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Updated: Jun 23, 2026
The Hypoxic Ischemic Encephalopathy Model of Perinatal Ischemia
Published on: November 19, 2008
HIF-1 alpha inhibition ameliorates neonatal brain damage after hypoxic-ischemic injury
Wanqiu Chen1, Vikram Jadhav, Jiping Tang
1Department of Physiology and Pharmacology, Loma Linda University Medical Center, Risley Hall, Room 214, Loma Linda, CA 92354, USA.
Background:
Hypoxia-inducible-factor-1alpha (HIF-1alpha) has been considered as a regulator of both prosurvival and prodeath pathways in the nervous system. This study was designed to elucidate the role of HIF-1alpha in neonatal hypoxia-ischemia (HI) brain injury.
Methods:
2-methoxyestradiol (2ME2), a HIF-1alpha inhibitor, was tested at different dosages (1.5, 15 and 150 mg/kg) and a therapeutic window was tested by administrating 2-methoxyestradiol (15 mg/kg) immediately or 3 hours after the induction of a hypoxic ischemic injury. Infarct size using TTC staining and brain edema were measured at 48 hours post hypoxia-ischemia. Blood-brain barrier (BBB) permeability was examined by IgG staining. Vascular endothelial growth factor (VEGF) and HIF-1alpha expression and distribution were studied by immunohistochemistry and western blotting analysis.
Findings:
2ME2 exhibited dose-dependent neuroprotection by decreasing infarct volume and attenuating brain edema. 2ME2 also attenuated BBB disruption, and decreased HIF-1alpha and vascular endothelial growth factor (VEGF) expression. The neuroprotection, however, was lost when 2ME2 was administered 3 hours after neonatal HI.
Conclusion:
The study shows that the acute inhibition of HIF-1alpha is neuroprotective in neonatal hypoxic-ischemic injury by preserving BBB integrity and reducing brain edema.
