SUMMARY Twenty-four cats had an intravenous infusion of either Fluosol or saline and then were subjected to 2 hours of middle cerebral artery occlusion. All the animals infused with Fluosol and one-half the animals infused with saline were ventilated with 100% O 2 . Tissue oxygen availability and regional cerebral blood flow were measured by platinum electrodes using direct voltage recordings for oxygen measurements and hydrogen clearance curves for measurements of cerebral blood flow. With 100% oxygenation tissue oxygen availability increased significantly in the Fluosol treated animals, however, during the time of ischemia oxygen availability decreased below baseline values to about an equal level whether the animals were treated with Fluosol or saline. Regional cerebral blood flow fell to a similar value in all groups during the time of occlusion. One hour after reperfusion blood flow increased considerably above baseline values in all groups and oxygen availability also increased in all groups but particularly in the Fluosol treated animals. Overall mortality and the size of infarction 1 week after the ischemic insult were not significantly different in the three groups. Mortality was directly related to the size of the infarct which, in turn, was related to the degree of ischemia during the time of occlusion.
Stroke Vol 17, No 5, 1986PERFLUOROCHEMICALS (PFC), or fluorocarbons, are inert organic compounds capable of substituting for the gas transport functions of blood because of their high affinity for O 2 and CO 2 . lJ) In acute experiments in other laboratories, as well as in ours, they have been shown to be useful in protecting the brain from the effects of ischemia. 4 "* In another study where cats were sacrificed 24 hours after occlusion of one middle cerebral artery (MCA), PFC also seemed of value although their effect was not as beneficial as in the acute experiments.7 However, in a more "chronic" study where cats were treated either with PFC or with dextran and were kept alive for one week after a 4-hour period of MCA occlusion, we failed to show any benefit from either agent and there was a high mortality from cerebral infarction in both groups (unpublished data). We concluded that the 4-hour period of MCA occlusion followed by reperfusion in the cat is probably too severe an ischemic insult to allow the protective effect of any agent, if such effect was only moderate, to manifest itself. We are reporting here the results of a study of the effects of Fluosol DA 20% (developed by the Green Cross Corporation, Osaka, Japan) on brain tissue oxygen availability (O 2 a), regional cerebral blood flow (rCBF), extent of brain infarction, and survival in a model of cerebral ischemia in the cat. The surviving animals were kept alive for a week for better histologic delineation of the infarct. The ischemic insult was limited to 2 hours of temporary MCA occlusion in Received December 30, 1985; accepted January 20, 1986. view of the high morbidity and mortality in our previous study with a 4-hour period of oc...