Cited by 240Birth, Development, and HealthRegulation of Appetite and ObesityReproductive Physiology in Livestock

Maternal Endocrine Adaptation throughout Pregnancy to Nutritional Manipulation: Consequences for Maternal Plasma Leptin and Cortisol and the Programming of Fetal Adipose Tissue Development

Bispham, J., Gopalakrishnan, G. S., Dandrea, J., Wilson, V., Budge, H., Keisler, D. H., Broughton Pipkin, F., Stephenson, T. +1 more·2003·Endocrinology

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 adult disease. We investigated the effect of gestational age and maternal nutrition on the maternal plasma concentration of leptin and cortisol together with effects on fetal adipose tissue deposition plus leptin, IGF-I, IGF-II ligand, and receptor mRNA abundance near to term. Singleton bearing ewes were either nutrient restricted (NR; consuming 3.2-3.8 MJ/d of metabolizable energy) or fed to appetite (consuming 8.7-9.9 MJ/d) 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, consuming 6.7-7.5 MJ/d, or were fed to appetite and consumed 8.0-10.9 MJ/d. Pregnancy resulted in a rise in plasma leptin concentration by 28 d gestation, which continued up to 80 d gestation when fed to appetite but not with nutrient restriction. Plasma cortisol was also lower in NR ewes up to 80 d gestation, a difference no longer apparent when food intake was increased. At term, irrespective of maternal nutrition in late gestation, fetuses sampled from ewes NR in early gestation possessed more adipose tissue, whereas when ewes were fed to appetite throughout gestation, fetal adipose tissue deposition and leptin mRNA abundance were both reduced. These changes may result in the offspring of NR mothers being at increased risk of obesity in later life.

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Crossref · 10.1210/en.2003-0320

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  • Restoring maternal diets to the same as controls after day 80 of gestation further stimulated fat deposition in the fetus.

    “Bisham et al. [66] found that restoring maternal diets to the same as controls after day 80 of gestation further stimulated fat deposition in the fetus.”

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References 49 · Cited by 240

Authors
Bispham, J., Gopalakrishnan, G. S., Dandrea, J., Wilson, V., Budge, H., Keisler, D. H., Broughton Pipkin, F., Stephenson, T., & Symonds, M. E.
Affiliations
  • University of Nottingham (GB)
  • University of Missouri (US)
Corresponding author
Symonds, M. E.
Venue
Endocrinology
Published
2003-08
Volume
144
Issue
8
Pages
3575-3585
ISSN
  • 0013-7227 (ISSN-L)
  • 1945-7170
OpenAlex
W2029380451
Cited by
240
References
49
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 6 · 2022: 3 · 2021: 8 · 2020: 8 · 2019: 3 · 2018: 6 · 2017: 11 · 2016: 8 · 2015: 14 · 2014: 13 · 2013: 7 · 2012: 15
FWCI
16.75
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 › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
  • Life Sciences › Agricultural and Biological Sciences › Agronomy and Crop Science › Reproductive Physiology in Livestock
Keywords
maternal nutrient restriction, fetal programming, leptin, cortisol, fetal adipose tissue, insulin-like growth factor I, insulin-like growth factor II, placental development, gestational age, maternal energy intake, ewes, obesity risk
MeSH terms
Adaptation, Physiological, Adipose Tissue, Animals, Body Composition, Body Weight, Energy Intake, Eating, Female, Food Deprivation, Gestational Age, Hydrocortisone, Insulin-Like Growth Factor I, Insulin-Like Growth Factor II, Nutritional Physiological Phenomena, Organ Size, Placenta, Pregnancy, Pregnancy, Animal, Prolactin, RNA, Messenger, Sheep, Thyroxine, Receptor, IGF Type 2, Leptin

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