Paternal high protein diet modulates body composition, insulin sensitivity, epigenetics, and gut microbiota intergenerationally in rats

FASEB J. 2021 Sep;35(9):e21847. doi: 10.1096/fj.202100198RR.

Abstract

Mounting evidence demonstrates that paternal diet programs offspring metabolism. However, the contribution of a pre-conception paternal high protein (HP) diet to offspring metabolism, gut microbiota, and epigenetic changes remains unclear. Here we show that paternal HP intake in Sprague Dawley rats programs protective metabolic outcomes in offspring. Compared to paternal high fat/sucrose (HF/S), HP diet improved body composition and insulin sensitivity and improved circulating satiety hormones and cecal short-chain fatty acids compared to HF/S and control diet (P < .05). Further, using 16S rRNA gene sequencing to assess gut microbial composition, we observed increased alpha diversity, distinct bacterial clustering, and increased abundance of Bifidobacterium, Akkermansia, Bacteroides, and Marvinbryantia in HP fathers and/or male and female adult offspring. At the epigenetic level, DNMT1and 3b expression was altered intergenerationally. Our study identifies paternal HP diet as a modulator of gut microbial composition, epigenetic markers, and metabolic function intergenerationally.

Keywords: 16S rRNA sequencing; DNA methyltransferase; body composition; epigenetics; gut microbiota; high protein diet; insulin sensitivity; paternal nutrition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Adiposity
  • Aging
  • Animals
  • Body Composition*
  • Body Weight
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • Diet, High-Fat
  • Diet, High-Protein*
  • Dietary Sucrose
  • Energy Intake
  • Energy Metabolism
  • Epigenesis, Genetic*
  • Fathers*
  • Fatty Acids / metabolism
  • Female
  • Fertility
  • Gastrointestinal Microbiome*
  • Glucose Tolerance Test
  • Hormones / metabolism
  • Insulin / metabolism*
  • Insulin Resistance
  • Liver / metabolism
  • Male
  • Organ Size
  • Paternal Exposure*
  • Pregnancy
  • RNA, Small Untranslated / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Satiety Response
  • Weaning

Substances

  • Dietary Sucrose
  • Fatty Acids
  • Hormones
  • Insulin
  • RNA, Small Untranslated
  • DNA (Cytosine-5-)-Methyltransferases