Prenatal polycyclic aromatic hydrocarbon, adiposity, peroxisome proliferator-activated receptor (PPAR) γ methylation in offspring, grand-offspring mice

PLoS One. 2014 Oct 27;9(10):e110706. doi: 10.1371/journal.pone.0110706. eCollection 2014.

Abstract

Rationale: Greater levels of prenatal exposure to polycyclic aromatic hydrocarbon (PAH) have been associated with childhood obesity in epidemiological studies. However, the underlying mechanisms are unclear.

Objectives: We hypothesized that prenatal PAH over-exposure during gestation would lead to weight gain and increased fat mass in offspring and grand-offspring mice. Further, we hypothesized that altered adipose gene expression and DNA methylation in genes important to adipocyte differentiation would be affected.

Materials and methods: Pregnant dams were exposed to a nebulized PAH mixture versus negative control aerosol 5 days a week, for 3 weeks. Body weight was recorded from postnatal day (PND) 21 through PND60. Body composition, adipose cell size, gene expression of peroxisome proliferator-activated receptor (PPAR) γ, CCAAT/enhancer-binding proteins (C/EBP) α, cyclooxygenase (Cox)-2, fatty acid synthase (FAS) and adiponectin, and DNA methylation of PPAR γ, were assayed in both the offspring and grand-offspring adipose tissue.

Findings: Offspring of dams exposed to greater PAH during gestation had increased weight, fat mass, as well as higher gene expression of PPAR γ, C/EBP α, Cox2, FAS and adiponectin and lower DNA methylation of PPAR γ. Similar differences in phenotype and DNA methylation extended through the grand-offspring mice.

Conclusions: Greater prenatal PAH exposure was associated with increased weight, fat mass, adipose gene expression and epigenetic changes in progeny.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adipocytes / cytology
  • Adiponectin / genetics
  • Adiponectin / metabolism
  • Adiposity / drug effects*
  • Adiposity / genetics*
  • Animals
  • Body Weight / genetics
  • CCAAT-Enhancer-Binding Proteins / genetics
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Cell Size
  • CpG Islands
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • DNA Methylation*
  • Disease Models, Animal
  • Female
  • Gene Expression
  • Maternal Exposure*
  • Mice
  • PPAR gamma / genetics*
  • PPAR gamma / metabolism
  • Pediatric Obesity / etiology
  • Pediatric Obesity / metabolism
  • Phenotype
  • Polycyclic Aromatic Hydrocarbons / adverse effects*
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • fas Receptor / genetics
  • fas Receptor / metabolism

Substances

  • Adiponectin
  • CCAAT-Enhancer-Binding Proteins
  • PPAR gamma
  • Polycyclic Aromatic Hydrocarbons
  • fas Receptor
  • Cyclooxygenase 2