This study was designed to test the hypothesis that propofol, which po
ssesses antioxidant properties, would produce greater protection than
isoflurane in cerebral ischaemia reperfusion injury, at dose levels th
at produced similar effects on brain electrical activity. Twenty Sprag
ue-Dawley rats were anaesthetized using isoflurane 1.5% in air/oxygen,
and mechanically ventilated to a PaCO2 of 4.5 kPa. Following 90 min o
f middle cerebral artery occlusion using an intraluminal filament, rat
s were given, in random order, either propofol 1 mg kg(-1) min(-1) or
isoflurane 3% (both of which have been shown to reliably produce EEG b
urst suppression). After a further 30 min, reperfusion was induced by
withdrawing the filament. Animals were killed following 240 min of rep
erfusion. Rats in the propofol group showed a 21% reduction in mean he
mispheric infarct volume when compared with the isoflurane group (P<0.
0001). These data suggest that propofol may act by mechanisms in addit
ion to CMRO2 depression, and provide a basis for further studies of pr
opofol neuroprotection.