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      Postresuscitation treatment with argon improves early neurological recovery in a porcine model of cardiac arrest.

      Shock (Augusta, Ga.)

      Sus scrofa, Animals, therapeutic use, Neuroprotective Agents, pathology, complications, Myocardial Infarction, Male, Hippocampus, physiology, Hemodynamics, therapy, physiopathology, Heart Arrest, methods, Drug Evaluation, Preclinical, Disease Models, Animal, Combined Modality Therapy, Cardiopulmonary Resuscitation, prevention & control, etiology, Brain Ischemia, Argon, Treatment Outcome

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          Abstract

          Effects of postresuscitation treatment with argon on neurologic recovery were investigated in a porcine model of cardiac arrest (CA) with an underlying acute myocardial infarction. The left anterior descending coronary artery was occluded in 12 pigs, and CA was induced. After 8 min of untreated CA, cardiopulmonary resuscitation was performed for 5 min before defibrillation. Following resuscitation, animals were subjected to 4-h ventilation with 70% argon/30% oxygen or 70% nitrogen/30% oxygen. Myocardial function was echocardiographically assessed, and serum neuron-specific enolase was measured. Animals were observed up to 72 h for assessment of survival and neurologic recovery. All the animals were resuscitated and survived for 72 h, except for a control pig. Ventilation with argon did not have any detrimental effects on hemodynamics and respiratory gas exchange. All the six argon-treated animals had a fast and complete 72-h neurologic recovery, in contrast to only two of the six controls (P < 0.05). Seventy-two-hour neurologic alertness score and neurologic deficit score were, respectively, 100 and 0 in the argon group and 79 and 29 in the control one (P < 0.01 and P < 0.05). Significantly lower increases in serum neuron-specific enolase (12% vs. 234%) and minimal histological brain injury (neuronal degeneration: 0 vs. 1) were also observed in argon-treated animals, in comparison to controls. In this model, postresuscitation treatment with argon allowed for a faster and complete neurologic recovery, without detrimental effects on hemodynamics and respiratory gas exchanges.

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          Journal
          10.1097/SHK.0000000000000049
          24088999

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