Prolonged exposure to ketamine increases brain derived neurotrophic factor levels in developing rat brains

Curr Drug Saf. 2009 Jan;4(1):11-6. doi: 10.2174/157488609787354495.

Abstract

Prolonged exposure to ketamine, a NMDA receptor antagonist, results in accelerated neurodegeneration and attenuated weight gain in neonatal rats. Suppression of the NMDA receptors by non-competitive antagonists has resulted in conflicting reports of both increased and decreased expression of BDNF. To examine the effect of prolonged ketamine exposure on BDNF expression, we administered saline or ketamine (20 mg/kg) at 90-minute intervals over 9 hours to postnatal day 7 (P7) rat pups. The ketamine-treated rat pups had increased neurodegeneration, BDNF and TrkB cDNA products and protein levels. This increased expression of BDNF may be a response to ketamine-induced injury.

MeSH terms

  • Animals
  • Animals, Newborn
  • Brain-Derived Neurotrophic Factor / drug effects*
  • Brain-Derived Neurotrophic Factor / metabolism
  • DNA, Complementary / drug effects
  • DNA, Complementary / metabolism
  • Drug Administration Schedule
  • Excitatory Amino Acid Antagonists / administration & dosage
  • Excitatory Amino Acid Antagonists / toxicity*
  • Gene Expression Regulation / drug effects
  • Ketamine / administration & dosage
  • Ketamine / toxicity*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, trkB / drug effects*
  • Receptor, trkB / metabolism
  • Time Factors

Substances

  • Brain-Derived Neurotrophic Factor
  • DNA, Complementary
  • Excitatory Amino Acid Antagonists
  • Ketamine
  • Receptor, trkB