P. Hans et al., INCREASE IN ANTIOXIDANT CAPACITY OF PLASMA DURING PROPOFOL ANESTHESIA, Journal of neurosurgical anesthesiology, 9(3), 1997, pp. 234-236
We have examined the effect of total intravenous anesthesia (TIVA) usi
ng a continuous propofol infusion on the antioxidant capacity of plasm
a in 18 neurosurgical al patients who required cerebrospinal fluid shu
nting, Patients were premedicated with hydroxyzine, alprazolam, and at
ropine. Anesthesia was induced intravenously with propofol 1.5 mg kg(-
1) and sufentanil 0.15-0.3 mu g kg(-1). Tracheal intubation was facili
tated with atracurium 0.5 mg kg(-1). Anesthesia was maintained with a
continuous propofol infusion at an increasing rate from 6 to 12 mg kg(
-1) h(-1) under controlled ventilation (FiO(2) = 0.4 in air). In all p
atients, arterial blood samples were drawn before induction of anesthe
sia and during surgery for measurement of blood propofol concentration
and plasma antioxidant capacity, which was assessed as the ability to
inhibit lipid peroxidation, Lipid peroxidation was induced in vitro b
y exposing a linoleic acid microemulsion to hemoglobin-generated oxofe
rryl radicals, and assessed by ultraweak chemiluminescence in the abse
nce (central) and the presence of the plasma samples. The antioxidant
capacity of plasma, measured by the inhibition of Light emission and e
xpressed as a percentage of control, increased significantly from 39.8
+/- 2% (mean +/- SEM) to 44.7 +/- 2.4% during anesthesia (Wilcoxon te
st, p < 0.001), No correlation was observed between this increased res
istance to lipid peroxidation and blood propofol concentrations (Spear
man test, r = 0.07, NS). We conclude that the capacity of plasma to in
hibit lipid peroxidation increases in patients during TIVA maintained
with a continuous propofol infusion.