Stroke, Vol 21, 795-800, Copyright © 1990 by American Heart Association
MA Helfaer, JR Kirsch and RJ Traystman
We measured cerebral blood flow and somatosensory evoked potentials during
transient focal cerebral ischemia in cats to compare the effects of four
commonly used anesthetic regimens: ketamine/fentanyl/N2O (fentanyl),
pentobarbital, ketamine/alpha-chloralose (alpha- chloralose), and
ketamine/halothane/N2O (halothane). Six cats in each group were subjected
to 60 minutes of left middle cerebral artery occlusion followed by 120
minutes of reperfusion. Although the amplitude of the initial somatosensory
evoked potential wave complex was highest in the alpha-chloralose group
(58.6 +/- 16.5 microV) and smallest in the halothane group (27.5 +/- 5.7
microV), amplitude fell by 75% in all groups upon occlusion. Baseline
cerebral blood flow varied substantially between groups (e.g., in the right
intersylvian gyrus: fentanyl, 96 +/- 12; pentobarbital, 30 +/- 5;
alpha-chloralose, 24 +/- 3; and halothane, 76 +/- 11 ml/min/100 g).
Occlusion decreased cerebral blood flow to subcortical (e.g., left caudate)
structures in all groups (fentanyl, 29 +/- 11%; pentobabital, 45 +/- 12%;
alpha- chloralose, 27 +/- 13%; and halothane, 18 +/- 5% of baseline).
Postischemic hyperemia occurred in the cortical regions of cats
anesthetized with pentobarbital or alpha-chloralose that had reduced
cerebral blood flows during occlusion but not in cats anesthetized with
fentanyl (cerebral blood flow during occlusion not different from that of
cats anesthetized with pentobarbital or alpha-chloralose) or halothane.
After 120 minutes of reperfusion, cerebral blood flow had returned to
baseline values in all groups. Recovery of cerebral blood flow and
somatosensory evoked potential amplitude at that time did not differ among
groups.(ABSTRACT TRUNCATED AT 250 WORDS)
ARTICLES
Anesthetic modulation of cerebral hemodynamic and evoked responses to transient middle cerebral artery occlusion in cats
Department of Anesthesiology/Critical Care Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland.
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