Abstract

The need to refine rodent models of human-related disease is now being recognized, in particular the rearing environment that can profoundly modulate metabolic regulation. Most studies on pregnancy and fetal development purchase and transport young females into the research facility, which after a short period of acclimation are investigated (Gen0). We demonstrate that female offspring (Gen1) show an exaggerated hyperinsulinemic response to pregnancy when fed a standard diet and with high fructose intake, which continues throughout pregnancy. Markers of maternal hepatic metabolism were differentially influenced, as the gene expression of acetyl-CoA-carboxylase was raised in Gen1 given fructose and controls, whereas glucose transporter 5 and fatty acid synthase expression were only raised with fructose. Gen1 rats weighed more than Gen0 throughout the study, although fructose feeding raised the percent body fat but not body weight. We show that long-term habituation to the living environment has a profound impact on the animal’s metabolic responses to nutritional intervention and pregnancy. This has important implications for interpreting many studies investigating the influence of maternal consumption of fructose on pregnancy outcomes and offspring to date.

Highlights

  • Diabetes and metabolic syndrome are normally considered to result from exposure to an obesogenic environment together with an individual’s genotype [1]

  • Gen1 that is exacerbated by a high intake of fructose and was corroborated by the fact that the insulin

  • We suggest that the negative impact of nutritional programming on offspring glucose and lipid homeostasis mediated by fructose feeding [11,12,32] has been significantly underestimated

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Summary

Introduction

Diabetes and metabolic syndrome are normally considered to result from exposure to an obesogenic environment together with an individual’s genotype [1]. It is recognized that in populations that migrate to more affluent countries, it is the generation that is at greater risk of becoming diabetic, in part due to early life exposures [2,3]. These factors are seldom considered in animal models of diabetes, especially those examining the impact of exposure to an adverse maternal nutritional environment on the offspring. Nutrients 2017, 9, 327 that fructose in pregnancy can significantly reduce the weight of the placenta [11], and increase the expression of genes related to lipogenesis in the offspring liver [12].

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