“…Immediately after baseline data collection, peritonitis was induced, and simultaneously animals were randomly assigned either to FiO 2 ϭ 0.21 (control group, n ϭ 10, 7 males/3 females, median body weight 51 [range 46 -59] kg), which was only modified thereafter to maintain arterial hemoglobin oxygen saturation Ն90%, or to 100% oxygen (hyperoxia group, n ϭ 10, 4 males/6 females, median body weight 51 [range 46 -58] kg), which was maintained until the end of the experiment. In accordance with literature reports (28,29) and pilot experiments, fecal peritonitis was induced by inoculating the autologous feces into the abdominal cavity through the drainage tubes, which were subsequently kept clamped for the following 12 hrs. Additional measurements were recorded at 12, 18, and 24 hrs of peritonitis.…”