LAUSR

Aeromedical evacuation-relevant hypobaria after traumatic brain injury (TBI) leads to increased neurologic injury and mortality in rats relative to those maintained under normobaria. However, applicability of rodent brain injury research to humans may be limited by differences in neuroanatomy. Therefore, we developed a model in which ferrets are exposed to polytrauma consisting of controlled cortical impact TBI and hemorrhagic shock subjected 24 h later to 6 h of hypobaria or normobaria. Our objective was to determine if the deleterious effects of hypobaria observed in rats, with lissencephalic brains, are also present in a species with a human-like gyrencephalic brain. While no mortality was observed, magnetic resonance spectroscopy (MRS) results obtained 2 days post-injury indicated reduced cortical creatine, N-acetylaspartate, GABA, myo-inositol, and glutamate which was not affected by hypobaria. T2-weighted magnetic resonance imaging (MRI) quantification revealed increased hyperintensity volume representing cortical edema at the site of impact following polytrauma. Hypobaria did not exacerbate this focal edema but did lead to overall reductions in total cortical volume. Both normobaric and hypobaric ferrets exhibited impaired spatial memory 6 days post-injury on the Object Location Test, but no differences were noted between groups. Finally, cortical lesion volume was not exacerbated by hypobaria exposure on day 7 post-injury. Results suggest that air travel 24 h after polytrauma is associated with structural changes in the ferret brain. Future studies should investigate secondary injury from hypobaria following polytrauma in greater detail including alternative outcome measures, timepoints, and exposure to multiple flights.