R. Saito et al., HALOTHANE, BUT NOT ALPHA-CHLORALOSE, BLOCKS POTASSIUM-EVOKED CORTICALSPREADING DEPRESSION IN CATS, Brain research, 699(1), 1995, pp. 109-115
The effects of two anesthetics, halothane and cy-chloralose, on induct
ion of spreading depression and on extracellular glutamate elevation a
fter intracortical potassium administration were investigated in artif
icially ventilated (30% oxygen/70% nitrous oxide) cats. High potassium
concentrations were achieved using either direct KCl injections (7 mu
l, 150 mM via a micropipette) or microdialysis by supplementing 100,
300 or 500 mM KCl, respectively, for 10 min to the perfusion solution
(Ringer's). Changes of the cortical DC potential were recorded adjacen
t (1-2 mm: electrode DC1) and distant (6-7 mm: electrode DC2) to the i
njection site. Either under halothane (0.75% in the respiratory gas mi
xture) or under alpha-chloralose (60 mg/kg i.v.) anesthesia, prolonged
negative shifts of the DC potential reflecting the elevated potassium
levels after KCl injection were measured near the injection site (ele
ctrode DC1). In contrast, spreading depressions (transient short DC de
flections) were almost exclusively observed under alpha-chloralose. Sp
reading depressions recorded with electrode DC1 were superimposed on t
he prolonged negative DC shifts and they propagated frequently to the
more distant site (DC2). Upon KCl administration, dose dependent eleva
tions of extracellular glutamate were measured. These elevations were
not significantly altered by the type of anesthesia. Our results sugge
st that in cats, spreading depression induction is affected by anesthe
sia, i.e, spreading depression induction is inhibited by halothane as
compared to alpha-chloralose. Furthermore, factors other than glutamat
e or high potassium seem to contribute to spreading depression inducti
on.