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Sevoflurane protects rat brain endothelial barrier structure and function after hypoxia-reoxygenation injury.

Sevoflurane protects rat brain endothelial barrier structure and function after hypoxia-reoxygenation injury.
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Restin T, Kajdi ME, Schläpfer M, Roth Z'graggen B, Booy C, Dumrese C, Beck-Schimmer B,


Restin T, Kajdi ME, Schläpfer M, Roth Z'graggen B, Booy C, Dumrese C, Beck-Schimmer B, (click to view)

Restin T, Kajdi ME, Schläpfer M, Roth Z'graggen B, Booy C, Dumrese C, Beck-Schimmer B,

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PloS one 2017 10 1212(10) e0184973 doi 10.1371/journal.pone.0184973
Abstract
BACKGROUND
After cerebral injury blood-brain barrier disruption significantly impairs brain homeostasis. Volatile anesthetics have been shown to be protective in ischemia-reperfusion injury scenarios. Their impact on brain endothelial cells after hypoxia-reoxygenation (H/R) has not yet been studied in detail.

METHODS
Rat brain endothelial cells (RBE4) were exposed to severe hypoxia and reoxygenated in air in the presence or absence of sevoflurane. Changes in dextran permeability and architecture of the cellular junctional proteins ZO-1 and β-catenin were measured. To determine necrosis and apoptosis rate DNA content, LDH release and caspase activity were quantified. The role of vascular endothelial growth factor (VEGF) as an inflammatory mediator increasing vascular permeability was assessed. At the same time, it was evaluated if sevoflurane effects are mediated through VEGF. Results were analyzed by unpaired t-tests or one way-analysis of variance followed by Bonferroni’s correction.

RESULTS
H/R led to a 172% increase in permeability (p<0.001), cell swelling and qualitatively but not quantitatively modified expression of ZO-1, β-catenin and F-actin. In the presence of sevoflurane during reoxygenation, barrier function improved by 96% (p = 0.042) in parallel to a decrease of the cell size and less re-arranged junction proteins and F-actin. Sevoflurane-induced improvement of the barrier function could not be explained on the level of necrosis or apoptosis as they remained unchanged independent of the presence or absence of the volatile anesthetic. Increased expression of VEGF after H/R was attenuated by sevoflurane by 34% (p = 0.004). Barrier protection provided by sevoflurane was similar to the application of a blocking VEGF-antibody. Furthermore, the protective effect of sevoflurane was abolished in the presence of recombinant VEGF. CONCLUSIONS
In H/R-induced rat brain endothelial cell injury sevoflurane maintains endothelial barrier function through downregulation of VEGF, which is a key player not only in mediating injury, but also with regard to the protective effect of sevoflurane.

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