Attenuation of brain free fatty acid liberation during global ischemia: a model for screening potential therapies for efficacy?
1982
Whole brain free fatty acids (FFA) continue to rise appreciably even I h after decapitation, which may reflect the evolution of ischemic brain injury at least during global ischemia, If so, the attenuation of FFA liberation by various drugs may reflect their efficacy in ischemic brain injury. Rats were pretreated with either 0.9% NaCI (controls), ketamine, halothane, lofentanil, etomidate, Y-9179, R41-468, Innovar-Vert', pentobarbital, thiopental, or phe nytoin and decapitated 15 to 30 min thereafter. The brains were kept nor mothermic for 10 min until they were frozen in liquid nitrogen. Whole brain FFAs were quantitated by gas-liquid chromatography. After 10 min of ische mia in controls, total FFAs and arachidonic, stearic, oleic, and palmitic acids increased by 8to lO-fold. The drugs, in order of decreasing effectiveness in attenuating FFA liberation, fell into the following three groups: (1) phenytoin, thiopental, pentobarbital, and Innovar-Vet; (2) R41-468, Y-9179, and etomi date; and (3) lofentanil, halothane and ketamine. The three groups reduced total FFAs by about 23%, 13%, and 8%, respectively. The effectiveness of the drugs in attenuating FF A liberation appears to correlate with their efficacy in ischemic brain injury. However, a cause and effect relationship between FFA liberation and the evolution of ischemic brain injury must be established before accurate predictions of efficacy can be made by this method. The limitations of the proposed method of evaluation are discussed.
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