Intrauterine Exposure to High Saturated Fat Diet Elevates Risk of Adult-onset Chronic Diseases in C57BL/6 Mice
Overview
Authors
Affiliations
Background: The developmental environment is thought to determine, in part, lifelong metabolic parameters and risk of adult disease. Effects of maternal malnutrition on fetal growth have been studied extensively, and the role of poor prenatal diet in elevating lifelong risk of cardiovascular and metabolic disease has been well characterized (www.thebarkertheory.com). However, the contribution of gestational high saturated fat diet (HFD) to adult-onset metabolic disease and skeletal dysfunction has only recently been recognized, and as such is incompletely understood.
Methods: The present study evaluates the pathophysiologic mechanisms linking gestational HFD (approximating the macronutrient content of fast food) and elevated oxidative stress (OS) to adult-onset skeletal, cardiovascular, and metabolic dysfunction.
Results: Results of this study demonstrate that adult offspring of dams fed HFD during pregnancy exhibited adult hyperglycemia, insulin resistance, obesity, and hypertension, despite being fed healthy standard rodent chow throughout postnatal life. These offspring also showed significantly lower femoral epiphyseal average bone mineral density (ABMD) at 6 months of age, and dysregulation of distal femoral trabecular architecture at 12 months of age, characteristic of osteoporosis. Incidence of these adult-onset adverse skeletal and metabolic effects was reduced by supplementing the pregnant dam with the antioxidant (quercetin, Q) during pregnancy.
Conclusions: Collectively, these data suggest that offspring of dams who consume a diet rich in saturated fats during pregnancy are at increased risk of adult-onset chronic disease. Additionally, these chronic diseases were determined to be in-part OS-mediated, and preventable by increasing a prenatal dietary antioxidant; this knowledge offers both a putative mechanism of disease pathogenesis and suggests a potential preventive strategy.
Kidney Programming and Hypertension: Linking Prenatal Development to Adulthood.
Tain Y, Hsu C Int J Mol Sci. 2025; 25(24.
PMID: 39769369 PMC: 11677590. DOI: 10.3390/ijms252413610.
Pregnancy in obese women and mechanisms of increased cardiovascular risk in offspring.
Cochrane A, Murphy M, Ozanne S, Giussani D Eur Heart J. 2024; 45(48):5127-5145.
PMID: 39508438 PMC: 11663486. DOI: 10.1093/eurheartj/ehae671.
Maternal Polyphenols and Offspring Cardiovascular-Kidney-Metabolic Health.
Tain Y, Hsu C Nutrients. 2024; 16(18).
PMID: 39339768 PMC: 11434705. DOI: 10.3390/nu16183168.
Tain Y, Hsu C Int J Mol Sci. 2024; 25(18).
PMID: 39337276 PMC: 11432268. DOI: 10.3390/ijms25189788.
Xhonneux I, Marei W, Meulders B, Slootmans J, Pintelon I, Leroy J PLoS One. 2024; 19(6):e0305912.
PMID: 38935642 PMC: 11210809. DOI: 10.1371/journal.pone.0305912.