Microglia potentiate damage to blood-brain barrier constituents: improvement by minocycline in vivo and in vitro

Stroke. 2006 Apr;37(4):1087-93. doi: 10.1161/01.STR.0000206281.77178.ac. Epub 2006 Feb 23.

Abstract

Background: Blood-brain barrier (BBB) disruption after stroke can worsen ischemic injury by increasing edema and causing hemorrhage. We determined the effect of microglia on the BBB and its primary constituents, endothelial cells (ECs) and astrocytes, after ischemia using in vivo and in vitro models.

Methods and results: Primary astrocytes, ECs, or cocultures were prepared with or without added microglia. Primary ECs were more resistant to oxygen-glucose deprivation/reperfusion than astrocytes. ECs plus astrocytes showed intermediate vulnerability. Microglia added to cocultures nearly doubled cell death. This increase was prevented by minocycline and apocynin. In vivo, minocycline reduced infarct volume and neurological deficits and markedly reduced BBB disruption and hemorrhage in mice after experimental stroke.

Conclusions: Inhibition of microglial activation may protect the brain after ischemic stroke by improving BBB viability and integrity. Microglial inhibitors may prove to be an important treatment adjunct to fibrinolysis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetophenones / pharmacology
  • Animals
  • Antioxidants / pharmacology
  • Astrocytes / pathology
  • Blood-Brain Barrier / drug effects*
  • Brain / pathology
  • Brain Ischemia / complications
  • Brain Ischemia / metabolism
  • Brain Ischemia / pathology
  • Brain Ischemia / physiopathology*
  • Cell Death / drug effects
  • Cells, Cultured
  • Cerebral Hemorrhage / etiology
  • Cerebral Hemorrhage / physiopathology
  • Cerebral Infarction / pathology
  • Coculture Techniques
  • Endothelial Cells / pathology
  • Glucose / deficiency
  • Hydrogen Peroxide / metabolism
  • Hypoxia / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microglia* / drug effects
  • Microglia* / metabolism
  • Microglia* / pathology
  • Minocycline / pharmacology*
  • Nervous System Diseases / etiology
  • Nervous System Diseases / physiopathology
  • Superoxides / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Acetophenones
  • Antioxidants
  • Tumor Necrosis Factor-alpha
  • Superoxides
  • acetovanillone
  • Hydrogen Peroxide
  • Minocycline
  • Glucose