Postnatal maternal care moderates the effects of prenatal bisphenol exposure on offspring neurodevelopmental,

Samantha C Lauby1,2, Hannah E Lapp1, Melissa Salazar1

  • 1Department of Psychology, College of Liberal Arts, University of Texas at Austin, Austin, Texas, United States of America.

Plos One
|June 11, 2024
PubMed

Insights

Prenatal exposure to bisphenols (BP) impacts neurodevelopment, but this effect depends on maternal care. Quality postnatal care can mitigate adverse outcomes from early-life BP exposure in rats.

Area of Science:

  • Endocrinology
  • Neuroscience
  • Developmental Biology

Background:

  • Bisphenols (BP), including BPA and "BPA-free" analogs, are endocrine-disrupting chemicals found in plastics.
  • Prenatal BPA exposure is linked to adverse neurodevelopmental and behavioral outcomes, and impaired maternal care.
  • Limited data exists on non-BPA bisphenols and the combined effects of prenatal BP exposure and postnatal maternal care.

Purpose of the Study:

  • To investigate the interactive impact of prenatal bisphenol exposure and postnatal maternal care on rat neurodevelopment and behavior.
  • To explore the underlying molecular mechanisms, including transcriptomic changes.

Main Methods:

  • Rats were exposed to bisphenols prenatally.
  • Postnatal maternal care was assessed in the first five days of life.
  • Neurodevelopmental (eye-opening) and adult behaviors (attentional set shifting, anxiety) were evaluated.
  • Transcriptomic profiling of medial prefrontal cortex and amygdala was performed.

Main Results:

  • Prenatal bisphenol exposure effects on eye-opening, attention, and anxiety were modulated by maternal care.
  • Maternal care may attenuate some adverse effects of prenatal bisphenol exposure.
  • Transcriptomic data indicated convergence on estrogen receptor signaling and gene expression pathways.

Conclusions:

  • Postnatal maternal care is crucial in mediating the neurodevelopmental and behavioral effects of prenatal bisphenol exposure.
  • Understanding these interactions may reveal strategies to mitigate adverse bisphenol effects.
  • Estrogen receptor signaling and gene expression are key biological pathways involved.