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Neuroprotective properties of melatonin in a model of birth asphyxia in the spiny mouse (Acomys cahirinus).

Abstract
Birth asphyxia is associated with disturbed development of the neonatal brain. In this study, we determined if low-dose melatonin (0.1 mg/kg/day), administered to the mother over 7 days at the end of pregnancy, could protect against the effects of birth asphyxia in a precocial species - the spiny mouse (Acomys cahirinus). At 37 days of gestation (term is 38-39 days), pups were subjected to birth asphyxia (7.5 min uterine ischemia) and compared to Cesarean section-delivered controls. At 24 h of age, birth asphyxia had increased markers of CNS inflammation (microglia, macrophage infiltration) and apoptosis (activated caspase-3, fractin) in cortical gray matter, which were reduced to control levels by prior maternal melatonin treatment. Melatonin may be an effective prophylactic agent for use in late pregnancy to protect against hypoxic-ischemic brain injury at birth.
AuthorsLisa C Hutton, Mahila Abbass, Hayley Dickinson, Zoe Ireland, David W Walker
JournalDevelopmental neuroscience (Dev Neurosci) Vol. 31 Issue 5 Pg. 437-51 ( 2009) ISSN: 1421-9859 [Electronic] Switzerland
PMID19684403 (Publication Type: Journal Article)
Copyright(c) 2009 S. Karger AG, Basel.
Chemical References
  • Caspase 3
  • Melatonin
Topics
  • Analysis of Variance
  • Animals
  • Animals, Newborn
  • Apoptosis
  • Caspase 3 (metabolism)
  • Cell Count
  • Cerebral Cortex (metabolism, pathology)
  • Cytoprotection
  • Female
  • Hypoxia-Ischemia, Brain (drug therapy, pathology)
  • Immunohistochemistry
  • Infusion Pumps, Implantable
  • Macrophage Activation
  • Melatonin (administration & dosage, blood, therapeutic use)
  • Microglia (metabolism)
  • Murinae
  • Neurons (metabolism, pathology)
  • Oligodendroglia (metabolism, pathology)
  • Pregnancy
  • Prenatal Exposure Delayed Effects (metabolism)
  • Radioimmunoassay
  • Staining and Labeling

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