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.
|
Authors | Lisa C Hutton, Mahila Abbass, Hayley Dickinson, Zoe Ireland, David W Walker |
Journal | Developmental neuroscience
(Dev Neurosci)
Vol. 31
Issue 5
Pg. 437-51
( 2009)
ISSN: 1421-9859 [Electronic] Switzerland |
PMID | 19684403
(Publication Type: Journal Article)
|
Copyright | (c) 2009 S. Karger AG, Basel. |
Chemical References |
|
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
|