Publication | Open Access
Hydrogen Sulfide Inhalation Decreases Early Blood—Brain Barrier Permeability and Brain Edema Induced by Cardiac Arrest and Resuscitation
61
Citations
30
References
2014
Year
Acute Lung InjuryTraumatic Brain InjuryHydrogen Sulfide InhalationPrehospital ResuscitationOxidative StressIntegrative PhysiologyCerebral Vascular RegulationCardiopulmonary ResuscitationClinical InjuryBrain InjuryHealth SciencesVentricular FibrillationHypoxia (Medicine)Vascular BiologyNeuroprotectionCerebral Blood FlowReperfusion InjuryNeurological AssessmentHydrogen SulfideBrain Edema InducedCardiac ArrestNeurophysiologyPhysiologyTissue OxygenationMedicine
The effects of hydrogen sulfide (H 2 S) on blood—brain barrier (BBB) and brain edema after cardiac arrest (CA) and cardiopulmonary resuscitation (CPR) remain poorly understood. We investigated the effects of exogenous 80-p.p.m. H 2 S gas on BBB, brain water content, neurologic outcome, and survival rate after CA and CPR. Cardiopulmonary resuscitation followed CA induced in rats by ventricular fibrillation for 6 minutes. Results show that inhalation of 80-p.p.m. H 2 S significantly reduced the permeability of the BBB in both in the cortex and hippocampus at 24 hours after resuscitation. Hydrogen sulfide also lessened brain edema in the cortex and hippocampus, ameliorated neurologic outcome as evaluated by neurologic deficit score and tape removal test, and improved the 14-day survival rate. Hydrogen sulfide also attenuated CA and CPR-induced increases of matrix metalloproteinase-9 (MMP-9) activity and vascular endothelial growth factor (VEGF) expression, and increased the expression of angiogenin-1 (Ang-1). These results indicate that inhalation of 80-p.p.m. H 2 S immediately after CPR attenuated BBB permeability and brain edema, and improved neurologic outcome and 14-day survival of rats after CA. The therapeutic benefits of H 2 S could be associated with suppression of MMP-9 and VEGF expression and increased expression of Ang-1.
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