Stroke, Vol 23, 1000-1004, Copyright © 1992 by American Heart Association
M Chavko and EM Nemoto
BACKGROUND AND PURPOSE: Membrane lipid degradation plays an important role
in the pathogenesis of ischemic brain damage, but there is little
information on changes in cerebrosides, sulfatides, and sphingomyelin. We
studied regional changes in the quantities of these lipids during complete
global brain ischemia in rats. METHODS: Nitrous oxide- anesthetized rats
were subjected to ischemia by a high-pressure neck cuff and arterial
hypotension for 0 (control), 3, 10, or 30 minutes (n = 5 at each time).
Brain temperature was allowed to fall spontaneously during ischemia, and
the brain was frozen in situ with liquid N2 without recirculation. The
frontal cortex, hippocampus, and basal ganglia were dissected at -15
degrees C. The lipids were separated by column and high-performance
thin-layer chromatography and quantified by charring and densitometry.
RESULTS: Total lipid content was higher (p less than 0.01) in the
hippocampus (72.6 +/- 2.8 mg/g wet wt, mean +/- SD) than in the frontal
cortex and basal ganglia (57.7 +/- 2.1 and 62.6 +/- 1.5 mg/g wet wt,
respectively). Ischemic changes occurred only in the frontal cortex, where
total lipid content fell (p less than 0.01) by 11% after 30 minutes of
ischemia because sulfatide and cerebroside contents fell by 44% and 38%,
respectively. CONCLUSIONS: Despite a marked accumulation of free fatty
acids during complete global brain ischemia in rats, the only detectable
changes in brain lipids were in the amounts of cerebrosides and sulfatides
in the frontal cortex.
ARTICLES
Regional differences in rat brain lipids during global ischemia
Department of Anesthesiology and Critical Care Medicine, University of Pittsburgh, School of Medicine, PA 15261.
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