Abstract
Maternal high-fat or high-salt diets can independently program adverse cardiometabolic outcomes in offspring. However, there is a paucity of evidence examining their effects in combination on metabolic function in adult offspring. Female Sprague Dawley rats were randomly assigned to either: control (CD; 10% kcal from fat, 1% NaCl), high-salt (SD; 10% kcal from fat, 4% NaCl), high-fat (HF; 45% kcal from fat, 1% NaCl) or high-fat and salt (HFSD; 45% kcal from fat, 4% NaCl) diets 21 days prior to mating and throughout pregnancy and lactation. Male offspring were weaned onto a standard chow diet and were culled on postnatal day 130 for plasma and tissue collection. Adipocyte histology and adipose tissue, liver, and gut gene expression were examined in adult male offspring. HF offspring had significantly greater body weight, impaired insulin sensitivity and hyperleptinemia compared to CD offspring, but these increases were blunted in HFSD offspring. HF offspring had moderate adipocyte hypertrophy and increased expression of the pre-adipocyte marker Dlk1. There was a significant effect of maternal salt with increased hepatic expression of Dgat1 and Igfb2. Gut expression of inflammatory (Il1r1, Tnfα, Il6, and Il6r) and renin–angiotensin system (Agtr1a, Agtr1b) markers was significantly reduced in HFSD offspring compared to HF offspring. Therefore, salt mitigates some adverse offspring outcomes associated with a maternal HF diet, which may be mediated by altered adipose tissue morphology and gut inflammatory and renin–angiotensin regulation.
Highlights
The incidence of obesity and related non-communicable diseases, including type 2 diabetes, cardiovascular diseases, and some cancers continues to rise
A Maternal high fat (HF) Diet Programmed an Adverse Metabolic Phenotype in Adult Male Offspring, Which Was Not Exacerbated by the Addition of Salt to the Maternal Diet
We found that a maternal purified high-fat and high-salt diet group (HFSD) diet resulted in significantly reduced weight, increased insulin sensitivity, and reduced circulating leptin concentrations in offspring compared to those exposed to a maternal HF diet alone
Summary
The incidence of obesity and related non-communicable diseases, including type 2 diabetes, cardiovascular diseases, and some cancers continues to rise These conditions have a genetic component, the rapid rate at which these conditions have increased underscores the influence of a rapidly changing lifestyle. Weidemann et al have shown in mice that dietary sodium prevented weight gain in HF feeding, despite no difference in food intake or metabolic rate [8]. This was suggested to be due to reduced digestive efficiency by suppression of the renin–angiotensin system (RAS). The reported effects of diets high in both fat and salt are conflicting
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.