Maternal seizures can affect the brain developing of offspring

Ana Carolina Cossa1, Daiana Correia Lima2, Tiago Gurgel do Vale3

  • 1Departamento de Neurologia e Neurocirurgia - Disciplina de Neurologia Experimental, Universidade Federal de São Paulo, UNIFESP, Rua Pedro de Toledo, 669, 2° Andar, São Paulo, SP, Brasil. carol_cossa@hotmail.com.

Insights

Maternal epileptic seizures during pregnancy impair pup development, causing delayed growth, altered protein synthesis, and changes in apoptotic protein levels in the developing rat brain.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Toxicology

Background:

  • Maternal epilepsy and seizures can impact fetal development.
  • The effects of pilocarpine-induced seizures on the developing rat brain require further elucidation.

Purpose of the Study:

  • To investigate the impact of maternal pilocarpine-induced seizures on postnatal development in Wistar rats.
  • To analyze biochemical and developmental changes in pups exposed to maternal seizures in utero.

Main Methods:

  • Pilocarpine-induced seizures in pregnant Wistar rats.
  • Analysis of blood glucose and gases in pups within 24 hours of birth.
  • Measurement of protein synthesis using (14)C-leucine incorporation at postnatal day 1.
  • Western blot analysis of Bax, Bcl-2, and PARP-1 in the hippocampus from postnatal day 3 to 21.
  • Assessment of postnatal growth and developmental milestones.

Main Results:

  • Experimental pups exhibited compensated metabolic acidosis and hyperglycemia.
  • Reduced protein synthesis was observed in experimental pups at postnatal day 1.
  • Altered levels of pro-apoptotic (Bax) and anti-apoptotic (Bcl-2) proteins, along with PARP-1, were noted in the hippocampus during development.
  • A delay in postnatal growth, body weight gain, and developmental milestones was observed in experimental pups.

Conclusions:

  • Maternal epileptic seizures disrupt normal postnatal development in rat pups.
  • These disruptions include impaired protein synthesis, altered apoptotic protein expression, and delayed physical and neurological development.
  • The observed changes may stem from hormonal alterations, stress, or hypoxic events associated with maternal seizures during pregnancy.

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