Stroke, Vol 15, 319-323, Copyright © 1984 by American Heart Association
JR Kirsch and LG D'Alecy
When exposed to hypoxia, intact mice, with elevated blood ketones, live
longer than mice with normal blood ketones. To evaluate a possible
mechanism responsible for this phenomenon a rat brain slice preparation was
used to determine if brain tissue would utilize glucose or ketones
preferentially during exposure to reduced oxygen. Reducing available oxygen
in the incubation medium from 95%, in steps, to 5% produced the expected
gradual reduction in the carbon dioxide formation from glucose. In
contrast, reducing the oxygen level to 40 and 20% resulted in a
statistically significant stimulation of the production of carbon dioxide
from the ketone beta-hydroxybutyrate. At very low oxygen levels carbon
dioxide production from either substrate was reduced. These results are
consistent with the hypothesis that ketones can be used in addition to
glucose as a substrate for brain energy production even during reduced
oxygen availability. If the increase in carbon dioxide production from
ketones can be equated with an increase in energy production from this
supplemental substrate then ketones may be therapeutically useful in
avoiding the collapse of brain function during moderate hypoxia.
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Hypoxia induced preferential ketone utilization by rat brain slices
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