Artificial Dim Light at Night during Pregnancy Can Affect Hormonal and Metabolic Rhythms in Rat Offspring

Zuzana Dzirbíková1, Katarína Stebelová1, Katarína Kováčová1

  • 1Department of Animal Physiology and Ethology, Faculty of Natural Sciences, Comenius University, Ilkovičova 6, 842 15 Bratislava, Slovakia.

Insights

Artificial light at night (ALAN) during pregnancy disrupts hormone rhythms in rat pups. This exposure can interfere with normal endocrine development and metabolism in offspring.

Area of Science:

  • Endocrinology
  • Environmental Health
  • Developmental Biology

Background:

  • Artificial light at night (ALAN) is an emerging environmental risk factor.
  • ALAN can disrupt circadian rhythms, impacting endocrine and metabolic systems.
  • The effects of prenatal ALAN exposure on offspring development require further investigation.

Purpose of the Study:

  • To investigate the impact of maternal exposure to artificial light at night (ALAN) during pregnancy on hormonal and biochemical parameters in rat pups.
  • To assess the developmental effects of ALAN on circadian rhythms of hormones and metabolites in offspring.

Main Methods:

  • Controlled study exposing pregnant rats to dim ALAN (<2 lx) or standard light-dark cycles.
  • Measurement of plasma melatonin, corticosterone, thyroid hormones, vasopressin, glucose, and cholesterol in offspring at postnatal days P3, P10, and P20.
  • Analysis of daily rhythms and specific hormonal/metabolic parameters.

Main Results:

  • ALAN exposure disrupted melatonin rhythms in pups at P3 and P10.
  • Reduced corticosterone mesor and suppressed vasopressin levels were observed in ALAN-exposed pups at P20.
  • Daily rhythms of glucose and cholesterol were absent in ALAN pups at P3.
  • ALAN exposure impaired the development of hormonal and metabolic daily rhythms.

Conclusions:

  • Prenatal exposure to artificial light at night acts as an endocrine disruptor.
  • ALAN during pregnancy interferes with the normal development of circadian rhythms in hormones and metabolites in offspring.
  • These disruptions suggest potential long-term health implications for progeny exposed to ALAN in utero.