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The role of hypoxia-inducible factor-1α, aquaporin-4, and matrix metalloproteinase-9 in blood-brain barrier disruption and brain edema after traumatic brain injury: Laboratory investigation

Higashida, Tetsuhiro, Kreipke, Christian W., Rafols, José A., Peng, Changya, Schafer, Steven, Schafer, Patrick, Ding, Jamie Y., Dornbos, David, Li, Xiaohua, Guthikonda, Murali, Rossi, Noreen F., Ding, Yuchuan·2011·Journal of Neurosurgery

Abstract

Object: The present study investigated the role of hypoxia-inducible factor-1α (HIF-1α), aquaporin-4 (AQP-4), and matrix metalloproteinase-9 (MMP-9) in blood-brain barrier (BBB) permeability alterations and brain edema formation in a rodent traumatic brain injury (TBI) model. Methods: The brains of adult male Sprague-Dawley rats (400–425 g) were injured using the Marmarou closed-head force impact model. Anti–AQP-4 antibody, minocycline (an inhibitor of MMP-9), or 2-methoxyestradiol (2ME2, an inhibitor of HIF-1α), was administered intravenously 30 minutes after injury. The rats were killed 24 hours after injury and their brains were examined for protein expression, BBB permeability, and brain edema. Expression of HIF-1α, AQP-4, and MMP-9 as well as expression of the vascular basal lamina protein (laminin) and tight junction proteins (zona occludens-1 and occludin) was determined by Western blotting. Blood-brain barrier disruption was assessed by FITC-dextran extravasation, and brain edema was measured by the brain water content. Results: Significant (p < 0.05) edema and BBB extravasations were observed following TBI induction. Compared with sham-operated controls, the injured animals were found to have significantly (p < 0.05) enhanced expression of HIF-1α, AQP-4, and MMP-9, in addition to reduced amounts (p < 0.05) of laminin and tight junction proteins. Edema was significantly (p < 0.01) decreased after inhibition of AQP-4, MMP-9, or HIF-1α. While BBB permeability was significantly (p < 0.01) ameliorated after inhibition of either HIF-1α or MMP-9, it was not affected following inhibition of AQP-4. Inhibition of MMP reversed the loss of laminin (p < 0.01). Finally, while inhibition of HIF-1α significantly (p < 0.05) suppressed the expression of AQP-4 and MMP-9, such inhibition significantly (p < 0.05) increased the expression of laminin and tight junction proteins. Conclusions: The data support the notion that HIF-1α plays a role in brain edema formation and BBB disruption via a molecular pathway cascade involving AQP-4 and MMP-9. Pharmacological blockade of this pathway in patients with TBI may provide a novel therapeutic strategy.

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Metadata

Authors
Higashida, T., Kreipke, C. W., Rafols, J. A., Peng, C., Schafer, S., Schafer, P., Ding, J. Y., Dornbos, D., Li, X., Guthikonda, M., Rossi, N. F., & Ding, Y.
Venue
Journal of Neurosurgery
Published
2011-01
Volume
114
Issue
1
Pages
92-101
ISSN
  • 0022-3085 (ISSN-L)
  • 1933-0693
OpenAlex
W2163862018
Cited by
282
References
4
FWCI
10.27
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The role of hypoxia-inducible factor-1α, aquaporin-4, and matrix metalloproteinase-9 in blood-brain barrier disruption and brain edema after traumatic brain injury: Laboratory investigation. https://app.cochat.ai/papers/10.3171/2010.6.jns10207
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Higashida, T., Kreipke, C. W., Rafols, J. A., Peng, C., Schafer, S., Schafer, P., Ding, J. Y., Dornbos, D., Li, X., Guthikonda, M., Rossi, N. F., & Ding, Y. (2011). The role of hypoxia-inducible factor-1α, aquaporin-4, and matrix metalloproteinase-9 in blood-brain barrier disruption and brain edema after traumatic brain injury: Laboratory investigation. Journal of Neurosurgery. https://doi.org/10.3171/2010.6.jns10207

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