Bp. Lei et al., THE EFFECT OF HYPOTHERMIA ON H2O2 PRODUCTION DURING ISCHEMIA AND REPERFUSION - A MICRODIALYSIS STUDY IN THE GERBIL HIPPOCAMPUS, Neuroscience letters, 222(2), 1997, pp. 91-94
The changes in the extracellular concentration of hydrogen peroxide (H
2O2) in gerbil hippocampus during ischemia and reperfusion were invest
igated by microdialysis coupled with fluorometry of dichlorofluorescin
oxidation. In a normothermic condition (37.5 degrees C), a transient
forebrain ischemia for 5 or 10 min produced a significant increase in
hippocampal H2O2 immediately after the start of ischemia. The duration
of this elevation after reperfusion was significantly shorter in gerb
ils subjected to 5 min of ischemia than in those subjected to 10 min o
f ischemia. Hypothermia at both 34 degrees C and 30 degrees C inhibite
d the increase in the H2O2 concentration during ischemia and reperfusi
on in gerbils subjected to 5 min of ischemia. In gerbils subjected to
10 min of ischemia, hypothermia delayed the onset of the increase in t
he H2O2 concentration and shortened the duration of the elevated H2O2
concentration. Hypothermia improved the histological outcome in the hi
ppocampal CA1 neurons 7 days after ischemia. These findings suggest th
at the suppression of H2O2 production in ischemia and reperfusion is a
possible mechanism of brain protection by hypothermia. (C) 1997 Elsev
ier Science Ireland Ltd.