Exposure to PCB126 during the nursing period reversibly impacts early-life glucose tolerance

Brittany B Rice1, Keegan W Sammons1, Sara Y Ngo Tenlep1

  • 1Department of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, KY, United States.

Insights

Exposure to polychlorinated biphenyls (PCBs) via nursing impairs offspring glucose tolerance temporarily. PCB126 exposure did not affect body composition in mice, but short-term glucose intolerance was observed.

Area of Science:

  • Environmental Toxicology
  • Developmental Toxicology
  • Endocrinology

Background:

  • Polychlorinated biphenyls (PCBs) are persistent environmental pollutants with known adverse health effects.
  • Previous studies showed PCB126 exposure during gestation and perinatal periods impacts offspring glucose tolerance and body composition.
  • The effects of PCB exposure solely during the nursing period on offspring metabolic health remain less understood.

Purpose of the Study:

  • To investigate the impact of PCB126 exposure during the nursing period on offspring glucose tolerance and body composition.
  • To determine if maternal exposure to PCB126 via milk affects offspring metabolic profiles.

Main Methods:

  • Female ICR mice were exposed to PCB126 (1 µmole/kg) or vehicle via oral gavage on postnatal days 3, 10, and 17.
  • Offspring body weight, lean and fat mass, and glucose tolerance were assessed every three weeks.
  • Statistical analyses were performed to compare outcomes between PCB126-exposed and control groups.

Main Results:

  • PCB126 exposure did not significantly alter dam or offspring body weight or body composition.
  • Offspring exposed to PCB126 during nursing exhibited significantly impaired glucose tolerance at 3 and 9 weeks of age.
  • Glucose tolerance returned to normal levels by 6 and 12 weeks of age, indicating a short-term effect.

Conclusions:

  • Maternal exposure to PCB126 during the nursing period does not affect offspring body composition.
  • Short-term glucose intolerance is a consequence of PCB126 exposure via maternal milk.
  • These findings highlight the critical window of the nursing period for PCB-induced metabolic disruption.

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