Maternal Nutritional Programming of Fetal Adipose Tissue Development: Differential Effects on Messenger Ribonucleic Acid Abundance for Uncoupling Proteins and Peroxisome Proliferator-Activated and Prolactin Receptors
Abstract
Maternal nutrient restriction at specific stages of gestation has differential effects on fetal development such that the offspring are programmed to be at increased risk of a range of adult diseases, including obesity. We investigated the effect of maternal nutritional manipulation through gestation on fetal adipose tissue deposition in conjunction with mRNA abundance for uncoupling protein (UCP)1 and 2, peroxisome proliferator-activated receptors (PPAR)alpha and gamma, together with long and short forms of the prolactin receptor (PRLR). Singleton-bearing ewes were either nutrient restricted (3.2-3.8 MJ day(-1) metabolizable energy) or fed to appetite (8.7-9.9 MJ day(-1)) over the period of maximal placental growth, i.e. between 28 and 80 d gestation. After 80 d gestation, ewes were either fed to calculated requirements, (6.7-7.5 MJ day(-1)), or to appetite (8.0-10.9 MJ day(-1)). At term, offspring of nutrient-restricted ewes possessed more adipose tissue, an adaptation that was greatest in those born to mothers that fed to requirements in late gestation. This was accompanied by an increased mRNA abundance for UCP2 and PPARalpha, an adaptation not seen in mothers re-fed to appetite. Maternal nutrition had no effect on mRNA abundance for UCP1, PPARgamma, or PRLR. Irrespective of maternal nutrition, mRNA abundance for UCP1 was positively correlated with PPARgamma and the long and short forms of PRLR, indicating that these factors may act together to ensure that UCP1 abundance is maximized in the newborn. In conclusion, we have shown, for the first time, differential effects of maternal nutrition on key regulatory components of fetal fat metabolism.
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Enhanced adiposity is accompanied by changes in PPAR and UCP1/2 abundance in the adipose of offspring from undernourished mothers, and the timing of maternal nutrient restriction determines the nature of the molecular changes and level of adiposity.
“Enhanced adiposity is also accompanied by changes in PPAR and UCP1/2 abundance in the adipose of offspring from undernourished mothers, however the timing of the maternal nutrient restriction seems to determine the nature of the molecular changes and level of adiposity [60, 63–65].”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [60]
Maternal nutrient and caloric restriction in a number of animal models programmes the offspring for increased adiposity.
“Maternal nutrient and caloric restriction in a number of animal models has also been found to programme the offspring for increased adiposity ([60, 61] and Table 1).”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [60]
Maternal nutrient restriction is often accompanied by decreased fetal growth or birth weight of the offspring.
“Maternal nutrient restriction is often accompanied by decreased fetal growth or birth weight of the offspring [60, 62, 63, 65].”
From Developmental programming of offspring adipose tissue biology and obesity risk (2021) · cites this paper as [60]
Cites
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Developmental programming of obesity in mammals
Taylor, P. D., & Poston, L. (2007) · Experimental Physiology · doi:10.1113/expphysiol.2005.032854 · Cited by 473 · see citing works
Fetal origins of the metabolic syndrome
Xita, N., & Tsatsoulis, A. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05658.x · Cited by 96 · see citing works
Developmental programming of offspring adipose tissue biology and obesity risk
Rodgers, A., & Sferruzzi-Perri, A. N. (2021) · International Journal of Obesity · doi:10.1038/s41366-021-00790-w · Cited by 57 · see citing works
Correia-Branco, A., Keating, E., & Martel, F. (2015) · Reproductive Sciences · doi:10.1177/1933719114542012 · Cited by 55 · see citing works
- Authors
- Bispham, J., Gardner, D. S., Gnanalingham, M. G., Stephenson, T., Symonds, M. E., & Budge, H.
- Affiliations
- University of Nottingham (GB)
- Corresponding author
- Symonds, M. E.
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 2005-09-01
- Volume
- 146
- Issue
- 9
- Pages
- 3943-3949
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2075899993
- Cited by
- 101
- References
- 2
- Citations by year
- 2024: 1 · 2023: 4 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 5 · 2017: 2 · 2016: 8 · 2015: 6 · 2014: 3 · 2013: 6 · 2012: 12
- FWCI
- 6.08
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Life Sciences › Agricultural and Biological Sciences › Agronomy and Crop Science › Reproductive Physiology in Livestock
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- fetal adipose tissue, maternal nutrient restriction, UCP1, UCP2, PPARα, PPARγ, prolactin receptor, mRNA levels, obesity risk, ewes, placental development
- MeSH terms
- Uncoupling Protein 2, Uncoupling Protein 1, Adipose Tissue, Animals, Carrier Proteins, Female, Fetus, Ion Channels, Membrane Proteins, Receptors, Prolactin, RNA, Messenger, Sheep, Mitochondrial Proteins, Membrane Transport Proteins, PPAR alpha, PPAR gamma, Fetal Nutrition Disorders
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