Lactational High-Fat Diet Exposure Programs Metabolic Inflammation and Bone Marrow Adiposity in Male Offspring

Nutrients. 2019 Jun 21;11(6):1393. doi: 10.3390/nu11061393.

Abstract

Overnutrition during critical windows of development plays a significant role in life-long metabolic disease risk. Early exposure to excessive nutrition may result in altered programming leading to increased susceptibility to obesity, inflammation, and metabolic complications. This study investigated the programming effects of high-fat diet (HFD) exposure during the lactation period on offspring adiposity and inflammation. Female C57Bl/6J dams were fed a normal diet or a 60% HFD during lactation. Offspring were weaned onto a normal diet until 12 weeks of age when half were re-challenged with HFD for 12 weeks. Metabolic testing was performed throughout adulthood. At 24 weeks, adipose depots were isolated and evaluated for macrophage profiling and inflammatory gene expression. Males exposed to HFD during lactation had insulin resistance and glucose intolerance as adults. After re-introduction to HFD, males had increased weight gain and worsened insulin resistance and hyperglycemia. There was increased infiltration of pro-inflammatory CD11c+ adipose tissue macrophages, and bone marrow was primed to produce granulocytes and macrophages. Bone density was lower due to enhanced marrow adiposity. This study demonstrates that maternal HFD exposure during the lactational window programs offspring adiposity, inflammation, and impaired glucose homeostasis.

Keywords: adipose tissue; developmental programming; inflammation; lactation; metabolism.

MeSH terms

  • Adipose Tissue / metabolism
  • Adipose Tissue / physiopathology*
  • Adiposity*
  • Age Factors
  • Animals
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Bone Marrow / metabolism
  • Bone Marrow / physiopathology*
  • Diet, High-Fat / adverse effects*
  • Female
  • Hyperglycemia / blood
  • Hyperglycemia / etiology*
  • Hyperglycemia / physiopathology
  • Inflammation / blood
  • Inflammation / etiology*
  • Inflammation / physiopathology
  • Inflammation Mediators / blood
  • Insulin Resistance
  • Lactation*
  • Male
  • Maternal Exposure / adverse effects*
  • Maternal Nutritional Physiological Phenomena*
  • Mice, Inbred C57BL
  • Myeloid Cells / metabolism
  • Nutritional Status
  • Obesity / blood
  • Obesity / etiology*
  • Obesity / physiopathology
  • Risk Factors
  • Sex Factors
  • Time Factors
  • Weight Gain

Substances

  • Biomarkers
  • Blood Glucose
  • Inflammation Mediators