Maternal high-fat diet alters thermogenic markers but not muscle or brown adipose cannabinoid receptors in adult rats

Life Sci. 2022 Oct 1:306:120831. doi: 10.1016/j.lfs.2022.120831. Epub 2022 Jul 23.

Abstract

Aims: The endocannabinoid system (ECS) increases food intake, appetite for fat and lipogenesis, while decreases energy expenditure (thermogenesis), contributing to metabolic dysfunctions. We demonstrated that maternal high-fat diet (HFD) alters cannabinoid signaling in brown adipose tissue (BAT) of neonate and weanling male rat offspring, which have increased adiposity but also higher energy expenditure in adulthood. In this study, the main objective was to investigate the ECS expression in thermogenic tissues as BAT and skeletal muscle of adult rats programmed by maternal HFD. We hypothesized that maternal HFD would modulate ECS and energy metabolism markers in BAT and skeletal muscle of adult male offspring.

Materials and methods: Female rats received standard diet (9.4 % of calories as fat) or isocaloric HFD (28.9 % of calories as fat) for 8 weeks premating and throughout gestation and lactation. Male offspring were weaned on standard diet and euthanatized in adulthood.

Key findings: Maternal HFD increased body weight, adiposity, glycemia, leptinemia while decreased testosterone levels in adult offspring. Maternal HFD did not change cannabinoid receptors in BAT or skeletal muscle as hypothesized but increased the content of uncoupling protein and tyrosine hydroxylase (thermogenic markers) in parallel to changes in mitochondrial morphology in skeletal muscle of adult offspring.

Significance: In metabolic programming models, the ECS modulation in the BAT and skeletal muscle may be more important early in life to adapt energy metabolism during maternal dietary insult, and other mechanisms are possibly involved in muscle metabolism long-term regulation.

Keywords: Brown adipose tissue; Endocannabinoid system; Maternal high-fat diet; Skeletal muscle; Thermogenesis.

MeSH terms

  • Adipose Tissue, Brown / metabolism
  • Adiposity
  • Animals
  • Diet, High-Fat* / adverse effects
  • Endocannabinoids / metabolism
  • Female
  • Male
  • Obesity / metabolism
  • Rats
  • Receptors, Cannabinoid
  • Thermogenesis*

Substances

  • Endocannabinoids
  • Receptors, Cannabinoid