Abstract

To begin to understand the contributions of maternal obesity and over-nutrition to human development and the early origins of obesity, we utilized a non-human primate model to investigate the effects of maternal high-fat feeding and obesity on breast milk, maternal and fetal plasma fatty acid composition and fetal hepatic development. While the high-fat diet (HFD) contained equivalent levels of n-3 fatty acids (FA's) and higher levels of n-6 FA's than the control diet (CTR), we found significant decreases in docosahexaenoic acid (DHA) and total n-3 FA's in HFD maternal and fetal plasma. Furthermore, the HFD fetal plasma n-6∶n-3 ratio was elevated and was significantly correlated to the maternal plasma n-6∶n-3 ratio and maternal hyperinsulinemia. Hepatic apoptosis was also increased in the HFD fetal liver. Switching HFD females to a CTR diet during a subsequent pregnancy normalized fetal DHA, n-3 FA's and fetal hepatic apoptosis to CTR levels. Breast milk from HFD dams contained lower levels of eicosopentanoic acid (EPA) and DHA and lower levels of total protein than CTR breast milk. This study links chronic maternal consumption of a HFD with fetal hepatic apoptosis and suggests that a potentially pathological maternal fatty acid milieu is replicated in the developing fetal circulation in the nonhuman primate.

Highlights

  • Over the last twenty years, obesity has dramatically increased in the United States across every ethnic group studied [1,2]

  • Maternal diet nutritional analysis To initiate our analysis of the impact that maternal high-fat diet (HFD) has on the developing nonhuman primates (NHP) fetus, we chose to first examine differences in fatty acid composition between the control diet (CTR) and HFD diets

  • Using gas chromatography-mass spectroscopy, we found that compared to the CTR diet, the maternal HFD has higher levels of myristic (C14:0), myristoleic (C14:1), palmitic (C16:0), palmitoleic (C16:1), stearic (C18:0), oleic (C18:1, n-9), linoleic (LA, C18:2, n-6), alinolenic (ALA, C18:3, n-3), and arachidonic (AA, C20:4, n-6) fatty acids

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Summary

Introduction

Over the last twenty years, obesity has dramatically increased in the United States across every ethnic group studied [1,2]. A concerning part of the emerging epidemic of obesity is the increasing rise in the percentage of children and adolescents that are either overweight or at risk for overweight [1,2,5]. The increasing prevalence of metabolic diseases and obesity in children is most often attributed to a combination of an energy conserving, or ‘thrifty’ genotype, with a prevalent imbalance of nutrient intake and expenditure in the developed world. An emerging body of evidence suggests that our ability to respond to metabolic challenges during postnatal life is modified by environmental influences during fetal development. Fetal development is a critical period when exposure to environmental insults in-utero has lifelong effects on the structure and function of organs, tissues and body systems in the offspring

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