Abstract

Experimental and epidemiological evidence demonstrate that ancestral diet might contribute towards offspring health. This suggests that nutrition may be able to modify genetic or epigenetic information carried by germ cells (GCs). To examine if a parental high fat diet (HFD) influences metabolic health in two generations of offspring, GC-eGFP Sprague Dawley rats were weaned onto HFD (45% fat) or Control Diet (CD; 10% fat). At 19 weeks, founders (F0) were bred with controls, establishing the F1 generation. HFD resulted in 9.7% and 14.7% increased weight gain in male and female F0 respectively. F1 offspring of HFD mothers and F1 daughters of HFD-fed fathers had increased weight gain compared to controls. F1 rats were bred with controls at 19 weeks to generate F2 offspring. F2 male offspring derived from HFD-fed maternal grandfathers exhibited increased adiposity, plasma leptin and luteinising hormone to testosterone ratio. Despite transmission via the founding male germline, we did not find significant changes in the F0 intra-testicular GC transcriptome. Thus, HFD consumption by maternal grandfathers results in a disrupted metabolic and reproductive hormone phenotype in grandsons in the absence of detectable changes in the intra-testicular GC transcriptome.

Highlights

  • Cardiovascular Science, University of Edinburgh, QMRI, 47 Little France Crescent, EH16 4TJ, UK. *These authors contributed to this work

  • From weaning male and female rats were placed onto a control diet (CD) or onto a high fat diet (HFD) for 16 weeks

  • The aim of the present studies was to investigate if feeding rats a HFD results in metabolic or reproductive changes in subsequent generations and, if so, whether this might be mediated via altered gene expression in the GCs of the HFD-exposed parents

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Summary

Introduction

Cardiovascular Science, University of Edinburgh, QMRI, 47 Little France Crescent, EH16 4TJ, UK. *These authors contributed to this work. No differences were observed in litter size, percentage of males per litter or birth-weights of F2 grand-offspring of CD or HFD fed rats (Supplementary Table 2).

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