De. Sakas et al., THE PERFLUOROCARBON FLUOROMETHYLOADAMANTANE OFFERS CEREBRAL PROTECTION IN A MODEL OF ISOVOLEMIC HEMODILUTION IN RABBITS, Stroke, 25(1), 1994, pp. 197-201
Background and Purpose Perfluorocarbons (PFCs) are considered promisin
g cerebral protection agents because they could combine the beneficial
effects of decreased blood viscosity with enhanced oxygen-carrying ca
pacity and oxygen tissue delivery, but trials of PFCs as hemodilutants
have been very limited. We evaluated fluoromethyloadamantane (FMA), a
new perfluorocarbon compound, as an isovolemic hemodilutant and compa
red it with low-molecular-weight dextran 40 (D40) and a control group.
Methods Through a transorbital craniectomy, the internal carotid, ant
erior, and middle cerebral arteries were coagulated to create a cerebr
al infarction in anesthetized, mechanically ventilated rabbits. No oth
er experimental procedure was performed in control animals. In the two
other groups, hemodilution was commenced 30 minutes after the arteria
l occlusion with either D40 or FMA. Hemodynamic parameters and brain a
nd systemic temperature were monitored throughout the experiments. All
animals were killed 6 hours after the arterial occlusion. Results Hem
odynamic and metabolic parameters and blood oxygen content were not af
fected by the infusion of either FMA or D40. Brain and systemic temper
ature remained constant. The ratio of infarct volume to the hemispheri
c volume was 19.6+/-3.7% in the FMA group (n=17), 19.9+/-4.6% in the D
40 group (n=16), and 40.3+/-5.7% in the control group (n=17). The diff
erence in infarct volume of both FMA and D40 animals compared with con
trols was statistically significant (P<.01) when tested with Student's
t test. There was no significant difference between FMA and D40 group
s. Conclusions These results suggest that FMA has cerebral protective
properties and should be purified, optimized, and further tested exper
imentally to develop a stable, efficient, and safe oxygen carrier, pot
entially suitable for clinical trials.