Protection against hypoxia-induced blood-brain barrier disruption: Changes in intracellular calcium

Rachel C. Brown, Karen S. Mark, Richard D. Egleton, Thomas P. Davis

Research output: Contribution to journalArticlepeer-review

45 Scopus citations


Tissue damage after stroke is partly due to disruption of the blood-brain barrier (BBB). Little is known about the role of calcium in modulating BBB disruption. We investigated the effect of hypoxic and aglycemic stress on BBB function and intracellular calcium levels. Bovine brain microvessel endothelial cells were treated with A-23187 to increase intracellular calcium without hypoxia or treated with a calcium chelator (BAPTA) or calcium channel blockers (nifedipine or SKF-96365) and 6 h of hypoxia. A-23187 alone did not increase paracellular permeability. Hypoxia increased intracellular calcium, and hypoxia or hypoxia-aglycemia increased paracellular permeability. Treatment with nifedipine and SKF-96365 increased intracellular calcium under normoglycemic conditions, instead of blocking calcium influx, and was protective against hypoxia-induced BBB disruption under normoglycemia. Protection by nifedipine and SKF-96365 was not due to antioxidant properties of these compounds. These data indicate that increased intracellular calcium alone is not enough to disrupt the BBB. However, increased intracellular calcium after drug treatment and hypoxia suggests a potential mechanism for these drugs in BBB protection; nifedipine and SKF-96365 plus hypoxic stress may trigger calcium-mediated signaling cascades, altering BBB integrity.

Original languageEnglish (US)
Pages (from-to)C1045-C1052
JournalAmerican Journal of Physiology - Cell Physiology
Issue number5 55-5
StatePublished - May 2004


  • Fura 2
  • Ischemia
  • Nifedipine
  • Permeability
  • SKF-96365

ASJC Scopus subject areas

  • Physiology
  • Cell Biology


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