Paternal High-Protein Diet Programs Offspring Insulin Sensitivity in a Sex-Specific Manner.
Pengfei GongDanielle BailbéLola BianchiGaëlle PommierJunjun LiuStefania ToluMaria G StathopoulouBernard PorthaValerie GrandjeanJamileh MovassatPublished in: Biomolecules (2021)
The impact of maternal nutrition on offspring is well documented. However, the implication of pre-conceptional paternal nutrition on the metabolic health of the progeny remains underexplored. Here, we investigated the impact of paternal high-protein diet (HPD, 43.2% protein) consumption on the endocrine pancreas and the metabolic phenotype of offspring. Male Wistar rats were given HPD or standard diet (SD, 18.9% protein) for two months. The progenies (F1) were studied at fetal stage and in adulthood. Body weight, glycemia, glucose tolerance (GT), glucose-induced insulin secretion in vivo (GIIS) and whole-body insulin sensitivity were assessed in male and female F1 offspring. Insulin sensitivity, GT and GIIS were similar between F1 females from HPD (HPD/F1) and SD fathers (SD/F1). Conversely, male HPD/F1 exhibited increased insulin sensitivity (p < 0.05) and decreased GIIS (p < 0.05) compared to male SD/F1. The improvement of insulin sensitivity in HPD/F1 was sustained even after 2 months of high-fat feeding. In male HPD/F1, the β cell mass was preserved and the β cell plasticity, following metabolic challenge, was enhanced compared to SD/F1. In conclusion, we provide the first evidence of a sex-specific impact of paternal HPD on the insulin sensitivity and GIIS of their descendants, demonstrating that changes in paternal nutrition alter the metabolic status of their progeny in adulthood.
Keyphrases
- physical activity
- high fat diet
- body weight
- protein protein
- weight loss
- amino acid
- binding protein
- depressive symptoms
- healthcare
- cell therapy
- risk assessment
- body mass index
- stem cells
- mental health
- adipose tissue
- blood pressure
- social media
- pregnant women
- early life
- metabolic syndrome
- mesenchymal stem cells
- endothelial cells
- blood glucose
- small molecule
- human health
- diabetic rats
- single molecule
- atomic force microscopy