INFLUENCE OF PERFUSATE GLUCOSE-CONCENTRATION ON DIALYSATE LACTATE, PYRUVATE, ASPARTATE, AND GLUTAMATE LEVELS UNDER BASAL AND HYPOXIC CONDITIONS - A MICRODIALYSIS STUDY IN RAT-BRAIN
E. Ronneengstrom et al., INFLUENCE OF PERFUSATE GLUCOSE-CONCENTRATION ON DIALYSATE LACTATE, PYRUVATE, ASPARTATE, AND GLUTAMATE LEVELS UNDER BASAL AND HYPOXIC CONDITIONS - A MICRODIALYSIS STUDY IN RAT-BRAIN, Journal of neurochemistry, 65(1), 1995, pp. 257-262
The aim of this study was to evaluate the influence of perfusion media
with different glucose concentrations on dialysate levels of lactate,
pyruvate, aspartate (Asp), and glutamate (Glu) under basal and hypoxi
c conditions in rat brain neocortex. Intracerebral microdialysis was p
erformed with the rat under general anesthesia using bilateral probes
(o.d. 0.3 mm; membrane length, 2 mm) perfused with artificial CSF cont
aining 0.0 and 3.0 mM glucose, respectively. Basal dialysate levels we
re obtained 2 h after probe implantation in artificially ventilated an
imals. Dialysate levels of glucose were also measured for the two diff
erent perfusion fluids. The mean absolute extracellular concentration
of glucose was estimated by a modification of the no-net-flux method t
o be 3.3 mmol/L, corresponding to an average in vivo recovery of 6% fo
r glucose. Hypoxia was induced by lowering the inspired oxygen concent
ration to 3%. Hypoxia caused a disturbance of cortical electrical acti
vity, evidenced by slower frequency and lower amplitudes on the electr
oencephalogram compared with prehypoxic conditions. This was associate
d with significant elevations of lactate, Asp, and Glu levels. There w
ere no statistically significant differences in dialysate metabolite l
evels between the two perfusion fluids, during either normal or hypoxi
c conditions. We conclude that microdialysis with glucose-free perfusi
on fluid does not drain brain extracellular glucose in anesthetized ra
ts to the extent that the dialysate lactate, pyruvate, Asp, and Glu le
vels during basal or hypoxic conditions are altered.