Mt. Alkire et al., Functional brain imaging during anesthesia in humans - Effects of halothane on global and regional cerebral glucose metabolism, ANESTHESIOL, 90(3), 1999, pp. 701-709
Citations number
27
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Background: Propofol and isoflurane anesthesia were studied previously with
functional brain imaging in humans to begin identifying key brain areas in
volved with mediating anesthetic-induced unconsciousness. The authors descr
ibe an additional positron emission tomography study of halothane's ill viv
o cerebral metabolic effects.
Methods: Five male volunteers each underwent two positron emission tomograp
hy scans. One scan assessed awake-baseline metabolism, and the other scan a
ssessed metabolism during halothane anesthesia titrated to the point of unr
esponsiveness (mean +/- SD, expired = 0.7 +/- 0.2%), Scans were obtained us
ing a GE2048 scanner and the F-18 fluorodeoxyglucose technique. Regions of
interest were analyzed for changes in both absolute and relative glucose me
tabolism. In addition, relative changes in metabolism were evaluated using
statistical parametric mapping,
Results: Awake whole-brain metabolism averaged 6.3 +/- 1.2 mg.100 g(-1).min
(-1) (mean +/- SD), Halothane reduced metabolism 40 +/- 9% to 3.7 +/- 0.6 m
g.100 g(-1).min(-1) (P less than or equal to 0.005), Regional metabolism di
d not increase in any brain areas for any volunteer. The statistical parame
tric mapping analysis revealed significantly less relative metabolism in th
e basal forebrain, thalamus, limbic system, cerebellum, and occiput during
halothane anesthesia.
Conclusions: Halothane caused a global whole-brain metabolic reduction with
significant shifts in regional metabolism. Comparisons with previous studi
es reveal similar absolute and relative metabolic effects for halothane and
isoflurane, Propofol, however, was associated with larger absolute metabol
ic reductions, suppression of relative cortical metabolism more than either
inhalational agent, and significantly less suppression of relative basal g
anglia and midbrain metabolism.