Stroke, Vol 15, 97-101, Copyright © 1984 by American Heart Association
M Sato, G Pawlik, C Umbach and WD Heiss
Functional resistance to graded hypotensive ischemia of various segments of
the somatosensory pathway was determined in anesthetized cats by repeated
concurrent recordings of regional blood flow measured by hydrogen
clearance, and evoked potentials (EPs), of dorsal horn of lumbar spinal
cord and cerebral cortex. During normal resting CNS blood flow (CBF), there
were significant successive reductions of EP amplitudes, recorded from
presynaptic spinal components (634, 424-949 microV; re-linearized mean and
95% confidence limits of log-transformed data) compared to postsynaptic
spinal (359, 247-522 microV) and presynaptic cortical (50, 32-79 microV)
and to postsynaptic cortical components (33, 22-50 microV). During ischemia
amplitudes of EPs in spinal cord and cerebral cortex showed significantly
different behaviors. The presynaptic spinal component was virtually
independent of regional blood flow down to 12 percent of resting values,
the postsynaptic cortical component exhibited strongest positive
correlations (r = 0.45) with flow. In both regions postsynaptic amplitude
was more sensitive to flow changes than respective presynaptic amplitudes.
Despite similar regression coefficients for intermediate segments of
somatosensory pathway, only postsynaptic spinal components were
significantly correlated (r = 0.40) with regional flow. Presynaptic
cortical amplitudes were variable and no significant flow dependence was
demonstrated. Results suggested that in comparable degrees of regional
ischemia of CNS functional integrity is determined by numbers of synaptic
transmissions involved locally. Comparatively simple structures, e.g. the
spinal cord, are less susceptible to ischemia and complex neuronal
networks, e.g. the cerebral cortex, are more susceptible.
ARTICLES
Comparative studies of regional CNS blood flow and evoked potentials in the cat. Effects of hypotensive ischemia on somatosensory evoked potentials in cerebral cortex and spinal cord
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