Paraplegia after
thoracic aortic aneurysm repair has an incidence of 2.2% to 24%.
Oxygen-derived
free radicals after reperfusion of an ischemic spinal cord may be partly responsible for neuronal destruction. We studied the effects of
polyethylene glycol-conjugated
superoxide dismutase (
PEG-SOD), a
free radical scavenger, as a way of increasing spinal cord tolerance to
ischemia. Thirty rabbits underwent 40 minutes of aortic occlusion (a known model of
paraplegia). Ten of these animals received 25,000 U/kg of
PEG-SOD 24 hours before aortic occlusion and two additional doses of 10,000 U/kg, one before and one subsequent to spinal
ischemia. Ten animals received
superoxide dismutase in the same dosages as those receiving
PEG-SOD. Ten control animals received placebo. All animals were studied for 96 hours, at which time a final neurological examination was performed and the results were recorded. Of the 10 animals treated with
PEG-SOD, 2 were completely paralyzed whereas 8 had less (7) or no (1) neurological impairment. Eight of the 10 control animals and 9 of the 10 animals receiving
superoxide dismutase were completely paralyzed. None of the control animals or animals receiving
superoxide dismutase had a normal neurological examination (p less than or equal to 0.05). Treatment with
PEG-SOD before and during occlusion increased the rabbit spinal cord tolerance to a 40-minute ischemic insult. Scavenging
free radicals may lessen experimental
spinal cord injury.