Frequent and mild scrotal heat stress in mice epigenetically alters glucose metabolism in the male offspring

Am J Physiol Endocrinol Metab. 2020 Aug 1;319(2):E291-E304. doi: 10.1152/ajpendo.00038.2020. Epub 2020 Jun 30.

Abstract

Several studies have reported that health problems occur in assisted reproductive technology (ART)-conceived offspring. Recently, investigations have demonstrated that paternal environmental conditions influence offspring health. However, it is unclear whether the factors that cause male infertility per se affect offspring health and contribute to health problems in ART-born children. Scrotal heat stress represents a common cause for oligoasthenozoospermia, and in these cases, in vitro fertilization-embryo transfer (IVF-ET) is typically recommended for those individuals trying to conceive. We exposed C57BL/6J male mice to frequent and mild scrotal heat stress (fmSHS) (39°C for 30 min once weekly for 5 consecutive wk). Sperm was subjected to IVF-ET with oocytes of untreated C57BL/6J females to produce offspring mice. Glucose intolerance and insulin resistance was observed in the male offspring mice derived from fmSHS-exposed fathers. Islets, after evaluation, remained unchanged. Genes involved in glucose metabolism, especially, those in insulin signaling pathways, showed dysregulation in the liver of the fmSHS-derived male offspring. Differentially methylated regions were found in the sperm of fmSHS-exposed mice by whole genome bisulfite sequencing. Interestingly, abnormal methylation of some genes with altered expression in offspring was observed in both the sperm of fmSHS fathers and the liver of their male offspring. Our results suggest that the factors that cause male infertility can affect male offspring health by an epigenetic mechanism.

Keywords: assisted reproductive technology; epigenetics; glucose metabolism; male infertility; offspring health.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA Methylation
  • Embryo Transfer
  • Epigenesis, Genetic / physiology*
  • Female
  • Fertilization in Vitro
  • Glucose / metabolism*
  • Glucose Intolerance / etiology
  • Glucose Intolerance / pathology
  • Hot Temperature*
  • Infertility, Male / etiology
  • Infertility, Male / genetics*
  • Insulin Resistance / genetics
  • Islets of Langerhans / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nuclear Receptor Subfamily 4, Group A, Member 1 / genetics
  • Paternal Exposure / adverse effects*
  • Scrotum / physiopathology*
  • Signal Transduction / genetics

Substances

  • Nr4a1 protein, mouse
  • Nuclear Receptor Subfamily 4, Group A, Member 1
  • Glucose