Journal
JOURNAL OF PSYCHIATRY & NEUROSCIENCE
Volume 35, Issue 1, Pages 20-32Publisher
CMA-CANADIAN MEDICAL ASSOC
DOI: 10.1503/jpn.090061
Keywords
-
Categories
Funding
- Davey Fund
- Heart and Stroke Foundation of Canada
- Canadian Stroke Network
- Stollery Children's Hospital Foundation
- Canadian Institutes of Health Research
- Natural Science and Engineering Research Council of Canada
- Alberta Heritage Foundation for Medical Research
Ask authors/readers for more resources
Background: Neonatal hypoxia-ischemia (HI) is a major cause of perinatal brain injury and is associated with a spectrum of neuropsychiatric disorders. Although very few treatment options are currently available, doxycycline (DOXY) has been reported to be neuroprotective in neontatal HI. Our objective was to investigate the effects of DOXY on neonatal brain development in normal and HI rat pups. We hypothesized that DOXY would inhibit microglial activation but that developmentally important processes, including cytogenesis and trophic responses, would not be impaired. Methods: To investigate the putative neurodevelopmental consequences of DOXY administration in a clinically relevant animal model of HI, we performed a time-course analysis such that postnatal rat pups received DOXY (10 mg/kg) or vehicle immediately before HI (n >= 6). We then assessed cytogenesis, proinflammatory cytokines, brain-derived neurotrophic factor (BDNF) and matrix metalloproteinases regionally and longitudinally. Results: We found that DOXY significantly inhibits neuroinflammation in the frontal cortex, striatum and hippocampus; decreases interleukin-1 beta (IL-1 beta) and tumour necrosis factor-alpha (TNF-alpha); and augments BDNF following HI. In addition, DOXY-treated pups have significantly fewer 2-bromo-5-deoxyuridine (BrdU)positive cells in the subventricular zone 6 hours post-HI. However, DOXY does not persistently affect cytogenesis in the subventricular zone or dentate gyrus up to 7 days post-HI. The BrdU-positive cells not expressing markers for mature neurons colabel with nestin, an intermediate filament protein typical of neuronal precursors. Limitations: Our study investigates acute neurodevelopment over the first 7 days of life after HI injury. Further long-term investigations into adulthood are underway. Conclusion: Taken together, our results suggest the putative clinical potential of DOXY in the management of neonatal cerebral HI injury.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available