Teratogenic effects of retinoic acid on neurulation in mice embryos

M Nobakht1, A Zirak, M Mehdizadeh

  • 1Department of Anatomy and Histology, Iran University Of Medical Sciences, P.O. Box 14155-6183, Tehran, Iran. nobakht@yahoo.com

Insights

High doses of all-trans retinoic acid (RA) cause significant birth defects in mouse embryos, particularly affecting central nervous system (CNS) development. RA exposure disrupted neural tube closure and disorganized developing brain structures.

Area of Science:

  • Developmental Biology
  • Neuroscience
  • Toxicology

Background:

  • Retinoic acids (RA) are crucial signaling molecules regulating embryonic development.
  • Aberrant RA signaling is implicated in various congenital malformations.

Purpose of the Study:

  • To investigate the teratogenic effects of all-trans retinoic acid (RA) on the developing central nervous system (CNS) in mouse embryos.
  • To determine dose-dependent effects of RA on neural tube closure and neuroepithelial organization.

Main Methods:

  • Pregnant mice were administered varying doses of all-trans RA (40 and 60 mg/kg) or vehicle (DMSO) on day 8 of gestation.
  • Embryos were examined for malformations, size, neural tube closure, and histological changes in CNS layers.

Main Results:

  • RA exposure led to embryo malformations and reduced size.
  • Significant dose-dependent inhibition of neural tube closure was observed (50% closure at 40 mg/kg, failure at 60 mg/kg).
  • Histological analysis revealed disorganized neuroblast layers, increased chromatin density, reduced layer thickness, intercellular spaces, and fluid accumulation.

Conclusions:

  • All-trans retinoic acid exhibits potent teratogenic effects on the developing CNS in mice.
  • RA disrupts critical developmental processes including neural tube formation and neuroepithelial structure.
  • These findings highlight the sensitivity of early embryonic development to retinoic acid signaling.