The effects of repeated corticosteroid administration on the neurogenesis in the neonatal rat

Am J Obstet Gynecol. 2006 Jan;194(1):231-8. doi: 10.1016/j.ajog.2005.06.015.

Abstract

Objective: The purpose of this study is to clarify the effects on the brain including neurogenesis pretreated with repeated doses of dexamethasone in the neonatal rat.

Study design: The 4-day-old Sprague Dawley rats were pretreated with 4 different regimens, namely, single administration of dexamethasone, 2-dose administration, 3-dose administration, and saline administration as a control. Concurrently, bromodeoxyuridine (BrdU), which was incorporated into the dividing cells, was administered. We examined body weight, brain weight, and the number of BrdU-labeled cells in the subventricular zone (SVZ), the subgranular zone (SGZ), and the cortex.

Results: Both the body and brain weight of the rats pretreated with dexamethasone were significantly decreased compared with those given saline. Quantitative analysis of BrdU-labeled cells revealed the significant dose-dependent decreases in the SVZ, the SGZ, and the cortex with the dexamethasone treatment.

Conclusion: We concluded that the decreases in neurogenesis caused by repeated antenatal corticosteroid therapy might result in the adverse effects on the size of the head at birth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Animals
  • Animals, Newborn / growth & development*
  • Body Weight / drug effects
  • Brain / cytology
  • Brain / drug effects*
  • Brain / growth & development*
  • Brain / metabolism
  • Bromodeoxyuridine / pharmacokinetics
  • Cell Proliferation / drug effects
  • DNA-Binding Proteins
  • Dexamethasone / administration & dosage*
  • Dexamethasone / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Immunohistochemistry
  • Mitosis
  • Nerve Tissue Proteins / metabolism
  • Nuclear Proteins / metabolism
  • Phenotype
  • Rats
  • Rats, Sprague-Dawley

Substances

  • DNA-Binding Proteins
  • Nerve Tissue Proteins
  • NeuN protein, mouse
  • Nuclear Proteins
  • Dexamethasone
  • Bromodeoxyuridine