg/mL) in male offspring at 6 months of age

 

Con/Std

Dex/Std

Con/Hn3

Dex/Hn3

C14:0

8 ± 1a

20 ± 2b

11 ± 1ac

16 ± 3bc

C16:0

155 ± 7a

289 ± 19b

165 ± 8a

215 ± 18c

C18:0

83 ± 9a

140 ± 9b

46 ± 5c

63 ± 9a

C16:1(n-7)

33 ± 4a

65 ± 9 b

53 ± 7 b

64 ± 3 b

C18:1 (n-9)

175 ± 15a

315 ± 28b

94 ± 8c

120 ± 11c

C18:2 (n-6)

53 ± 6a

125 ± 11b

58 ± 3a

79 ± 11a

C20:3 (n-6)

5 ± 1a

8 ± 1b

3 ± 0.5a

4 ± 0.5a

C20:4 (n-6)

225 ± 46a

372 ± 41b

63 ± 4c

73 ± 5c

C20:5 (n-3)

2 ± 0.5a

4.6 ± 0.4b

97 ± 9c

108 ± 14c

C22:4 (n-6)

3 ± 0.5a

9 ± 1a

0.5 ± 0.5b

0.5 ± 0.5b

C22:5 (n-3)

3 ± 0.5a

6 ± 1b

16 ± 1c

22 ± 3c

C22:6 (n-3)

25 ± 2a

46 ± 5b

66 ± 4c

83 ± 13c

Total n6

228 ± 46a

354 ± 48b

63 ± 4c

74 ± 5c

Total n3

30 ± 2a

54 ± 7b

179 ± 11c

213 ± 29c

Total

769 ± 65ac

1398 ± 86b

672 ± 27a

846 ± 94c

Data were analysed by two-way ANOVA followed by post hoc LSD tests.

Where there was an interaction between treatment and diet, separate t-tests were performed. For each fatty acid (i.e. within each row), values without common notation (a, b, c) differ significantly (P < 0.05).

Values are the mean ± SEM (n = 7 to 8 per group).

Programming of adipose cytokine expression

Adipose expression of both Il6 and Il1b mRNAs were upregulated by prenatal dexamethasone exposure (1.6-3-fold, P < 0.05) in male and female offspring raised on a Std diet, but these programmed increases were prevented in offspring raised on the Hn3 diet (Figure 2). Adipose expression of Tnfa mRNA was also elevated (2–3.5-fold, P < 0.001) in offspring of dexamethasone-treated mothers (Figure 2) regardless of postnatal diet. There was also a sex effect on adipose Tnfa expression (males < females; P = 0.006), and adipose expression of adiponectin was not affected by either prenatal dexamethasone or postnatal diet (data not shown).
Figure 2

Interactive effects of prenatal dexamethasone exposure and postnatal diet on Tnfa (A, D) Il6 (B, E) and Il1b (C, F) mRNA expression in adipose tissue in male (A-C) and female (D-F) rats. Control (Con) group in clear bars, Dex-exposed (Dex) group in black bars. Values are mean ± SEM (n = 5-8). Values without common notation differ significantly (P < 0.05; two-way ANOVA, LSD).

Glucocorticoid sensitivity of adipose tissue

Maternal dexamethasone treatment increased (P < 0.05) adipose GR mRNA expression irrespective of diet in both male and female offspring (Figure 3A & C). Adipose expression of 11bHsd1 was also upregulated (P < 0.05) in male but not female offspring of dexamethasone-treated mothers, particularly those raised on the Hn3 diet (Figure 3B & D).
Figure 3

Interactive effects of prenatal dexamethasone exposure and postnatal diet on GR (A, C) and 11bHsd1 (B, D) mRNAs in adipose tissue in male (A-B) and female (C-D) rats. Control (Con) group in clear bars; dexamethasone (Dex) group in black bars. Values are mean ± SEM (n = 5-8). Values without common notation differ significantly (P < 0.05; two-way ANOVA, LSD).

Adipose expression of PPARs

Maternal dexamethasone treatment increased adipose expression of Ppara (P = 0.008) in both male and female offspring regardless of diet (Figure 4). In contrast, Ppard expression was unaffected by prenatal dexamethasone but was upregulated (1.5-1.8-fold, P < 0.05) by consumption of the Hn3 diet at (Figure 4). Adipose expression of Pparg was unaffected by prenatal dexamethasone or postnatal diet in both males and females (results not shown). The PPAR co-activator, Pgc1a, was unaffected by prenatal treatment but was higher (P < 0.05) in male (but not female) offspring raised on the Hn3 diet (Figure 4C).
Figure 4

Interactive effects of prenatal dexamethasone exposure and postnatal diet on Ppara (A, D) Ppard (B, E) and Pgc1a (C, F) mRNA expression in adipose tissue in male (A-C) and female (D-F) rats. Control (Con) group in clear bars, Dex-exposed (Dex) group in black bars. Values are mean ± SEM (n = 5-8). Values without common notation differ significantly (P < 0.05; two-way ANOVA, LSD). *P < 0.05 compared to Std diet.

Discussion

Fetal glucocorticoid excess is recognised as a key mechanism involved in the programming of adverse phenotypic outcomes in adult offspring, including hypertension and insulin resistance. The present study showed that prenatal dexamethasone exposure programmed increased adipose inflammation and serum fatty acid levels at 6 months of age, and that consumption of a postnatal diet enriched with n-3 fatty acids alleviated many of these adverse outcomes. Specifically, adipose expression of Tnfa, Il6, Il1b, GR, 11bHsd1 and Ppara and serum fatty acid levels (males only) were all elevated in adult offspring of dexamethasone-treated mothers. Consumption of a diet enriched with n-3 fatty acids from birth corrected the programmed increases in serum fatty acids and adipose expression of Il6 and Il1b. Dietary supplementation with n-3 fatty acids also upregulated expression of Ppard and reduced mean adipocyte size regardless of prenatal treatment.

Disturbances to the normal fetal environment, such as excess glucocorticoid exposure or undernutrition, have been associated with a predisposition for adverse physiological outcomes in adult offspring including type II diabetes, hypertension and obesity in humans [18, 19] and rats [4, 5, 2022]. Our developmental programming model involves fetal glucocorticoid excess over the final third of rat pregnancy, which leads to fetal growth restriction [4, 7, 23] and subsequent development of offspring hypertension, hyperleptinemia [4], hyperinsulinemia and elevated plasma cytokine levels [5]. Although percent adiposity appeared unaffected in these programmed offspring [4], the present study shows that fetal glucocorticoid excess programmed marked changes in the adipose tissue phenotype. Most notably, adipose mRNA expression of the pro-inflammatory cytokines Tnfa, Il6 and Il1b was elevated in male and female offspring of dexamethasone-treated mothers, consistent with our previous report showing that plasma levels of these cytokines were elevated in this same cohort of animals [5]. Furthermore, although insulin sensitivity was not measured in these animals, analysis of fasting insulin levels indicated that prenatal dexamethasone treatment resulted in hyperinsulinemia [5]. This suggests that the pro-inflammatory state of adipose tissue may contribute to systemic inflammation and insulin resistance. Moreover, programming of the pro-inflammatory adipose phenotype was largely prevented when offspring were raised on the Hn3 diet, which normalised both Il6 and Il1b expression (but interestingly not that of Tnfa) and circulating insulin levels. This partial correction i.e. normalisation of Il6 and Il1b but not Tnfa, parallels the effects of the Hn3 diet on systemic inflammatory state [5] and the anti-inflammatory effects of the high n-3 diet are consistent with observations in a range of previous animal and human studies (for review see [24]). Exactly why programmed Tnfa expression is not corrected is unclear and requires further investigation.

A second key feature of the programmed adipose tissue phenotype was an apparent increase in glucocorticoid sensitivity, a characteristic linked to the aetiology of obesity [2527]. Thus, adipose expression of both the GR (Nr3c1) and 11bHsd1 mRNAs were both increased in offspring of dexamethasone-treated mothers. Glucocorticoid activation of the GR is enhanced by local expression of 11βHSD1, which catalyses regeneration of active corticosterone from inert 11-dehydrocorticosterone [28]. As such, these changes, coupled with increased stress-responsiveness of programmed offspring in this model [29], are likely to promote GR activation in adipose tissue. These observations extend those of Gnanalingham et al. (2005), who showed that prenatal dexamethasone exposure in a sheep model increased GR and 11βHSD1 levels in perirenal adipose tissue of newborns [30]. Our data are also consistent with the programmed upregulation of GR expression in kidney [31] and liver [32] following prenatal dexamethasone, and in adipose tissue after maternal undernutrition [22]. Collectively, these studies show that adipose glucocorticoid sensitivity is enhanced by fetal insults (nutritional or excess glucocorticoids).

This outcome might be expected to reduce adipose inflammation, given that glucocorticoids are normally potent anti-inflammatory agents. Indeed, glucocorticoids and pro-inflammatory cytokines are thought to act synergistically to stimulate 11bHsd1 expression in acute inflammation, thereby further enhancing local levels of active glucocorticoid to perhaps limit inflammation (for review see [6]). But if this acute inflammation is not resolved and chronic inflammation ensues, as in metabolic disease, the anti-inflammatory action of glucocorticoids appears to be lost [6]. Interestingly, a similar scenario is evident in the late gestation rat placenta, where increased expression of pro-inflammatory cytokines [33], GR and 11bHsd1[23] all occur despite rising levels of maternal and fetal glucocorticoids.

The PPAR transcription factors play key roles in adipocyte differentiation and function, influencing the balance between fat storage (via PPARγ) and utilisation (via PPARδ) (for reviews see [34, 35]). Although prenatal dexamethasone did not affect adipose expression of either Pparg or Ppard, it did program a marginal increase in adipose expression of Ppara, particularly in female offspring. This effect may have developed as a compensatory response to the heightened adipose inflammatory state, since PPARα activation is known to exert anti-inflammatory effects in other cell types [36]. Interestingly, these Ppard responses to diet are different to those observed in the skeletal muscle of the same rats [5], where elevated Ppard expression was programmed by prenatal Dex exposure, but was unaffected by diet. This likely represents tissue-specific regulation of Ppard.

Male offspring of dexamethasone-treated mothers showed elevated serum levels of total fatty acids, an effect evident across all fatty acid groups. While the specific reasons why this effect was limited to male offspring are not known, gender differences have been noted in fatty acid oxidation rates in humans (females lower than males; for review see [37]). Although previous studies have reported a programmed increase in serum free fatty acid and triacylglycerol levels (by maternal obesity; [38]), importantly this was observed in offspring that were themselves obese. In contrast, the programmed increase in serum fatty acids in the present study occurred in the absence of increased adiposity, possibly indicative of a greater susceptibility to obesogenic stimuli. It is possible that the programming of elevated serum fatty acids by dexamethasone may be linked, in part, to the elevated levels of pro-inflammatory cytokines [5], since these cytokines are known to increase lipolysis in both humans and rats [39, 40]. In this context it is noteworthy that adipose expression of Il6 was also corrected by the Hn3 diet.

Consumption of the Hn3 diet markedly reduced serum levels of triacylglycerols and cholesterol, but did not affect HDL-C levels, consistent with known effects of n-3 fatty acids on lipid profiles in humans [41]. This dietary effect may reflect inhibition of hepatic triacylglycerol synthesis and stimulation of beta-oxidation by n-3 fatty acids [42], effects that are likely to have contributed to the decreased adipocyte size in rats fed the Hn3 diet. Elevated expression of Ppard was also observed in these smaller adipocytes, consistent with previous studies in rats that consumed n-3 fatty acids [43]. Activation of PPARδ in adipocytes leads to improved lipid profiles and reduced adiposity [44] and n-3 fatty acids are known ligands for PPARs [45]. Decreased adipocyte size has also been associated with increased insulin sensitivity, a reduced incidence of type II diabetes in rats [46] and humans [47] as well as reduced expression and release of adipocytokines [48, 49], suggestive of a less detrimental phenotype associated with the smaller adipocytes. Furthermore, this reduced adipocyte size is consistent with the observed decline in epididymal fat pad weight previously reported for these animals [4].

Conclusions

This study demonstrates that prenatal dexamethasone exposure programmed detrimental changes in the adipocyte phenotype including a pro-inflammatory state and increased glucocorticoid sensitivity. Consumption of a postnatal diet enriched with n-3 fatty acids attenuated pro-inflammatory adipocytokine responses, decreased adipose cross-sectional area and alleviated many of these adverse programming effects of fetal glucocorticoid excess.

Abbreviations

11βHSD /11bHsd: 

11β hydroxysteroid dehydrogenase

ANOVA: 

Analysis of variance

GR: 

Glucocorticoid receptor

HDL: 

High density lipoprotein

Hn3: 

High omega3

IL: 

Interleukin

LSD: 

Least significant difference

MgCl2: 

Magnesium chloride

PGC1α/Pgc1a: 

PPAR gamma co-activator 1 alpha

PPAR/Ppar: 

Peroxisome proliferator activated receptor

RNA: 

Ribonucleic acid

RNase-free: 

Ribonuclease-free

RT-PCR: 

Reverse transcription polymerase chain reaction

Std: 

Standard

TNFα/Tnfa: 

Tumour necrosis factor alpha.

Declarations

Acknowledgements

Supported by National Health and Medical Research Council Project Grant. The authors wish to thank Jessica Lewis and Maike Bollen (School of Anatomy, Physiology & Human Biology, The University of Western Australia) for their technical assistance during the data collection.

Authors’ Affiliations

(1)
School of Anatomy, Physiology & Human Biology, The University of Western Australia
(2)
School of Medicine and Pharmacology, The University of Western Australia

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© Mark et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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