Cited by 54Birth, Development, and HealthGenetic Syndromes and ImprintingDiet, Metabolism, and Disease

Prenatal Low-Protein and Postnatal High-Fat Diets Induce Rapid Adipose Tissue Growth by Inducing Igf2 Expression in Sprague Dawley Rat Offspring

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Claycombe, Kate J., Uthus, Eric O., Roemmich, James N., Johnson, LuAnn K., Johnson, W. Thomas·2013·The Journal of Nutrition

Abstract

Maternal low-protein diets result in lower birth weight followed by accelerated catch-up growth that is accompanied by the development of obesity and glucose intolerance in later life. Whether postnatal high-fat (HF) diets further contribute to the development of obesity and insulin resistance in offspring by affecting adipose tissue metabolism and DNA methylation is currently unknown. Obese-prone Sprague-Dawley rats were fed 8% low protein (LP) or 20% normal protein diets for 3 wk prior to conception and throughout pregnancy and lactation to investigate whether prenatal LP and postnatal HF diets affect the rate of adipose tissue growth, insulin-like growth factor 2 (Igf2) expression, and DNA methylation in male offspring. At weaning, the offspring were fed 10% normal fat or 45% HF diets for 12 wk. The adipose tissue growth rate was increased (up to 26-fold) by the LP prenatal and HF postnatal diets. Adipose tissue Igf2 mRNAs and DNA methylation were increased by the LP prenatal and HF postnatal diets. The LP prenatal and HF postnatal diet increased the number of small adipocytes in adipose tissue and decreased insulin sensitivity. These findings suggest that prenatal LP and postnatal HF intake result in adipose tissue catch-up growth through alterations in the expression of the Igf2 gene and DNA methylation within adipocytes. These alterations in adiposity are accompanied by an increased risk of development of type 2 diabetes.

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Crossref · 10.3945/jn.113.178038

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  • There are changes in leptin, adiponectin, and other important hormones like IGFs in the adipose of offspring from low protein diet-fed mothers, which may contribute to their enhanced adiposity postnatally.

    “Importantly there are changes in leptin, adiponectin, and other important hormones like IGFs in the adipose of offspring [81, 83], which may contribute to their enhanced adiposity postnatally.”

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Authors
Claycombe, K. J., Uthus, E. O., Roemmich, J. N., Johnson, L. K., & Johnson, W. T.
Affiliations
Agricultural Research Service (US)
Corresponding author
Claycombe, Kate J.
Venue
The Journal of Nutrition
Publisher
Elsevier BV
Published
2013-10
Volume
143
Issue
10
Pages
1533-1539
ISSN
0022-3166 (ISSN-L)
OpenAlex
W2164770758
Cited by
54
References
1
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2022: 1 · 2021: 5 · 2020: 4 · 2019: 3 · 2018: 6 · 2017: 11 · 2016: 8 · 2015: 3 · 2014: 6 · 2013: 1
FWCI
5.59
Type
journal article
Language
en
Open access
Locations
  • Journal of Nutrition (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Agriculture
  • Agricultural Research Service (5450‐51000‐047‐00D)
Topics
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
Keywords
maternal low-protein diet, adipose tissue expansion, IGF2 expression, DNA methylation, catch-up growth, obesity, insulin resistance, type 2 diabetes, adipocyte size, Sprague-Dawley rats, prenatal programming, offspring adiposity
MeSH terms
Adipose Tissue, Animals, Dietary Fats, Dietary Proteins, Female, Insulin Resistance, Insulin-Like Growth Factor II, Lactation, Obesity, Pregnancy, Prenatal Exposure Delayed Effects, RNA, Messenger, Weaning, Rats, Sprague-Dawley, Adipocytes, Diet, Protein-Restricted, DNA Methylation, Prenatal Nutritional Physiological Phenomena, Rats, Diet, High-Fat

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