Therapeutic hypothermia attenuates physiologic, histologic, and metabolomic markers of injury in a porcine model of acute respiratory distress syndrome

Acute respiratory distress syndrome (ARDS) is a lung injury characterized by non-cardiogenic pulmonary edema and hypoxic respiratory failure. The purpose of this study was to investigate the effects of therapeutic hypothermia on short-term experimental ARDS. 'Twenty adult female Yorkshire pigs were divided into four groups (n = 5 each): normothermic control (C), normothermic injured (I), hypothermic control (HC), and hypothermic injured (HI). Acute respiratory distress syndrome was induced experimentally via intrapulmonary injection of oleic acid. Target core temperature was achieved in the HI group within 1 h of injury induction. Cardiorespiratory, histologic, cytokine, and metabolomic data were collected on all animals prior to and following injury/sham. All data were collected for approximately 12 h from the beginning of the study until euthanasia. Therapeutic hypothermia reduced injury in the III compared to the I group (histological injury score = 0.51 +/- 0.18 vs. 0.76 +/- 0.06; p = 0.02) with no change in gas exchange. All groups expressed distinct phenotypes, with a reduction in pro-inflammatory metabolites, an increase in anti-inflammatory metabolites, and a reduction in inflammatory cytokines observed in the HI group compared to the I group. Changes to respiratory system mechanics in the injured groups were due to increases in lung elastance (E) and resistance (R) Delta E from pre-injury = 46 +/- 14 cmH(2)O L-1, p < 0.0001; Delta R from pre-injury: 3 +/- 2 cmH(2)O L-1 s(-), p = 0.30) rather than changes to the chest wall (Delta E from pre-injury: 0.7 +/- 1.6 cmH(2)O L-1, p = 0.99; Delta R from pre-injury: 0.6 +/- 0.1 cmH(2)O L-1 s(-), p = 0.01). Both control groups had no change in respiratory mechanics. In conclusion, therapeutic hypothermia can reduce markers of injury and inflammation associated with experimentally induced short-term ARDS.

Automated summary

Therapeutic hypothermia can reduce injury and inflammation associated with experimentally induced short-term ARDS. Gas exchange was not affected. The hypothermic injured group showed a reduction in pro-inflammatory metabolites, an increase in anti-inflammatory metabolites, and a reduction in inflammatory cytokines compared to the normothermic injured group.